<?xml version='1.0' ?>
<source>
<publisher>ExpatJob.net Group</publisher>
<publisherurl>http://www.expatjob.net</publisherurl>
<lastBuildDate>Fri, 18 May 2012 00:00:00 GMT</lastBuildDate>
<job>
<title><![CDATA[SENIOR ESTIMATOR]]></title>
<date>Wed, 22 Feb 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob415277F76107A6CA482579AC00503C8B</referencenumber>
<City><![CDATA[Jeddah]]></City>
<Country><![CDATA[SAUDI ARABIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.expatengineer.net/jobs.nsf/v/A6CA482579AC00503C8B</url>
<company><![CDATA[Hudson]]></company>
<description><![CDATA[THE CLIENT My Client has a number of Heavy Civil Construction projects developing in the Middle East and they require a Senior Estimator to join their management team. The role will be based in Jeddah, Saudi Arabia. With a substantial portfolio of Civil Construction projects being developed this company offers the successful candidate the chance to work throughout the lucrative Middle East market.   This is a permanent staff position and the type of benefit package being awarded includes:   Competitive salary - tax free   Western style accommodation provided   x 2 paid recreation flights per annum   36 days annual leave per annum   Single or Family status   Premium Health Insurance (self and family)   Life Insurance (self)   Annual performance bonus (up to 4 months of annual salary)   End of service benefit (3 weeks per year of employment)   PURPOSE OF ROLE With a line of report to the Regional Tendering Manager and Department Head, your role will be to manage and prepare estimates for tendered CIVIL construction projects either within a specific discipline and/or as per the Clients specification and documentation. Note - there is no quantity survey aspect to this role.   MAIN RESPONSIBILITIES  Appraise and undertake detailed analysis of available tender documents and liaise within appropriate departmental stake holders   Production of estimates for the direct and indirect costs for works   Identify and undertake Risk Analysis   Produce and obtain proposals regarding work methods and equipment (including scheduling and risk analysis)   Co-ordinate with departments for specialist advise and input into the discipline related sections of the estimate   Evaluate material and sub-contract quotations in terms of cost, delivery and compliance etc.   REQUIRED SKILLS  Proven commercial skills  Proven analytical, planning and organizing skills  Communication and interpersonal skills   Capability to perform under stressful situations  Substantial knowledge of Civil Construction process   Knowledge of project costs  Knowledge of basic financial concepts   Commercial awareness   REQUIRED QUALIFICATIONS:  Degree qualified (in Engineering discipline)   If your early career has been focused on Civil Construction projects and in addition you have at least 3-5 years experience specifically as an estimator then you are encouraged to apply.   Fluent in English (written and spoken)    ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[HR Manager - West Africa]]></title>
<date>Mon, 12 Mar 2012 00:00:00 GMT</date>
<Closedate>Tue, 12 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF86407DCDDB4F128482579BF0053725B</referencenumber>
<City></City>
<Country><![CDATA[- West Africa]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.expatengineer.net/jobs.nsf/v/F128482579BF0053725B</url>
<company><![CDATA[Hudson]]></company>
<description><![CDATA[An exciting opportunity has arisen for an established HR professional to join a large scale mining operation in West Africa. With responsibility for a particular business function, the HR manager will be required to lead and mentor a team of HR professionals and specific workforce. Reporting into a HR Director, you will be an all round generalist with previous experience of working within the natural resources sector ideally in West Africa.   The position will be available on a FIFO basis with rotations typically being 7 weeks on, 3 weeks off.  Key responsibilities  Managing and guiding a team of HR professionals  Primary point of contact for all team leaders employee relations matters for on site employees Develop and implement a training and development programme across mining operations Providing training and development to a local workforce with responsibility for initiating a talent transfer between expatriate and local workforces  Responsibility for overseeing all HR Operations/Services within your business unit including HR administration and workforce/manpower planning  Key requirements  3-5 years HR management experience Previous experience of working in the extractive industries  A proven track record of building relationships with key stakeholders and managing a diverse multinational client base Ideally have experience of operating within West Africa, however wider African experience will also be suitable  A competitive salary and expatriate package is available for the suitable candidate. This is an exciting permanent position to work for a dynamic and expanding mining organisation who operate across several continents. This position will be ideal for an established HR Manager/HR Superintendent to utilise and expand their skill set and experience in a challenging environment.]]></description>
<salary></salary>
<education></education> 
<jobtype>Permanent</jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Tue, 20 Mar 2012 00:00:00 GMT</date>
<Closedate>Wed, 20 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob471E5E03862E3B96482579C70025C76A</referencenumber>
<City><![CDATA[Other]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.engineeringjobs.net.au/job/Project-Manager-3B9648.html</url>
<company><![CDATA[Anders Elite]]></company>
<description><![CDATA[FIFO on 10and4 Uplift provided Growing Contractor with Major Projects  Due to a developing pipeline of projects, this leading contractor is looking to add a Project Manager to their team to bid for projects and take them out to site. They are flexible in terms of location.  Day to day, you would be responsible for activities including general management of the project, bidding for work and tenders, liaising with clients and ensuring the project tracks appropriately.   Ideally, you will be qualified and have a minimum of four years experience managing similar projects. For this role, you will need previous Australian experience as a Project Manager on Roads projects, including some prior DMR experience.   This company has a number of projects in the pipeline and are currently tendering for more. This is your chance to get involved right from the start and make your mark on a large, notable project.  The company offers a competitive package and also some of the shorter rosters on the market. They are known for their positive work culture and ability to complete jobs on time and to budget.   Sound like the role for you? Apply now, or send your CV through to phoebe.mcdonald@anderselite.com.au. If you would like more information, please contact Phoebe on 07 3013 9509 for a confidential chat about your career aspirations. ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>4 years</experience>
</job>
<job>
<title><![CDATA[Commercial Manager/Quantity Surveyor]]></title>
<date>Tue, 20 Mar 2012 00:00:00 GMT</date>
<Closedate>Wed, 20 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDCCFA47EA1BF1E66482579C700253BA3</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Commercial-Manager-Quantity-Surveyor-1E6648.html</url>
<company><![CDATA[Anders Elite]]></company>
<description><![CDATA[A well established contractor, this company has a long history of providing innovative solutions within the industry. They have recently won a number of new contracts, and are looking for an experienced Commercial Manager to join their team in Brisbane.  As a Commercial Manager, you will: Lead, mentor and manage a large team, offering support and direction throughout the project Lead negotiation of contract terms and conditions  Review and approve contracts, variations, claims and procurement strategy  Work collaboratively across various departments Ensure appropriate risk review is carried out for all proposals Ensure corporate standards are met, including the quality of the work environment Manage and report project expenditure  Help develop and maintain key relationships with clients  To be successful for this role, you will be tertiary qualified with a degree in Quantity Surveying or Construction Management. You will have a minimum of ten years experience within the civil infrastructure sector.  In return for your efforts, you can expect to work in a supportive environment that fosters a healthy work/life balance. You will be offered a competitive salary, as well as the opportunity to grow and develop within your pre-determined career path.   If this role is of interest, please apply now, or contact Phoebe on 07 3013 9509 or via email (Phoebe.McDonald@AndersElite.com.au) to discuss this role further in confidence.   Would something similar be of interest to you or someone you know? Please have a look at our website: http://www.anderselite.com.au/, or send through a confidential CV, as we are always looking for quality candidates, including Project Engineers, Site Engineers, Contract Administrators, Commercial Managers and Project Managers.  Please note, we do not send your CV anywhere without your permission, as per the Privacy Act 1988. ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Project Engineer/Sub Agent]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8F65393D452E546C482579C80028253A</referencenumber>
<City><![CDATA[Other]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.engineeringjobs.net.au/jobs.nsf/v/546C482579C80028253A</url>
<company><![CDATA[Anders Elite]]></company>
<description><![CDATA[Top tier civil contractor  Relocate to Gladstone    Our client is a leading Contractor within the industry. With multiple offices throughout Australia, they continue to grow and add to their already notable range of projects. Due to this growth, they are now looking to add an experienced Project Engineer to their team in the Gladstone area.   As a Project Engineer, you will be involved in: Establishing and revising any design issues Overseeing quality assurance, safety compliance and programming/scheduling Watching over financial performances, as well as cost plans and forecasting Ensuring the project is tracking appropriately    To be successful for this role, you will be tertiary qualified and have a minimum of six years experience, particularly with structures and associated civil works. Previous Australian experience as an Engineer on civil infrastructure projects will be an advantage. You will also be confident with programming, overseeing trades and have good administration skills.  For your efforts, you will be rewarded with an excellent remuneration package and personal development opportunities. You can expect a supportive environment where you have a planned career path that enables you to reach your goals, along with an active social club and social sports teams.   If this role is of interest, please apply now, or contact Phoebe on 07 3013 9509 or via email (Phoebe.McDonald@AndersElite.com.au) to discuss this role further in confidence.   Would something similar be of interest to you or someone you know? Please have a look at our website: http://www.anderselite.com.au/, or send through a confidential CV, as we are always looking for quality candidates, including Project Engineers, Site Engineers, Contract Administrators, Commercial Managers and Project Managers.   Please note, we do not send your CV anywhere without your permission, as per the Privacy Act 1988. ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>4 years</experience>
</job>
<job>
<title><![CDATA[Site Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBA5B0673A79E61F3482579C800295CBE</referencenumber>
<City><![CDATA[Other]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.engineeringjobs.net.au/jobs.nsf/v/61F3482579C800295CBE</url>
<company><![CDATA[Anders Elite]]></company>
<description><![CDATA[With offices throughout Australia, this organisation is looking to build on its already thriving team. This company is known for their strong record of successful project delivery within the infrastructure, mining and energy sectors. They are currently looking for an experienced Site Engineer to join their team in Gladstone.   As a Site Engineer, you will: Ensure the successful delivery of the project on time, within budget and to the required quality standard Provide general technical assistance and interpret engineering documents  Providing technical support and reporting phases of the project  Maintaining systems and performing certain evaluations  To be successful for this role, you will be tertiary qualified and have a minimum of three years experience within the roads and earthworks sector. Experience in a similar role on projects involving earthworks will be considered favourably, as will previous experience within a Top or Mid Tier Civil Contractor and a strong understanding of QA and OHandS.   In return for your efforts, you can expect a competitive salary package along with opportunities for growing and developing your career. Our client also offers a supportive work environment and facilities to support a healthy lifestyle.   If this role is of interest, please apply now, or contact Phoebe on 07 3013 9509 or via email (Phoebe.McDonald@AndersElite.com.au) to discuss this role further in confidence.   Would something similar be of interest to you or someone you know? Please have a look at our website: http://www.anderselite.com.au/, or send through a confidential CV, as we are always looking for quality candidates, including Project Engineers, Site Engineers, Contract Administrators, Commercial Managers and Project Managers.  Please note, we do not send your CV anywhere without your permission, as per the Privacy Act 1988. ]]></description>
<salary></salary>
<education>None</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>1 years</experience>
</job>
<job>
<title><![CDATA[Engineering Manager - Hydraulics]]></title>
<date>Sun, 22 Apr 2012 00:00:00 GMT</date>
<Closedate>Sun, 22 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob947D36B4D59A2F3D482579E8004D12FB</referencenumber>
<City><![CDATA[Dammam]]></City>
<Country><![CDATA[SAUDI ARABIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.expatengineer.net/job/Engineering-Manager---Hydraulics-2F3D48.html</url>
<company><![CDATA[AFI]]></company>
<description><![CDATA[We are a leading engineering company engaged in the manufacture, service and repair of hydraulic, pneumatic and related products based in Dammam, Saudi Arabia. Our products and services are sold into a range of sectors including, including oil and gas, transportation, construction and manufacturing.  We are currently seeking an experienced engineering manager to lead our team of design engineers and to assist the companys growth into new technological sectors.   Reporting to the General Manager, the ideal candidate should have:   Degree in Mechanical Engineering, or related discipline  A post graduate qualification in project or business management is desirable   Minimum 15 years engineering experience, where the last 5 years have been in a managerial role  Extensive experience in hydraulics engineering is a prerequisite for this position   Experience in pneumatics, steel fabrication, fluid conveyance is desirable.   Good working knowledge of designing for manufacture including related processes and procedures   Experience with regulatory systems such as ISO 9000, ASME and API is desirable     Excellent people management and leadership skills  Good communications, planning and presentation skills   Excellent command of English, both written and verbal  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[DDON  RN]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob87E528C7C810BEEF482579E9001D071F</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/DDON-RN_1604084.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Fully Accredited Aged Care Facility Excellent Salary Package Professional Development and Career Progression We are looking for a Registered Nurse for a Deputy Care Manager role within a state-of-the-art Aged Care facility on the Gold Coast. Our Client is a leading Aged Care provider, offering excellent career progression and ongoing professional development for their employees.  Reporting to the Director of Nursing, you will be responsible for supporting the nursing team, delivering exceptional patient care and assisting with training and education. You will add value through your leadership skills and extensive clinical knowledge.   To be considered for this exciting opportunity, you will have; Current AHPRA registrationExperience within Aged Care  Understanding of accreditation and ACFIBe flexible, approachable, confident and a resourceful individualStrong communication skills and the ability to converse at all levels On offer is an excellent salary package, a true career progression, ongoing training and support to excel in your role.     To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN506.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[DON  Care Coordinator RN]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF1FC54AEE99F3845482579E9001D0753</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/DON-Care-Co-ordinator-RN_1604144.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Aged Care Management Position Excellent Salary Package Supportive structure, facility and working environment Located in the Central Coast our Client is seeking a DON / Care Co-ordinator  (Registered Nurse) who is focussed on providing the highest level of care to residents whilst positively leading the team. You will be responsible to provide leadership to maintain a successful, person centred approach to care, and ensure compliance with all aspects of Aged Care Standards.  This role is suited to an experienced Aged Care Manager, or a motivated and experienced Registered Nurse looking to take that next step into management, who enjoys a challenge that this position brings.   To be considered for this exciting opportunity, you will have; Current AHPRA registrationExperience within Aged Care  Understanding of accreditation and ACFIBe flexible, approachable, confident and a resourceful individualStrong communication skills and the ability to converse at all levels On offer is an excellent salary package, a true career progression, ongoing training and support to excel in your role.  Other roles available for RN s and Aged Care Managers please get in touch if you would like to hear more.     To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN507.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Project Manager  Commercial Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob298E0283F3758BA8482579E900236F7B</referencenumber>
<City><![CDATA[Como]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Project-Manager-Commercial-Construction_1604139.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an innovative construction company operating in the commercial and industrial sectors of QLD and WA. They are known for specialising in the completion of prestigious commercial construction projects from design through to hand over, managing all aspects of the commercial construction process.     Due to an increase in workload, our client is now looking for a Project Manager to join their team in Como.     The role and responsibilities of the Project Manager will include, but not be limited to;    Submitting VariationsDocument flow distributionManagement and coordination of subcontract and supplier agreementsMaintaining and managing all incoming and outgoing contractual correspondenceProviding comprehensive support for all contract administration processes with a view to developing a systematic standard for all projectsProvide support in claim management and documentation including variation management, reporting and contract entitlements;Prepare procurement documentation ensuring that suppliers, subcontractors and consultants are fully aware of their obligations for project deliveryReview, as appropriate, non compliance reports which may have an impact on the contractWork with Project Managers to accurately forecast costs and incomeSub-contract documentation preparationManagement of head contractManagement of sub-contracts    The ideal candidate for this role will have previously worked for a commercial building and construction contractor in Australia and holds a degree in Construction Management and Economics.     In order to be successful, candidates will need to display; A degree in Construction Management, Quantity Surveying, Economics or similar or currently studying;Up to 5 years experience in a similar roleHave excellent communication skills, both written and verbal;Good analytical and strategic thinking capabilities;Excellent problem solving abilities;An excellent commercial focus and well developed commercial acumen    This position offers a competitive remuneration package, challenging work and excellent career development.  Australian experience essential.  If you are ready to join a reputable company south of the river APPLY now!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Environmental Advisor  QCLNG  Gas Pipeline Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob30FD65766F872D0B482579E900236FC7</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Environmental-Advisor-QCLNG-Gas-Pipeline-Construction_1604249.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[    Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  Due to current project requirements, they are now seeking an Environmental Advisor to provide assistance to the Environmental Manager on the QCLNG project, one of Queenslands biggest pipeline construction projects.  You will be reporting to the Environmental Manager and your main responsibility would be to maintain safe environmental practices around the site.  This is a site-based, FIFO position: candidates will fly to site located between the Surat Basin and Gladstone on a rotation of 28 days on and 9 days off.  While on site, your responsibilities will include (but not be limited to); The inspection, monitoring and provision of advice relating to construction activities to ensure compliance with Environmental obligations in accordance with the Construction Environmental management Plan.Ensure that planned controls for environmental aspects of works areas are met in accordance with the construction teams Work Method Statements (WMS), the project CEMP or Environmental Protection Instructions (EPIs).Report to the Environmental Manager or Coordinator of any potential or actual environmental aspect or impact.Review, instruct, record, and report all environmental matters relating to any given works area of the project.Function as the field environmental representative and conduit of Environmental Management Team.Compliance with the Environmental Responsibilities. We are looking for candidates who are able to demonstrate: Trades qualification or experience relevant to the construction, building or manufacturing industriesSound working knowledge of Environmental requirements and implementing of the sameStrong team management skills and good oral and written communication skills. This is a permanent, long-term, site-based, FIFO position and candidates must be prepared to work a rotation of 28 days on and 9 days off. Travel and meals are provided and each candidate will have an individual ensuited room.  If you are looking for a role that is different, yet essential within the team, then apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Officer  Electrical drafting]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob782077440B522924482579E900237015</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.expatengineer.net/job/Technical-Officer-Electrical-drafting_1604251.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Officer, with an electrical background to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsAssist engineers with design of HV/LV plant.Assist in the development of technical documents, specifications and manualsHelp with proposalsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleDiploma in Engineering or Electrical Licence is desirable.Experience in power distribution and drives (LV/HV).Development and review of electrical design deliverables (SLDandrsquo;s / schematics / GAandrsquo;s / schedules).Exposure to an industrial engineering environment or office.Exposure to electrical drafting.Experience in electrical design and drawings. If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Electrical Designer  Engineering]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob457D612EE15FD79B482579E90023703F</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Lead-Electrical-Designer-Engineering_1604252.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking an experienced Lead Electrical Designers to join the Brisbane team. Drafting diploma or equivalent, specialising in ElectricalAdvanced knowledge of Australian Design Codes and Standards. Intermediate knowledge of MS Excel and Word. 15+ yearsandrsquo; experience in Electrical design drafting within an industrial environment. Brownfield/Greenfield Project Experience.Mining/Hydrocarbons experience EssentialProven experience in similar role    The company is actively expanding and is seeking applicants for the role of Lead Electrical Designer based in the Brisbane office. Full time, contract or casual employment arrangements will be considered for this role. Donandrsquo;t miss this excellent opportunity, please send your application through now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Control Systems Engineer  Mining in Mackay]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDD0992E2E7094D1B482579E90023705D</referencenumber>
<City><![CDATA[Mackay]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Control-Systems-Engineer-Mining-in-Mackay_1604253.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in Mackay. The ideal candidate for this role will be someone who has a reliable level of experience in design and project management within the mining and resource industry. You should now be at a level where your management skills are well developed, or you are now ready to expand into this responsibility.     The role of the Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.  The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportExpereince working in Regional Areas5 years industry experience in the Australian market The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; OIS programming and testingElectrical engineering including designProject management activities    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electrical Engineers   Hazardous Area]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD38777EC0F27419E482579E90023707A</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Senior-Electrical-Engineers-Hazardous-Area_1604254.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[  Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth, development and on-going work, they are currently seeking highly experienced Electrical Engineers from the Oil andamp; Gas and Hydrocarbon industries, who have a strong knowledge of the Hazardous Area. Opportunities exist in both Perth and Brisbane.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and GasDegree or equivalent experience/qualificationsExperienced with Hazardous Area Technical writing and design specification experience Experienced with High Voltage     The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.Produce electrical designs as required.In addition produce instrumentation and control systems designs as required.Carry out electrical testing and associated electrical installation works as required:In accordance with the relevant legislation, and Within the employees competencyAs authorised by the Employer, andSo as to meet project requirements    We are looking for candidates who are able to display at least 5 years experience in Electrical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! Australian experience is necessary! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer  Control Systems in Mining & Minerals]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F1A38F52FC31E9F482579E9002370A4</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Project-Engineer-Control-Systems-in-Mining-and-amp-Minerals_1604255.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth and development, they are currently looking for an experienced Project Engineer to join their team in West Perth. Candidates are required to have had some experience in the Mining and Minerals industry and you will be required to provide technical deliverables of a project using your background in Control Systems Engineering.     The successful applicant will also have Proven Technical skills in: Control Systems EngineeringPLC andamp; OIS programming and testingElectrical engineering including designProject management activitiesDiscussions with various stakeholders (site operational people to extract information)Project Engineering through implementation phases of the projectTechnical / Report Writing    You will also be required to assist in the control and monitoring of schedules and financial aspects of a project with the team in liaison with the Project Manager.     We are looking for candidates who are able to display at least 5 years experience in a project engineering role and mining industry experience will be highly regarded.     The role of the Control Systems Engineer will also be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical)High end computer literacyWell developed written and verbal communication skillsSite Commissioning experienceProven record in site support5 years industry experience in the Australian market    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Process Engineer  Mining]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob502C6ACE32C21ACD482579E9002370CA</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[West Australia]]></State>
<url>http://www.expatengineer.net/job/Process-Engineer-Mining_1604256.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.    Due to growth, development and project demands, they are currently seeking a Process Engineer for a 12 contract. In order to be successful, the candidate will need:  Degree QualifiedMinimum 3 years experienceIron Ore (mining and minerals) experienceBrownfields experienceGood understanding of Australian standards    Your responsibilities will include but not be limited to:    Feasibility studiesSite work when requiredEngaging with clientsDesign conceptual studies       This is an outstanding opportunity for an experienced scheduler to further their resources experience with an Australian company that encourages career growth. This is a varied role and your chance to demonstrate your skills in a highly respected EPCM company. If you believe you meet the required skills and you are looking for the next challenge in your career, we welcome your application.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Mechanical Engineer  Oil & Gas  Hydrocarbon]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4F2009605056FB67482579E900237113</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[VICTORIA]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Mechanical-Engineer-Oil-and-amp-Gas-Hydrocarbon_1604258.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking highly experienced Mechanical Engineers who have experience in the Oil andamp; Gas and Hydrocarbon industries, to join the growing team in Melbourne.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and Gas / Hydrocarbon IndustriesDegree or equivalent experience/qualificationsExperience in Engineering from FEED, Detail to Project DeliveryTechnical writing and design specification experience Australian experience    The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.       We are looking for candidates who are able to display at least 5 years experience in Mechanical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Control Systems Engineer  Mining & Resources]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB1D1AD73692C368482579E900237133</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Lead-Control-Systems-Engineer-Mining-and-amp-Resources_1604259.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in West Perth. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer.  The role of the Lead Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 5 years industry experience in the Australian market Candidates will be required to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Provision of technical guidance to junior engineers and peers;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts.    The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activities    We will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Business Development and Exploration Manager  Perth based]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9436ED5B8DE76CD3482579E900237151</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Head-of-Business-Development-and-Exploration-Manager-Perth-based_1604260.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Business Developer, all Exploration activities both regional as well as near mine, and the Corporate Mine Geology function.  Based in the Perth CBD you will be reporting directly to the CEO. You will be accountable for the Business Development, all Exploration activities (both regional and near mine), and the Corporate Mine Geology Function. You will manage a technical team which will focus on delivering effective exploration plans, improving and expanding the Groups business through the optimisation of existing operations and identification of new development or acquisition opportunities.     The duties and responsibilities for this role are as follows; Promote safety awareness in the department as well as contributing to the maintenance and review of procedures and work practices,Ensure support and compliance with all rules and regulations, statutory compliance, company policies, and procedures,Contribute to mine geology budgeting processes, including manning levels and drilling requirements,Plan, budget, Implement and manage suitable exploration programs through to pre-feasibility stage ensuring the highest standard of safety and environmental management,Participate in the provision of reports in timely manner with accurate Geological information,Establish and maintain relationships with government agencies, community groups, and other stakeholders including landowners and indigenous groups. To be successful in this role, you must possess the following as a minimum; Must have Tertiary qualifications in Geology or related subjects,Minimum 15 years experience, largely in metal base exploration and mining,Proven and demonstrated experience in leading and supervising a technical team,Operating experience both in open pit and underground environment,Previous experience in project evaluation and financial modelling,Experience in dealing with resources industry corporate matters,Competency in mining software packages (Surpac and Datamine preferred), Microsoft Office, GIS Packages (Mapinfo or ArcView),Demonstrated commitment and support of Company Values and Behaviours. With attractive salary packages and incentives on offer it is an opportunity not to be missed. If this job sounds like its the right one for you then please apply.          ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Exploration and Production</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Assistant  Engineering]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAFC705187A899D07482579E900237176</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Technical-Assistant-Engineering_1604261.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Assistant to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsHelp with proposalsAssist with invoicingAssist with writing technical dcuments and manualsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleA relevant qualification would be advantageousExcellent MS office skillsTechnical/Electrical drafting backgroundGood organisational and administrative skillsBe a team playerEnjoy a busy work environment If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal & Lead Process Engineers  Mining & Minerals]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDF6D301AB76CEA35482579E900237194</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[South Australia]]></State>
<url>http://www.expatengineer.net/job/Principal-and-amp-Lead-Process-Engineers-Mining-and-amp-Minerals_1604262.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking to engage a Principal and Lead Process Engineers , to become part of the team that coordinates the technical development and assist the commercial team in the development of Greenfield and Brownfield projects through pre-feasibility / feasibility studies. This is a permanent, full time role in Adelaide.     Our client is seeking personnel at various levels of their engineering degrees.     The Person  The successful candidate will ideally have the following qualifications and experience:     Bachelor of Engineering A minimum of 6 years experience as a Process Engineer Mining andamp; Hydrocarbons industry experience Pre-feasibility/Feasibility study work.     Your responsibilities may also include, but will not be limited to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts; andFor the more senior candidates; a provision of technical guidance to junior engineers and peers.       We are looking for candidates who have a well developed understanding of the Mining and Mineral Processing industry.  If this sounds like you then please apply now!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Structural Designer  Oil and Gas]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6C731A265AC322F3482579E9002371B3</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Structural-Designer-Oil-and-Gas_1604263.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.     Due to ongoing work and an increase in demand, they are now seeking an experienced Senior Structural designer to join their team in Perth who are working on an onshore gas plant in Western Australia. Candidates should have a high level of experience in the oil and gas industry and ideally have the following qualifications and experience: Minimum eight years relevant experienceExperience using AutoCAD Version 11 or Autoplant v8iHighly developed technical skillsAbility to work in and manage a small teamCivil and Structural designDemonstrated design experience in Oil andamp; Gas / Hydrocarbon industry experience preferredAustralian experience essentialAustralian citizenship or permanent residency essential The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the oil and gas industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pipe Stress Engineer  Mechanical & Piping Engineer   Onshore Oil and Gas]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4D48F00E28958DF3482579E9002371D0</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Pipe-Stress-Engineer-Mechanical-and-amp-Piping-Engineer-Onshore-Oil-and-Gas_1604264.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.     Due to ongoing work and an increase in demand, they are now seeking an experienced Mechanical andamp; Piping Engineer with Pipe Stress Engineering experience to join their team in Perth CBD. We are looking for candidates who have experience working on onshore gas plants in Australia.     We are seeking Mechanical Engineers who have a high level of experience in the oil and gas industry and the successful candidate will ideally have the following experience: Piping stress analysis experience in a Consulting / Engineering environment pertaining to Hydrocarbon / Petro-chemical / Oil andamp; Gas sectors.In-depth knowledge in stress analysis and using Caesar IIAdequate knowledge in Piping layout, Design of Supports, Hanger selection etc.Knowledge of dynamic analysis will be considered an added advantage. In order to be successful, candidates will also be required to experience on:    Plot Plans, Piping Layouts,Piping Specifications, Valve specificationsStress AnalysisVendor quote evaluationsVendor quote evaluationsVendor drawing review and approval    In order to be successful, candidates will be required to; Mechanical Engineering DegreeMinimum of 5 years in a similar roleCommercial awareness for project evaluation and submission for approvalClear and respectful communication skills at all levelsHighly developed time and task managementGood understanding of Australian codes and standards    The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the downstream oil and gas industry.     If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Spotter Catcher  QCLNG Project  Gas Pipeline Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE57E6DF30E16E89D482579E9002371F5</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Spotter-Catcher-QCLNG-Project-Gas-Pipeline-Construction_1604265.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[    Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  Due to current project requirements, they are now seeking the assistance of three experienced Spotter Catchers/Fauna Handers to relocate and document fauna on one of Queenslandandrsquo;s biggest pipeline construction projects.  You will report to the Environmental Manager and aside from relocating and documenting fauna from the project site, you will promote environmental awareness to all persons in the job vicinity and assist with the development of environmental training and monitoring programs.  This is a site-based, FIFO position: candidates will fly to site located between the Surat Basin and Gladstone on a rotation of 28 days on and 9 days off.  While on site your responsibilities will include (but not be limited to); Relocate arboreal and avian faunal species and any terrestrial fauna caught inside trench andamp; excavations.Document type andamp; number of species relocated from the RoW or from trench or excavations.Respond to any supervisor request to relocate fauna from works areas.Report to andamp; follow direction given from the Environmental Manager or coordinator.Responsible for preparing Fauna reports monthly and summary report upon completion of works.Assist in the development andamp; implementation of monitoring programs and environmental training / toolbox topics.Report to the Environmental Manager or Coordinator of any potential or actual environmental aspect or impact.Compliance with the Environmental Responsibilities. This is a permanent, long-term, site-based, FIFO position and candidates must be prepared to work a rotation of 28 days on and 9 days off. Travel and meals are provided and each candidate will have an individual room with ensuite.  In order to be successful it is essential that the candidates have; Relevant experience as deemed by Western Pipeline Alliance, Peers and Environmental Manager.Sound working knowledge of Environmental requirements and implementing of the same.Exceptional vigour and energy accompanied by good oral and written communication skills.Snake Rehabilitation PermitAbility to Hold a Damage Mitigation Permit. If you are looking for a role that is different, yet essential within the team, then apply now!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[AGED CARE RN  CARE MANAGER]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0892FA120B48AAF4482579E9002DAC1E</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/AGED-CARE-RN-CARE-MANAGER_1604231.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Progressive Aged Care Organisation Excellent Salary Package and Career Prospects Sought after role in delightful facility THE ROLE:  Progressive Aged Care organisation with great career prospects, offering a delightful working environment. Reporting to the Facility Manager your duties are varied and interesting, assisting in managing the overall operations of the Facility. You will be an integral and respected member of the team, as this role is well supported within a very well run facility.      Assist the Manager to ensure the smooth operation of the facility.   Oversee clinical assessment, care planning, and ACFI funding    Lead and mentor the dedicated care team   Ensure compliance to the Aged Care Legislation and Accreditation Standards    Training and development of staff    Rostering     ABOUT YOU:  We are seeking a dedicated RN, with management experience or the desire to take that next step. Aged Care experience is a plus, along with knowledge of ACFI and Accreditation. You must have strong communication skills and the ability to converse at all levels, you are flexible, approachable and resourceful.   This is an amazing opportunity not to be missed, a rewarding job where you will be respected for your work within a caring and supportive environment. An excellent salary is on offer, and the chance for true career progression.     To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN5012.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[RN's for permanent roles in Wollongong and Southern NSW.]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC9FB79CBE0C4D5D3482579E9002DAC3B</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/RN-and-SHARP039s-for-permanent-roles-in-Wollongong-and-Southern-NSW_1604327.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Excellent career step with on-going training Leading NFP organisation Generous salary package We require enthusiastic and motivated Registered Nurses to join a Leading NFP Aged Care Provider offering great working conditions, flexibility, career progression, competitive wages and salary packaging benefits.  Full Time permanent positions available.  A range of shifts available from Mornings to Afternoons and Night Duty.  Job Summary:  This exciting role will see you working as a team-leader alongside a dedicated care team drawing on your knowledge and experience.  You will monitor and deliver care in accordance with nursing plans and professional practice standards. Your well developed judgment will enable you to perform your duties, and your strong interpersonal skills will ensure that the emotional and physical comforts of residents are met. You will confidently direct staff involved in resident care, and manage stressful situations with poise and professionalism. You are committed to quality and exceptional care.  You must have:  Registration with AHPRADemonstrated clinical experience / skillsAged Care experience highly regarded, however not essentialExcellent organisation and communication skills Don t miss this opportunity for true career progression, working in a supportive environment that respects you and your skills, offering fantastic rewards and job satisfaction. Apply now!!     To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN5013.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[RN's for permanent roles in Newcastle and Hunter]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD27C8E47C4753273482579E9002DAC98</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/RN-and-SHARP039s-for-permanent-roles-in-Newcastle-and-Hunter_1604331.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Excellent career step with on-going training Leading NFP organisation Generous salary package We require enthusiastic and motivated Registered Nurses to join a Leading NFP Aged Care Provider offering great working conditions, flexibility, career progression, competitive wages and salary packaging benefits.  Full Time permanent positions available.  A range of shifts available from Mornings to Afternoons and Night Duty.  Job Summary:  This exciting role will see you working as a team-leader alongside a dedicated care team drawing on your knowledge and experience.  You will monitor and deliver care in accordance with nursing plans and professional practice standards. Your well developed judgment will enable you to perform your duties, and your strong interpersonal skills will ensure that the emotional and physical comforts of residents are met. You will confidently direct staff involved in resident care, and manage stressful situations with poise and professionalism. You are committed to quality and exceptional care.  You must have:  Registration with AHPRADemonstrated clinical experience / skillsAged Care experience highly regarded, however not essentialExcellent organisation and communication skills Don t miss this opportunity for true career progression, working in a supportive environment that respects you and your skills, offering fantastic rewards and job satisfaction. Apply now!!     To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN5014.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Inspector (Civil)  Gas Pipeline Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob09CCD8A43FDA5982482579E90039E065</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Quality-Inspector-Civil-Gas-Pipeline-Construction_1604356.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Engineering, Construction, Building and Maintenance Company with a global presence. Their expertise is based on complex infrastructure projects in a number of sectors and they have ongoing projects throughout the Australasia region.  Due to current project requirements, they are now seeking the assistance of a Quality Inspector to perform inspections and surveillance upon receiving, during and post installation of all civil related products and construction.  This is a site-based, FIFO position: candidates will fly to site located between the Surat Basin and Gladstone on a rotation of 28 days on and 9 days off.  Whilst on site your responsibilities will include (but not be limited to); Conduction of Receiving Inspection, In-Process Inspection and Final Inspection of civil related products and constructionCoordinating with civil departments in matters related to inspectionImplementation of inspection and test plan including witness and hold pointsCompleting and signing inspection reportsInspection of earthworks including compaction tests and materialsInspection of reinforcing bars including embedded itemsInspection of concrete works including checking sampling process and testingChecking compression test results and curing process of concrete structuresConducting final inspection of concrete structures In order to be successful it is essential that candidates are able to demonstrate; Relevant Tertiary QualificationsExperience in same or similar positionFamiliarity with applicable code requirements (ACI Code and ASTM)Experience reviewing specifications and drawings Candidates will also need to have sound interpersonal skills as they will be dealing with customers and other civil departments.  This is a permanent, long-term, site-based, FIFO position working on the QCLNG project. Candidates must be prepared to work a rotation of 28 days on and 9 days off. Travel and meals are provided and each candidate will have an individual room with ensuite.  If you are analytically minded, good with time management and looking for a role that is different, yet essential within the team, then apply now!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QC Inspector (Fabrication)  QCLNG  Pipeline Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34267B5B3EC4CDC8482579E90039E120</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/QC-Inspector-Fabrication-QCLNG-Pipeline-Construction_1604357.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  Due to the start of a large Gas Pipeline Construction project, they are seeking an experienced Fabrication QC Inspector to partake in inspection at 3rd party fabrication facilities. It will be highly advantageous if candidates have had experience working within the Oil and Gas Construction industry.  This position is Fly-in Fly-out (FIFO) or Drive-in Drive-out (DIDO) to 3rd party fabrication facilities located outside of Bribane, QLD for a rotation of 28 days on and 9 days off.  Key Responsibilities will include (but not be limited to): Assuring that the manufacturer has acceptable inspection and test techniques and procedures that are being adhered to, and documentation completed.Reviewing and signing the completed manufacturerandrsquo;s data report.Verifying the following aspects:Welders engaged in the fabrication are certified Materials used in fabrication comply and have the required test reports or material certification.Specified welding procedures are being used.Weld preparations, shape, fit-up and cleanliness of parts comply.Production test welds are carried out and the results are acceptable.Defects repaired by welding have been acceptably repaired. The required non-destructive examinations and other tests have been performed and the results are acceptable. In order to be successful the candidate will need to demonstrate: Experience in the fields of Fabrication Inspection (QC) and Welding of Oil and Gas Pipelines.Conversant with Australian StandardsExperience on oil and gas construction projects preferably with Pipelines  To be successful, candidates will require experience in a similar capacity within a consultancy or contractor, preferably within the oil andamp; gas construction or EPCM industries and Australian experience is essential.  This role will require candidates to be highly conscientious of quality standards. An ideal candidate will have high attention to detail, will be able to identify and eliminate fabrication flaws and defects, while helping to maintaining the highest level of integrity and compliance.  This is a permanent, long-term, site-based, FIFO position working on the QCLNG project. Candidates must be prepared to work a rotation of 28 days on and 9 days off. Travel and meals are provided and each candidate will have an individual room with ensuite.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QC Inspector (Received Materials)  QCLNG  Pipeline Construction]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7BA6C525A2E7B193482579E90039E15A</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/QC-Inspector-Received-Materials-QCLNG-Pipeline-Construction_1604358.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  Due to the start of the QCLNG project, a large Gas Pipeline Construction project, they are seeking an experienced Received Materials QC Inspector. It will be highly advantageous if candidates have had experience working within the Oil and Gas Construction industry.  This is a site-based, FIFO position: candidates will fly to site located between the Surat Basin and Gladstone on a rotation of 28 days on and 9 days off. Travel and meals are provided and each candidate will have an individual room with ensuite.  Key Responsibilities will include (but not be limited to): Checking received items against the purchase order request.Perform required inspections and tests.Review vendor documentation and test data for compliance and completeness.Prepare and then file all required receiving inspection documentation.  In order to be successful the candidate will need to demonstrate: Experience in the fields of Inspection (QC), NDT, and Welding and materials control of Oil and Gas Pipeline parts.Conversant With ASTM Standards, API and ASMEConversant with ISO 9001: 2000 Quality System Experience on oil and gas construction projects preferably with Pipelines    To be successful, candidates will require experience in a similar capacity within a consultancy or contractor, preferably within the oil andamp; gas construction or EPCM industries and Australian experience is essential.  This role will require candidates to be highly conscientious of quality, customer service and inventory levels. An ideal candidate will have high attention to detail, strong communication skills and will be able to work under pressure to meet tight deadlines.  This is a permanent, long-term, site-based, FIFO position working on the QCLNG project. Candidates must be prepared to work a rotation of 28 days on and 9 days off. This is a salary based position, contractors need not apply. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Mining Engineer  Underground Mining]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD6BCC84443EAACF8482579E90039E180</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Senior-Mining-Engineer-Underground-Mining_1604567.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Mine Planning Engineer to join their diverse team.  Based at their Pilbara operations, this is a permanent FIFO position on a 86 roster. You will be reporting to the Chief Mining Engineer and your main responsibility will be to prepare medium to long term mine designs, activity schedules and production schedules in and around the operation.  Your responsibilities will include; Prepare mine designs with specific attention to optimisation of development and mining method, provision and optimisation of exploration and delineation drilling sites, maximisation of economic return from geological resource,Accurately address all relevant aspects in designs and schedules including development, stoping, ground support, rock mass stability, backfill, ventilation, mine dewatering, materials handling, power supply and reticulation, water supply and reticulation and communication and data transfer,Prepare the annual ore reserve estimate,Contribute to production performance record keeping and reporting,Program, monitor and record the activities of the Mining Contractor,Develop, maintain and improve sectional systems and procedures,Ensure adherence to all statutory requirements and company safety, health and environmental standards and procedures,Identify and investigate opportunities and methods for reducing unit production costs and maximising output.    In order to be successful with this role, you will be required to have; Tertiary qualifications in Mining EngineeringAt least five yearsandrsquo; experience in Underground mechanised mining,Ability to write and deliver reports, presentations, business correspondence, reviews and other materials,Ability to diagnose issues, establish plans and determine priorities to achieve objectives,Commitment to quality, teamwork, innovation and achieving results,Ability to meet deadlines and flexibility approach to problem solving, priority setting and time management,Strong professional interpersonal skills and ability to communicate skills at all levels.    If this sounds like a good opportunity for you, then please apply now.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Mine Geologist  Pilbara Operations]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF7717BF28836956B482579E90039E1B6</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Senior-Mine-Geologist-Pilbara-Operations_1604568.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD.     Due to current expansions and restructuring, our client is currently seeking an experienced Mine Geologist.     This is a permanent position with a Fly-In-Fly-Out roster of 8 days on, 6 days off roster to the West Australian operation.     The primary role of the Mine Geologist is to provide management and administration of the geology department and its function on site. The successful candidates will report to the Geology Manager.     The duties and responsibilities for this role are as follows;    Provide the necessary management skills to achieve optimum mine production performance through accurate resources estimation, accurate grade control and recording. Contribute to the effective management and administration of the mine site exploration activities through near mine evaluations, organisation of onsite logistical support and statutory report delivery. Provide regular contributions to the daily, weekly, monthly and annual reportsAssist with ground control, dewatering, mining engineering/planning and survey requirements Provide technical and management support for the site management teamAssisting with environmental requirements Constantly promoting a team and cooperative approach within the department       To be successful in this role, you must possess the following as a minimum Degree in Geology Minimum of 5 years experience in the mining industry- within open pit/underground environment Strong management skills and ability to work as part of teamAbility to work without supervision Possess professional written, verbal and presentation skills,Possess professional and good communications and interpersonal skills,    With attractive salary packages and incentives on offer it is an opportunity not to be missed. If this job sounds like its the right one for you then please apply.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Drill & Blast Engineer  Underground Mining]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob746E30401A6671B2482579E90039E1DF</referencenumber>
<City><![CDATA[Mt Gordon]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Drill-and-amp-Blast-Engineer-Underground-Mining_1604569.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Mine Planning Engineer to join their diverse team.  Based at their Northern QLD operation, this is a permanent FIFO position on a 86 roster. Reporting to The Production Superintendent you will be required to prepare drill and blast designs as well as to plan and schedule in accordance with the mine requirements.  The Responsibilities Provide stope drill and blast designs in a timely manner for stoping blocks,Maintain quality assurance standards and practices by conducting audit checks and inspections of drilling and blasting requirements,Collection, collation and reporting of mine physical data on a daily basis,Update all plans and weekly production schedules and graphs and any other relevant performance monitoring measures on a daily basis,Ensure continuous improvement by liaising with operators and Supervisors for practical plans,Prepare short term production, long hole drilling and development schedules,Data maintenance including cost control and budget,Training and mentoring staff if required. The Requirements Must have tertiary qualifications in Mining EngineeringAt least five years experience in Drill and Blast in Underground Mining environment,Competency with use of Microsoft Office, Surpac and Ring King software,Ability to write and deliver reports, presentations, business correspondence, reviews and other materials,Ability to diagnose issues, establish plans and determine priorities to achieve objectives,Commitment to quality, teamwork, innovation and achieving results,Ability to meet deadlines,Strong interpersonal skills and ability to communicate skills at all levels.    If you are looking for a great opportunity in 2012, then please send your resume! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Ventilation Engineer  Underground Mining]]></title>
<date>Mon, 23 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 18 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9E7EF02675300E6A482579E90039E262</referencenumber>
<City><![CDATA[Mt Gordon]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Ventilation-Engineer-Underground-Mining_1604570.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD.  Due to current expansions and restructuring, our client is currently seeking an experienced Ventilation Engineer to join the team in their Queensland operations.     Reporting to the Chief Mining Engineer, this role is a permanent Fly-In-Fly-Out position on an 8 days on/6 day off roster. The position requires close liaison with the underground mining contractor and specialist consultants, where required.     The Responsibilities;    Maintain currency with latest ventilation regulations, techniques and methods.Maintain currency with latest mining technology, equipment and regulations.Assist with the Management of all Mining Contractors on site to ensure adherence with contractual agreements and operational requirements.Conduct ventilation surveys of primary and secondary systems and record all results.Prepare, update and distribute all quarterly ventilation plans.Maintain optimum air quality and heat measurements.Achieve budget physical and cost targets for primary and secondary ventilation activities.    The Requirements;    Degree qualifications in Mining EngineeringFive years experience in underground metalliferous mining.One years experience in ventilation engineering in underground metalliferous mining.Sound competency with computer use and Microsoft Office.Commitment to quality, teamwork, innovation, achieving objectives and outcomes.Ability to meet deadlines, Flexible approach to problem solving, priority setting, and time management.Strong interpersonal skills; verbal and written communication skills    If this sounds like a good opportunity for you then please apply now. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Electrical Maintenance Engineer]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 24 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4B5119A4F78B1EE6482579E90083329E</referencenumber>
<City><![CDATA[Other Gladstone]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.engineeringjobs.net.au/jobs.nsf/v/1EE6482579E90083329E</url>
<company><![CDATA[Queensland Alumina]]></company>
<description><![CDATA[Come and join the QAL team! QAL is one of the worlds largest alumina refineries and is an integral part of the coastal community of Gladstone in Central Queensland. Conveniently located only a half days drive north of Brisbane, Gladstone is a gateway to the Southern Great Barrier Reef and Capricorn-Bunker group of islands. It is just over an hour north of the townships of Agnes Water / 1770, a quiet holiday destination known for its relaxed life style and excellent surf. Gladstone is home to a diverse range of industrial sites however, the city is a popular destination for tourists and those seeking an alternative to city living while still offering a range of restaurants, shopping and other facilities. Offering a large range of benefits, QAL employees receive an attractive salary, subsidised health insurance, participation in the QAL bonus scheme, generous superannuation company contributions, free membership to the Yaralla Corporate Lifestyle Package (includes access to gym, movies, golf etc), and much more. We are currently seeking a Lead Electrical Maintenance Engineer to join the QAL team to lead our Electrical Instrumentation Technical Support group within the Engineering and Maintenance Department.    The QAL plant occupies 80 hectares of a 3,050 hectare site and includes a vast range of industrial equipment, instrumentation and technologies including extensive use of Smart MCCs, PLCs and multiple types of Variable Speed Drives. * QAL is one of the largest power consumers in Queensland with a maximum demand of approximately 100MWs supplied from the Powerlink grid by four main 132kV Feeders. * QAL has two 13MW steam powered generators, 9 x 1.25MW Diesel Generators and is currently investigating the feasibility of installing a Cogeneration unit. * Distribution to the 44 main substations is at 11kV via 95 11kV outdoor switchboards and 13 indoor 11kV switchboards. * Site equipment is supplied from the 217 distribution transformers which reduce the voltage to 3300 and 415volts. There are 27 x 3300 volt switchboards and 58 x 415 volt switchboards. * Monitoring and control is facilitated by the integration of thousands of instruments into a Bailey Distributed control system.  Role responsibilities:  * As the Lead Electrical Maintenance Engineer you will be responsible for keeping the site Electrical and Instrument Infrastructure running at its optimum efficiency  * You will be working with the Electrical Instrument Maintenance Team of 124 permanent employees (including engineers, supervisors, tradespersons and apprentices)  * You will be required to provide specialist electrical technical assistance to the Operations and Maintenance departments  * You will lead improvement activities related to equipment safety, performance, reliability and maintenance  * You will also be supported by a group of 8 Electrical/Instrument Engineers in the Engineering Department and a project delivery group dedicated to implementing up to and20M budget for annual capital and maintenance projects  Skills required:  * Electrical Instrumentation trade background (preferred)  * A tertiary qualification in electrical engineering (Bachelor of Technology or higher). In addition, qualifications in Maintenance Systems, experience with an Electrical trade background and a Qld Electrical licence are preferred  * Registered Professional Engineer QLD (RPEQ) or eligibility to attain RPEQ  * Extensive experience dealing with technical issues in an industrial process environment  * Proven experience in people management * Excellent verbal and written communication skills, analytical problem solving and trouble shooting  To apply for this job go to: http://qal.currentjobs.com.au and enter ref code: 907307. Applications close 25 May 2012 ]]></description>
<salary></salary>
<education></education> 
<jobtype>Permanent</jobtype>
<category>Manufacturing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lineworker Leading Hand]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5B024F0ED71E0AC4482579EA00309EB7</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Lineworker-Leading-Hand_1609080.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[Leading Hand LineworkerNegotiable SalarySydney RegionThis key ASP Level 3 electrical contractor is seeing substantial growth throughout their business due to the current NSW CAPEX upgrade projects. Due to their continued expansion they are looking for a experienced Lineworker Leading Hand to join their team  As the successful candidate, you will have previous experience supervising site staff and sub contractors within the Electrical industry you will hold a Certificate III in ESI (distribution) or have an Electrical trade with the relevant Electricity Distribution experience, current Ausgrid and Endeavour authorisation cards, EWP and dogging certificates are required as is a current driverandlsquo;s license.   In return the organisation will offer you a fantastic rate of pay, with plenty of overtime if sought, within a stable andamp; growing company.  To apply, please send your resume to clare.keen@hays.com.au before contacting Clare Keen on 02 9249 2299 quoting 1203487.  Reference Number: 103-1203487]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Merchandise Planner]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob709801DF3DB2C2B4482579EA005521C0</referencenumber>
<City><![CDATA[Sydney CBD]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Merchandise-Planner_1609556.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[ Join a leading retail group as a senior member of the planning team. Due to continued growth and restructure we are seeking experience senior planners and planners for permanent and contract roles. Candidates seeking a six or 12 month contract are encouraged to apply. Candidates with a working holiday visa are welcome to apply.On an interim or perm basis you will be supporting the buying teams in either soft or hardgoods.This role is responsible for ensuring effective analysis of merchandise to ensure profitability and excellent servicing of stores and operates at a senior level reporting in to the Merchandise Manager. Subsequently we are seeking candidates with a minimum of 4 years experience at planner level and ideally currently operating in a volume business or at senior planner level.Employer sponsorship will be given to suitable candidates. Hays Globalink is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the TandCs, Privacy Policy and Disclaimers which can be found at hays.co.uk]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>HR and Recruitment</category>
<experience>3 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Health, Safety And Environmental Advisor]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDB178528F03B29E3482579EB00174D97</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Health-Safety-And-Environmental-Advisor_1609194.html</url>
<company><![CDATA[Morgan McKinley Group]]></company>
<description><![CDATA[ This client has over 800 employees based nationally working on high profile projects, with a large volume of projects spread across NSW they are seeking an experienced HSE Advisor to work across Sydney on numerous projects in Civil construction.  This position will suit an independent, confident HSE Advisor who wishes to take the next step in their career and has the ability to manage projects.Duties will include liaising daily with Project Managers, Construction Managers and crews across each site ensuring regulations are adhered to across health, safety and environmental.  You will manage all documentation, audits and quality inspections for designated sites liaising with contractors and clients daily.  This is a key role within the organisation and requires an individual who is passionate about their role and spreads their enthusiasm and processes across each site.  You will be accountable for site investigations and ensuring each employee is trained and inducted onsite.The ideal candidate will have over 4 years experience in a similar role, ideally with 2 year experience in Australia in the civil construction industry.   Tertiary qualification in Health and Safety along with a qualification in OHS is essential.  Exceptional communication and interpersonal skills are required to achieve best results.For more information on this role please contact Eleanor Barry @ Morgan McKinley 02 8986 3102 or Apply today. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Bilingual Buyer #7737]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 23 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1BB858A04B7B431A482579EB00174D99</referencenumber>
<City><![CDATA[Calgary Region]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Bilingual-Buyer-SHARP7737_1613907.html</url>
<company><![CDATA[Swift Technical Group]]></company>
<description><![CDATA[  Bilingual Buyer   Swift Worldwide Resources is currently recruiting for an intermediate/Senior Bilingual buyer (French/English) for our clients on-site operation in Calgary. This is a permanent position within one of the most recognized and well known Oil sands operator.    Anticipated start date - As soon as possible.    JOB OVERVIEW Based out of our Calgary office, the intermediate/Senior Bilingual Buyer is part of a dynamic team responsible for the procurement of services, sourcing materials and issuing purchase orders.  Reporting to the Procurement Manager, overall responsibilities for this role include minimizing commercial risk, enhancing competitive advantage, meeting clients expectations and specifications.  French bilingualism/fluent proficiency is a requirement for this position (please indicate clearly on the resume).  KEY ACCOUNTABILITIES *Identify and address issues related to the Procurement process, escalating unresolved issues to the Buyer Group Lead.  *Review purchasing requirements for materials and services, obtaining additional information as required.  *Assess and recommend procurement options based on business unit requirements, identifying potential suppliers.  *Conduct negotiations with selected suppliers to tactically procure materials and services.  *Utilizing contracts created by Category Management, accountable to procure materials and services as required.  *Develop short form contracts for the procurement of materials and services. * Create and change purchase orders.  *Respond to supplier and business partner inquiries.  *Work with Supplier, Supply Chain Management and Transportation Analyst to expedite orders as required.  *Assist in resolution of incomplete or incorrect shipments with the supplier.  *Resolve invoice and/or payment issues related to purchase orders.  *Liaise with internal stakeholders to identify improvements to the existing Procurement practices REQUIRED QUALIFICATIONS Our client is committed to employment equity and encourages applications from all qualified individuals Education and Experience: *Experience in the Oil and Gas industry is an asset.  *Experience in supplier analysis, screening and selection.  *A business or Supply Chain Management degree from a recognized institution.  *A minimum of 5 years Supply Chain Management experience.  Skills and Knowledge: *Demonstrated experience and knowledge of tactical procurement process.  *Fluent in French is a requirement.  *Working knowledge of SAP.  *Demonstrated experience in negotiating and executing contractual terms and conditions.  *Effective interpersonal, negotiation, facilitation and communication (both written and oral) skills.  *Ability to deal with competing priorities and manage time appropriately.  *Self starter and the ability to work both in a team environment and independently.  *Proficiency in MS Office and knowledge of materials management software/databases. Our client is committed to employment equity and encourages applications from all qualified individuals.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Sonographer]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 23 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6DDC3256D73C0C9C482579EB004FD8E0</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Sonographer_1614526.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[ An excellent opportunity has arisen for a qualified Sonographer. If you have been thinking of relocating to booming Western Australia, now is your opportunity. With seven sites in the Perth area and an eighth due to open, this is a chance to join an expanding organisation. With additional sites across Australia this role offers potential for further developments in the future. With duties that involve more than scanning, the role is constantly varied and interesting. The organisation is well resourced with state of the art equipment and a well maintained environment. This is a full time, permanent position, where the successful candidate will be required to go between a number of locations all of which are easy access from the CBD.DMU qualifications will be of an advantage and excellent interpersonal skills, a demonstrated ability to communicate effectively with patients, staff members and other stakeholders both verbally and written are essential for this role. 457 Employer Sponsorship will be given to suitable candidates. Hays Globalink is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the TandCs, Privacy Policy and Disclaimers which can be found at hays.co.uk]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>HR and Recruitment</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Clinician]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 23 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2B1EEDE2F5A1D4E0482579EB004FD914</referencenumber>
<City><![CDATA[Victoria]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Clinician_1614529.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[ We are currently seeking Clinicians to provide comprehensive support to our client within the corrections sector. Reporting into the Senior Clinician, you will undertake assessments and successfully deliver a range of relevant services including group intervention. You will be responsible for the delivery and evaluation of programs and maintenance of appropriate records in addition to having an involvement with clinical supervision. You will be a pivotal team member and contribute towards the goal of reducing reoffending rates. To be considered for this role you will need to be registered, or eligible to register as a Psychologist or Social Worker with the Psychology Board of Australia or Australian Association of Social Work. You will have extensive post-qualified experience in similar positions and a demonstrated knowledge and understanding of the Criminal Justice System as well as solid knowledge of Cognitive Behavioural Therapy.The role requires travel between sites across Victoria so therefore you will need to hold a valid drivers license. In return you will be given a competitive remuneration package, excellent career development prospects and an unprecedented opportunity to make a positive impact on others lives. Employers sponsorship is on offer for suitable candidates. Hays Globalink is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the TandCs, Privacy Policy and Disclaimers which can be found at hays.co.uk]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>HR and Recruitment</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[HVAC Estimator]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 23 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB1B4AB093D212BC4482579EB004FD94C</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/HVAC-Estimator_1614535.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[ One of Queenslands top Mechanical Contractors is seeking an experienced Mechanical estimator as a result of expansion. The company are growing and can offer excellent career progression, they are small enough to encourage a great team working environment but large enough to be involved in some of Australias major construction projects, They deal with a range of projects including hospitals, retail, commercial and high spec residential ranging from and1m to and10m+.In order to be successful you will have a proven track record in estimating for Mechanical Building Services Projects for Heating, ventilation and air conditioning (HVAC) Ideally your experience will be gained working for a mechanical contractor or specialist subcontractor.This is an ideal opportunity to be involved in a company with an excellent local reputation and who pride themselves on repeat business by offering bespoke services for their customers, excellent service delivery and maintenance. Hays Globalink is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the TandCs, Privacy Policy and Disclaimers which can be found at hays.co.uk]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Civil Engineer (Construction/Mining Infrastructure) - Liberia]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 25 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob58FDAA1EEDF1BB3A482579EB004C427E</referencenumber>
<City></City>
<Country><![CDATA[LIBERIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.expatengineer.net/job/Civil-Engineer--Construction-Mining-Infrastructure----Liberia-BB3A48.html</url>
<company><![CDATA[CA Global]]></company>
<description><![CDATA[CA Global: Engineering and Construction (Mining Projects) has a client, a world renowned  firm with projects all over the globe, focused on developing and operating mines, building all the mine related infrastructure themselves, looking for a Civil/Construction Engineer with wide experience in the construction of mining infrastructure, ranging from roads, tailing dams, pipelines, concentrator plants etc. If you have the above experience and fit the below requirements then please send me your CV for this role in Liberia.  DUTIES AND RESPONSIBLITIES Ensure that projects are executed in accordance with approved plans and specifications. Monitor project progress to ensure time and budget constraints as well as quality standards are adhered too.  Supervise labour on site. Ensure that HSE and QA/QC standards are upheld on site.  REQUIREMENTS  Must possess a BSc in Engineering at the very least. Non  Negotiable Registration with an  10 - 15 years professional experience in in mining infrastructure construction. Experience having led a construction team on similar projects Risk identifying skills. Strong problem solving skills.  From the client, for the right candidate, you will receive a competitive expat salary package, complete with accommodation, transport, meals and medical insurance. This is a rotational position and is available on single status. Having worked for this company and on such a large project, will add great value to your experience.   If you meet these requirements and you feel that you are suitable for this position, then please send through a copy of your updated CV to Stephen Oakes: stephen@caglobalint.com  If you do not hear anything within 2 weeks after you have submitted your application, consider it to be unsuccessful.  For more job opportunities please visit our website: www.caglobalint.com  ]]></description>
<salary></salary>
<education></education> 
<jobtype>Permanent</jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quantity Surveyor – Major Projects]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 26 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE90E4FDCCB1E9E63482579EB005BE242</referencenumber>
<City></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Alberta Calgary]]></State>
<url>http://www.engineerjob.us/jobs.nsf/v/9E63482579EB005BE242</url>
<company><![CDATA[Canadian Natural Resources]]></company>
<description><![CDATA[THE OPPORTUNITY: Our Horizon Oil Sands operation is expanding with project spending for 2012 forecasted at approximately and2 Billion with similar spending projected each year for the next 5 years.  The Quantity Surveyor is an integral part of growth strategy and you will have the opportunity to:  Verify and Record all quantities completed in the field for each type of contract (lump sum, unit price and cost reimbursable) for the entire team    Assist in Bid Evaluations and Final Account Cost calculations on Contracts as required  Produce takeoffs, measure, and check installed quantities to high standards in a timely manner for:     o Progress Measurement      o Variations and Changes      o Statistics      o Taxation     o Valuation  HOW WILL YOU MAKE YOUR MARK? Maximize your industrial quantity surveyor experience within oil and gas coupled with your analytical and interpersonal skills to:   Review estimates to an appropriate level of detail to support the review of contractor claims and change order requests. Ensuring all contractor work is in accordance with CNRL Standards and Procedures  Review and verify total installed quantities for all disciplines including civil, structural, mechanical, piping, electrical, and instrumentation through regular review of contractor work  Collect and assemble benchmarking data  Validation of installed items for Unit Rate contract progress payments  Assist Contract Administrators in measurements for bills of quantities and also assist in tender or bid evaluations  Apply your skills to project opportunities in the following areas:  Extraction Plant  Froth Treatment Plant  Tailings Transfer Treatment Plant  Ore Preparation /Hydrotransport Plants   Coker Expansion Projects  QUALIFICATIONS:   Typically 5+ years of related industry experience with Quantity Surveyor Diploma or relevant degree and exposure to estimating software   HEALTH AND SAFETY: At Canadian Natural, safety is a core value.  We conduct all of our operations in a way that identifies, minimizes and mitigates harm to the health and safety of employees, contractors, the public and the environment.  Only those candidates selected for an interview will be contacted.    ]]></description>
<salary></salary>
<education>HND/Diploma</education>
<jobtype>Not Specified</jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[Clinical Care Coordinator RN]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEC64816E597F9E69482579EC001166C0</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Clinical-Care-Coordinator-RN_1618340.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Friendly team, lovely environment, work / life balance Generous Salary packaging Exciting career step with ongoing training Fantastic opportunity for an experienced RN to move into a Coordinators role, positively leading the care team and working closely with a supportive Care Manager.  The role:   Coordinate provision of care to permanent residents and for a day respite program, focussing on quality service, continuous improvement and people developmentProvide quality services and the highest level of care to meet the needs of the residentsDevelop the care framework and team in collaboration with a supportive Care ManagerPositively lead the staff and carry out appraisals Does this describe you? An Aged Care Manager or an RN looking to take that next stepRegistration with APHRAExperience in the accreditation process and gaining ACFI funding will be highly regarded but not essentialAn enthusiastic and energetic RN dedicated to the delivery of high standards of resident care Benefits: Generous salary packaging arrangementsWork/life balanceSupportive manager - scope for innovation and autonomy    To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Rhys Kane on 0424149273, quoting Ref No. JIDN5015.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Hospitals Health and Medical</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Document Controller]]></title>
<date>Wed, 25 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 23 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8F5C180C2CD7EC62482579EC0016C4AD</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[SCOTLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Senior-Document-Controller_1614444.html</url>
<company><![CDATA[INTEC (UK) Ltd]]></company>
<description><![CDATA[Role: Senior Document Controller Location: Aberdeen Type: Contract Duration: Long term Rate: Negotiable  Job purpose: Required to assist in managing the daily performance and operation of Document Management Centre on ongoing project. This includes all DM activities required to meet the needs of the onshore and offshore operations within both the clients organisation and the Client.   Role and Responsibilities: - To process both design and vendor documents in accordance with corporate or project procedures  - To process all documentation received in DM in accordance with prescribed matrices within agreed timescales. - To allocate and control the numbering of documents and drawings produced on the project - To accurately update information in both Client and the Clients electronic document management systems - To perform supervisory duties, resolve procedural issues, assign work to more junior staff (as applicable) to achieve targets/milestones - To assist in completing requests, searches and queries for any project personnel. - Liaise with engineers, clients, suppliers or third party companies as required to complete DM function on project  Knowledge, Skills and Experience: - Educated to Standard Grade level (pref to include Technical/Engineering, English, Science, Maths) - Information Management or Librarian or Computer qualifications (desirable) - Experienced in working in an engineering project group or document management centre - Capable of processing both Design and Vendor project documents - Experienced in use of electronic document management systems - Good understanding of working to procedures and project deadlines - Supervisory skills - Good understanding of electronic file production/formats  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>1 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Estimating Manager  Commerical Construction]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9BFE8DBA79EF7F62482579EC001CC57D</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Estimating-Manager-Commerical-Construction_1618369.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a West Australian Developer and Builder that has been creating highly successful property developments, land subdivision and construction projects for many years. They have a Group of Companies that, with combined capabilities, provide an unparalleled resource for property development.  Due to a substantial Company restructure, our client is currently seeking an experienced Estimating manager to assist in driving the Company in the right direction and maintaining a high level of service to the Building and Construction industry.  We are looking for someone with experience in Estimating within the Building environment, who is familiar with risks related to the building industry and who has experience with residential and building projects.  Reporting to the CEO, the responsibilities of the Estimating manager will include (but is not limited to); Tender Management Manage a team of Estimators across a Group of CompaniesInterfacing with the front end of the business including Engineering and ProcurementReview specification and drawings to complete bid review formsPerform bid evaluationsPrepare concept layouts for estimating take offsReviewing all estimates prior to submissionProvide pricing in a timely mannerFollow up tender results and update tender registerDevelop and maintain client relationships We are looking for a candidate who has a high level of initiative and andlsquo;get up and goandrsquo;. You must be an excellent communicator and Australian experience is essential.  You will be rewarded with a long term career, a competitive remuneration and potential career advancement as the company continues to grow.       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pipe Stress Engineer  Mechanical & Piping Engineer   Onshore Oil and Gas]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF2FE1337755FACE4482579EC002F5451</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Pipe-Stress-Engineer-Mechanical-and-amp-Piping-Engineer-Onshore-Oil-and-Gas_1618625.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.     Due to ongoing work and an increase in demand, they are now seeking an experienced Mechanical andamp; Piping Engineer with Pipe Stress Engineering experience to join their team in Perth CBD. We are looking for candidates who have experience working on onshore gas plants in Australia.     We are seeking Mechanical Engineers who have a high level of experience in the oil and gas industry and the successful candidate will ideally have the following experience: Piping stress analysis experience in a Consulting / Engineering environment pertaining to Hydrocarbon / Petro-chemical / Oil andamp; Gas sectors.In-depth knowledge in stress analysis and using Caesar IIAdequate knowledge in Piping layout, Design of Supports, Hanger selection etc.Knowledge of dynamic analysis will be considered an added advantage. In order to be successful, candidates will also be required to experience on:    Plot Plans, Piping Layouts,Piping Specifications, Valve specificationsStress AnalysisVendor quote evaluationsVendor quote evaluationsVendor drawing review and approval    In order to be successful, candidates will be required to; Mechanical Engineering DegreeMinimum of 5 years in a similar roleCommercial awareness for project evaluation and submission for approvalClear and respectful communication skills at all levelsHighly developed time and task managementGood understanding of Australian codes and standards    The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the downstream oil and gas industry.     If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal & Lead Process Engineers  Mining & Minerals]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob38DFE5E524DADF8D482579EC002F5478</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[South Australia]]></State>
<url>http://www.expatengineer.net/job/Principal-and-amp-Lead-Process-Engineers-Mining-and-amp-Minerals_1618626.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking to engage a Principal and Lead Process Engineers , to become part of the team that coordinates the technical development and assist the commercial team in the development of Greenfield and Brownfield projects through pre-feasibility / feasibility studies. This is a permanent, full time role in Adelaide.     Our client is seeking personnel at various levels of their engineering degrees.     The Person  The successful candidate will ideally have the following qualifications and experience:     Bachelor of Engineering A minimum of 10 years experience as a Process Engineer Mining andamp; Hydrocarbons industry experience Pre-feasibility/Feasibility study work.     Your responsibilities may also include, but will not be limited to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts; andFor the more senior candidates; a provision of technical guidance to junior engineers and peers.       We are looking for candidates who have a well developed understanding of the Mining and Mineral Processing industry.  If this sounds like you then please apply now!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Assistant  Engineering]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAE7ABBE930344BA9482579EC002F5496</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Technical-Assistant-Engineering_1618627.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Assistant to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsHelp with proposalsAssist with invoicingAssist with writing technical dcuments and manualsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleA relevant qualification would be advantageousExcellent MS office skillsTechnical/Electrical drafting backgroundGood organisational and administrative skillsBe a team playerEnjoy a busy work environment If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Control Systems Engineer  Mining & Resources]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob914A7A21AA6E36F1482579EC002F54B8</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Lead-Control-Systems-Engineer-Mining-and-amp-Resources_1618628.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in West Perth. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer.  The role of the Lead Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 5 years industry experience in the Australian market Candidates will be required to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Provision of technical guidance to junior engineers and peers;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts.    The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activities    We will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Mechanical Engineer  Oil & Gas  Hydrocarbon]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB019B3337EC30FFB482579EC002F54D6</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[VICTORIA]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Mechanical-Engineer-Oil-and-amp-Gas-Hydrocarbon_1618629.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking highly experienced Mechanical Engineers who have experience in the Oil andamp; Gas and Hydrocarbon industries, to join the growing team in Melbourne.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and Gas / Hydrocarbon IndustriesDegree or equivalent experience/qualificationsExperience in Engineering from FEED, Detail to Project DeliveryTechnical writing and design specification experience Australian experience    The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.       We are looking for candidates who are able to display at least 5 years experience in Mechanical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Control Systems Engineer  Mining in Mackay]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7297F966668AE2C8482579EC002F54F3</referencenumber>
<City><![CDATA[Mackay]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Control-Systems-Engineer-Mining-in-Mackay_1618630.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in Mackay. The ideal candidate for this role will be someone who has a reliable level of experience in design and project management within the mining and resource industry. You should now be at a level where your management skills are well developed, or you are now ready to expand into this responsibility.     The role of the Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.  The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportExpereince working in Regional Areas5 years industry experience in the Australian market The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; OIS programming and testingElectrical engineering including designProject management activities    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Electrical Designer  Engineering]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob342806C51ADB5991482579EC002F5510</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Lead-Electrical-Designer-Engineering_1618631.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking an experienced Lead Electrical Designers to join the Brisbane team. Drafting diploma or equivalent, specialising in ElectricalAdvanced knowledge of Australian Design Codes and Standards. Intermediate knowledge of MS Excel and Word. 15+ yearsandrsquo; experience in Electrical design drafting within an industrial environment. Brownfield/Greenfield Project Experience.Mining/Hydrocarbons experience EssentialProven experience in similar role    The company is actively expanding and is seeking applicants for the role of Lead Electrical Designer based in the Brisbane office. Full time, contract or casual employment arrangements will be considered for this role. Donandrsquo;t miss this excellent opportunity, please send your application through now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Officer  Electrical drafting]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCB29964A02C06491482579EC002F552F</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.expatengineer.net/job/Technical-Officer-Electrical-drafting_1618632.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Officer, with an electrical background to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsAssist engineers with design of HV/LV plant.Assist in the development of technical documents, specifications and manualsHelp with proposalsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleDiploma in Engineering or Electrical Licence is desirable.Experience in power distribution and drives (LV/HV).Development and review of electrical design deliverables (SLDandrsquo;s / schematics / GAandrsquo;s / schedules).Exposure to an industrial engineering environment or office.Exposure to electrical drafting.Experience in electrical design and drawings. If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Draftsperson Mining Operations]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA953D6F454F334A1482579EC002F5588</referencenumber>
<City><![CDATA[West Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Draftsperson-Mining-Operations_1618634.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.  As part of ongoing expansion, the Perth team is looking for an Electrical Draftsperson to join the team and work across multiple materials handling projects for the resource sector. This role offers some opportunity for growth within the company so your skills can be practically developed working with larger teams of engineers and technicians.     The ideal Drafter will have had experience using electrical Autocad and have experience with; Drawing up electrical single line diagramsElectrical schematicsPanel arrangements and associated termination and cable schedulesLoop diagrams We are looking for candidates who have around 5+ years experience in a Drafting role and are interested in developing their career in the Mining industry.  The successful candidate will need to be: Be a self-starter who thrives on taking ownership of their role and has the ability to work with minimal supervision;High level of integrity and a proactive approach in all job related activities; Well developed written and oral skills. Offered is a: Competitive salary package; Career growth and development opportunities. If this sounds of interest to you than please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Project Engineer  Onshore Oil and Gas]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob328B84DB2C21BAC1482579EC002F55AB</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Electrical-Project-Engineer-Onshore-Oil-and-Gas_1618635.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our Client is an outcome focused project management service provider specialising in project feasibility, management and completion services to the midsized Gas and Energy sector.   Reporting to the General Manager, the primary responsibility of the Electrical Project Engineer will be to administer, manage and control all aspects of the project, including all interface services. You will be responsible for ensuring that the various stages of the project are safely completed by the scheduled dates within the allocated budget and to the specific standard of workmanship and quality.   In order to be successful candidates will be able to demonstrate; A Bachelor or Diploma degree in Electrical Engineering;5 years experienceA background in oil andamp; gas construction;A well developed commercial acumen;Experience in the management of tendering issues, design, procurement and construction;A commitment to safety, quality and teamwork;Project Engineering experience in the Australian environmentBe willing to do some site work as required  Successful candidates will need to be outcome focused, motivated and willing to take on multi discipline challenges for project delivery If you can demonstrate your knowledge and experience in the above requirements and in particular a strong familiarity with the Australian market, we would welcome your application. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Underground Mining  Senior Project Manager]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5F8327DC28EB3404482579EC002F55D7</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Underground-Mining-Senior-Project-Manager_1618636.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ The Company  Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     The Role  They are currently seeking an experienced Project Manager required to manage operations in WAs norhtwest. The ideal candidate will have a well developed understanding of Underground Mining operations and have be able to demonstrate a high level of experience in Project Management, preferably with Contractor organistions. Reporting to the Operations Manager, the Project Managerandrsquo;s role will include acting as the overall Site Manager; ensuring consistent standards are met and be the main point of contact for the client.        The Requirements  As the successful candidate, it is essential that you possess the following skills and experience: Tertiary Qualifications Mining Engineering or Management or related areaConsiderable experience in mine management, shotcreting and shaft lining and managing large mulit million dollar projectsPrevious leadership experience over a variety of departments including project control, commercial, ops readiness, HSE, and engineering.A passion for achievement through team building and culture A demonstrated focus and commitment to commercial imperatives and the time critical elements of successful mine operations.       The Rewards  The position offers a competitive remuneration of up to and200,000 to and220,000 base salary pa and the work is challenging. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical or Structural Drafter  Mining]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob60DE3A473A34B327482579EC002F55F1</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mechanical-or-Structural-Drafter-Mining_1618637.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     As part of ongoing expansion, the Perth team is looking for a Draftsperson to join the team and work across multiple materials handling projects for the resource sector. This role offers some opportunity for growth within the company so your skills can be practically developed working with larger teams of engineers and technicians.  The ideal Drafter will come from an Mechanical or Structural background, have experience using INVENTOR and have had some experience in the resource industry, preferably Mining.        We are looking for candidates who have around 3+ years experience in a Drafting role and are interested in developing their career in the Mining industry.  The successful candidate will need to be: Be a self-starter who thrives on taking ownership of their role and has the ability to work with minimal supervision;High level of integrity and a proactive approach in all job related activities;Well developed written and oral skills. Offered is a: Permanent full-time position andndash; Airport location;Competitive salary package;Career growth and development opportunities.    If this sounds of interest to you than please apply now!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining & Materials Handling Mechanical Design Engineer]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob12AE2836F73DBC60482579EC002F560E</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-and-amp-Materials-Handling-Mechanical-Design-Engineer_1618638.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.        They are currently seeking a Mechanical Design Engineer who has had experience working on Mining and Infrastructure or Materials Handling related projects, to join the team based near the Perth International Airport.     The ideal candidate will need to demonstrate: Experience in mechanical design and project management in the mining industryKnowledge and good understanding of materials handling projects    In order to be successful, candidates will be required to display; Bachelor of Mechanical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety;    The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining & Materials Handling Mechanical Design Engineer]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob61156E0D849216C8482579EC002F562C</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-and-amp-Materials-Handling-Mechanical-Design-Engineer_1618639.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.        They are currently seeking a Mechanical Design Engineer who has had experience working on Mining and Infrastructure or Materials Handling related projects, to join the team based near the Perth International Airport.     The ideal candidate will need to demonstrate: Experience in mechanical design and project management in the mining industryKnowledge and good understanding of materials handling projects    In order to be successful, candidates will be required to display; Bachelor of Mechanical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety;    The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Estimator  Mining Services]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8C0F6A78042CB753482579EC002F564B</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Estimator-Mining-Services_1618640.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     As part of ongoing expansion, a position has become available for a qualified and experienced Electrical Estimator to join their team located near Perth International Airport.     The ideal candidate will be required to provide accurate estimates of the total cost of allocated projects. Experience estimating in the electrical discipline within the construction and/or industrial sector will be highly regarded.     The Key Duties will include however not be limited to: Production of realistic but economical project cost estimates for the preparation of major feasibility studies and tenders Preparation of bids, selection of vendors or subcontractors, and determining cost effectiveness Conducting special studies to develop and establish standard hour and related cost data or effect cost reductions. Maintenance of the electrical cost databaseParticipating in regular estimate reviews Preparing presentation/reporting formats for cost/estimate information as required     You will need to be able to work autonomously as well as collectively as a team to meet project goals, have an enthusiastic and proactive approach and take pride in the quality of your work.     Previous estimating experience at a senior level with a thorough knowledge of engineering and construction processes in the mining/resource development of minerals processing industry is essential.  The Successful Applicant will also need to meet the following criteria: Good overall computer skills including Word and Excel, and the ability to pick up new systems quicklyOrganisational, time management and communication skills. A high degree of professionalism with customers; strong communication and interpersonal skills Be capable of measuring electrical documentation and producing bill of quantities; Be customer-focused and demonstrate proficient communication and business writing skills; Be capable of identifying and valuing variations; and Be prepared to price or assist in the valuation of variations and financial claims.  If this role sounds like your next job than apply now!!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining Engineer  Underground Operations]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9D76A2D3B066892482579EC002F566C</referencenumber>
<City><![CDATA[West Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-Engineer-Underground-Operations_1618641.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking a Mining Engineer who will be responsible for the effective application of mine planning processes, verification of contractual activity, assess the effectiveness of mining performance, reviewing cost performance of mining operations.     The responsibilities of the Project Mining Engineer will include (but are not limited to); Develop and implement mine planning systemsDevelop and implement short term mine scheduling to support operational performance.Prepare the data required for day works claims and monthly claims.Maintain client relationships, offering technical solutions to site and client issues.Support efficient mine planning and contractual claims.Manage the efficient supply of external products and services to support the operation.Provide a technical contribution to initiatives and other projects . In order to be successful, candidates will be required to display; Bachelor of Mining Engineering;Minimum 3 years experienceGood interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities; andA commitment to safety. Candidates who have had experience underground will be highly regarded. Previous experience in a Contractor environment will also be advantageous.        The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Site Supervisor]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 24 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob179CF597811B415D482579EC0037B70A</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Site-Supervisor_1618375.html</url>
<company><![CDATA[Morgan McKinley Group]]></company>
<description><![CDATA[ My client is a leading civil infrastructure business and currently seeking a Site Supervisor to work on various projects across the Gas industry.  With a strong reputation for delivering projects on time and within budget they require a confident site manager to assist the project manager with planning and managing site crews to ensure all key areas of the site are working to full potential.  This position will suit an experienced site supervisor or ambitious team leader seeking career development. Extensive experience in the Gas industry essential.You will liaise daily with the management and Civils team to ensure projects are completed to cost, time, quality and performance.  You will delegate tasks daily to crews and ensure activity reports are compiled while holding toolbox meetings to ensure consistency and team work throughout the projects.  You will be accountable for HSEQ standards and regulations ensuring they are adhered to and promote a zero tolerance culture across this area.The successful candidate will be trade qualified with extensive industry experience across civil construction.  You will have over 3 years experience in a leadership role within the Gas industry.  Excellent communication and interpersonal skills are required along with proven experience enhancing team work initiatives.For more information on this role please contact Eleanor Barry @ Morgan McKinley on 02 8986 3102 or apply today!      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>3 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Regional Operations Manager  Underground Mining]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob84D0E8CA759C3AEE482579EC00438144</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Regional-Operations-Manager-Underground-Mining_1618819.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking an Operations Manager with experience in the Underground Mining industry. Based either at the head office in Brisbane or Perth, you will be required manage and oversee the underground mining operations on the East Coast.     Reporting to the General Manager of Underground, your primary responsibility will be to oversee the satisfactory performance of various core function support and service areas and to oversee the safety, quality, schedule and budget performance of the underground projects group.  Your responsibilities will include; Providing operational support to the Project TeamsReviewing all Financial and Progress reportsReviewing scopes of workLiaise with all internal and external stakeholders to ensure strong relationships with the team and with the clientEnsure that all Project Management Plans are followedEnsure that Contract Conditions are met to the clients satisfactionReport to the Corporate Management Team quarterly analysis on performanceProduce and manage action plans for the divisionLiaise with immediate Administration teamBuild company profileEnsure tenders are evaluated and responded to in a timely and professional manner    Your experience within the Underground Mining Industry will be highly regarded and candidates will be required to have a Mining andamp; Engineering background.  A minimum of 10 years industry experience is required.  There will a number of direct reports so it is essential that you have good people skills, an effective management style and excellent communication abilities. A well-developed commercial acumen is also very important.  The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CivilStructural Engineering Manager]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob35BA4E238DD07BE3482579EC0043817D</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Civil-Structural-Engineering-Manager_1618820.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons and other industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations.  They are currently seeking an experienced Manager who can head the Civil / Structural division within the business, as well as provide technical assistance to the team and engage in business development activities. Preferred candidates will be experienced in the full range of feasibility studies, detailed design and construction.  The responsibilities of the Civil / Structural Manager include, but not be limited to: Manage a Civil / Structural Engineering team in the preparation of feasibility studies, preliminary and detailed designs, and construction.Ensuring all Civil andamp; Structural engineering work complies with statutory and regulatory requirements and company policies and practices.Providing high level technical support for all Civil and Structural engineering work as required.Supervising preparation of documentation for standards, procedures, safe working practices and monitoring regimes in respect of work on or around electrical and instrumentation equipment.Oversee, mentor and develop junior and intermediate Civil and Structural engineers.Perform regular competency assessments of staff team members, develop training and development plans. In order to be successful, candidates will need to have: Professional Degree in Civil or Structural Engineering.Minimum of 15 years experience in the heavy industry, preferably in the mining and hydrocarbons sector.Well-developed management skills and commercial acumen.Excellent communication skills.Excellent people skillsStrong time-management skillsStrong Business Development skills. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the resource industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Planner(Corporate)]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7EBC8723AB1901C3482579ED000ECE34</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-PlannerCorporate_1623004.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Salary PackageGreat Career ProspectsLarge Scale Projects Senior Project Planner - Corporate Role      Our Client is an innovative contractor specialising in the non process infrastructure for the Resource/LNG industry. Due to vast growth, they are looking for a number staff, including a Senior Project Planner.       The company purely works in the booming resources sector on the LNG and Mining remote projects throughout Australia.  The company has a proven track record for strong relationships with their clients in the industry resulting in return work after each project.     The Project Planner will be based in the companies Perth office. They will have a dedicated background in resource construction. The candidate will be able to lead a team of workers and have good a disciplined manner, as well as consistency on their workload with no issues in what they do. They will show strong initiative and demonstrate loyalty to the projects. The candidate will have minimum of 5 years experience in the industry and have proven senior experience, working on large scale projects.      As a reward, the company will have a competitive salary and provide a solid platform to develop your career.    We know that every employee has something important to say, and that every employee is integral to their success, appreciation is the best motivation.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Planner (FIFO)]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3A5A7C8ADD201997482579ED000ECE6B</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Planner-FIFO_1623005.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsGreat Salary PackageLarge Scale Projects Senior Project Planner - FIFO    Our Client is an innovative contractor specialising in the non process infrastructure for the Resource/LNG industry. Due to vast growth, they are looking for a number staff, including a Senior Project Planner.       The company purely works in the booming resources sector on the LNG and Mining remote projects throughout Australia.  The company has a proven track record for strong relationships with their clients in the industry resulting in return work after each project.     The Project Planner will be on a FIFO roster. They will have a dedicated background in resource construction and will ideally also have remote mining or LNG work experience. The candidate will be able to lead a team of workers and have good a discipline manner, as well as consistency on his workload with no issues in what they do. They will show strong initiative and demonstrate loyalty to the projects. The candidate will have minimum of 5 years experience in the industry and have proven senior experience, working on large scale projects.      As a reward, the company will have a competitive salary and provide a solid platform to develop your career.    We know that every employee has something important to say, and that every employee is integral to their success, appreciation is the best motivation.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Managers]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF16275E8EBD0F9A9482579ED000ECE9C</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Managers_1623006.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProgressionGreat Salary packageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Managers    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Engineer (East Coast)]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1AF2AA061B184E07482579ED000ECEB9</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Engineer-East-Coast_1623007.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectGreat Salary PackageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Engineers.    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Engineer (WEST COAST)]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8248DE23DFECB7EF482579ED000ECEF3</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Engineer-WEST-COAST_1623008.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsGreat Salary PackageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Engineers    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression Of Interest Planners]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB89D6F4C23542F11482579ED000ECF21</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-Of-Interest-Planners_1623009.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsMajor ProjectsGreat Salary PackageACRWORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planners, Planning Engineers, Planning Managers and Project Planners .    ACRWORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.      In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer    Mining Services]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 22 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE07254FD2B0D09BE482579ED0032CBC2</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Engineer-Mining-Services_1622944.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking an Electrical Engineer who has had experience working on Mining and Infrastructure related projects, to join the team at the office located at the International Airport. Ideally, the Electrical Engineer will want to grow and develop with the company as there are many opportunities for career development.    The ideal candidate will have demonstrable experience in:The electrical design relating to underground mining infrastructure, including the equipment such as crushers and conveyors;The supervision of a team of Engineers;A strength in Design with experience in Project Management.At least 4 years + LV Switchboard design and motor control centres experience    In order to be successful, candidates will be required to display; Bachelor of Electrical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety.    Candidates will be required to have minimum of 5 years experience in similar role and previous experience in a Contractor environment will be highly regarded.     To be successful, you will need to have project management and supervision experience, preferably with a contractor.  The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Structural Engineer]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 22 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob29B99EA24A1F5814482579ED0032CBFD</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Structural-Engineer_1623488.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.  Due to ongoing work and an increase in demand, they are now seeking an experienced Senior Structural Engineer to join their team in Perth who are working on an onshore gas plant in Western Australia. The successful candidate will ideally have the following qualifications and experience: Bachelor of Engineering (Civil/Structural)Minimum eight years relevant experienceAn emphasis on structural engineering with exposure to civil engineeringHighly developed technical skills in structural steelConcrete design skillsDemonstrated engineering experience in Oil andamp; Gas / Hydrocarbon industry experience preferredAustralian citizenship or permanent residency essential The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the oil and gas industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer  Electrical  Onshore Oil and Gas]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 22 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD44EDC623C53E577482579ED0032CC1F</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Project-Engineer-Electrical-Onshore-Oil-and-Gas_1623489.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our Client is an outcome focused project management service provider specialising in project feasibility, management and completion services to the midsize Gas and Energy sector. In response to increased project activity we are seeking suitably qualified and energetic Electrical Engineers to join this Oil and Gas Project Services Group and to assist with general project and design management duties.   The successful applicant will ideally possess: Bachelor of Engineering (Electrical)Solid understanding of Hazardous AreaHigh end computer literacyWell developed written and verbal communication skillsSite Commissioning experience will be an advantageProven record in site support5 years industry experience in the Australian market  You will also be required to assist in the control and monitoring of schedules and financial aspects of a project with the team in liaison with the Project Manager.   The successful applicant will have proven technical skills in: Electrical EngineeringElectrical engineering including design and proejct activityDiscussions with various stakeholders (site operational people to extract information)Project Engineering through implementation phases of the projectTechnical / Report Writing  We will be looking for candidates who have experience in Electrical Engineering within the Resource industry and candidates with HA experience will be highly regarded. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then we welcome your application.     ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Exploration Geologist]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2FBAD0CF5922ADD1482579ED003BB1BC</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Exploration-Geologist_1623411.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[Based in Townsville, QueenslandRegional grassroots explorationBase metals and gold discoveryThis ASX listed organisation holds an impressive portfolio of mineral exploration projects across Australia and are seeking an experienced Exploration Geologist to join their team.   You will play a significant part in the continued exploration of early stage grassroots and advanced projects scattered across regional North Queensland.   Responsibilities will include the design of drill plans and target generation, coordinating and supervising DD / RC drill programs, analysis and logging of core and chips, field mapping andamp; modelling and generating accurate reports and documentation.   We are seeking a challenge hungry and degree qualified individual possessing a minimum of 3+ years experience in exploration, solid communication skills and competence in GIS software packages.  Based in Townsville, Queensland and working amongst this close-knit team, you will relish in the hands-on responsibilities and divers challenges this role will offer.   For further information or to apply, contact Bonny Lamont today on: T: (07) 4771 5100 or  E: bonny.lamont@hays.com.au]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mobile Plant Diesel Mechanic  Australia]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA6A118638461D08D482579ED00483CD7</referencenumber>
<City><![CDATA[North Yorkshire]]></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Mobile-Plant-Diesel-Mechanic-Australia_1623693.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Diesel/Plant Fitter - Australia  Acorn is working in Partnership with a leading Industrial and mining services company at Various locations in Australia, we currently have opportunities for Diesel/Plant fitters to work on a fixed term 3 year basis in Australia, with very strong possibility of these roles becoming permanent.   Purpose of Position:  Repair and maintenance of Mobile Plant and equipment, to achieve maximum equipment availability and productive life through preventative maintenance. Ensure that all work and tasks are conducted in a safe manner, and that work practices minimise risk.   Person Specification    Timed served Apprentice is essential   Heavy earthmoving repair and maintenance industrial experience.   Up to date mechanical knowledge with heavy haulage and earthmoving equipment.   Good written and spoken communication skills, and the ability to work at various levels  role   Carry out repairs and maintenance on all mobile equipment and fixed plant, in accordance with manufacturers specifications   Troubleshoot and resolve maintenance problems as they occur.   Support and embrace a preventative maintenance system.   Complete all work orders accurately.   Complete all fleet records so that effective reporting and scheduling may be maintained.   Identify and assist in purchasing parts.   Ensure all work is to a high standard.   Create and maintain a high standard of workshop and yard housekeeping   Able to take directions from Maintenance Manager and representatives.   Work with and communicate with other team members effectively.   Ensure that safety concerns are paramount above production issues and immediately report any near misses, injuries, accidents or non-conformance to the Shift manager.   Carry out tasks in accordance with Policies, Procedures, Work Instructions   Package:  42,000 - 79,000 per annum, full benefits package including, 9% pension contribution, free flights, assistance with accommodation , support to complete visa and transfer from UK to Australia    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Engineer (Drill)  Australia]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA8C2026E504CDA6F482579ED00483D20</referencenumber>
<City><![CDATA[West Yorkshire]]></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Senior-Engineer-Drill-Australia_1623766.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Senior Engineer (Drill) - Australia    Role:   To assist in the supply of technical mining services for use in preparation of mining proposals and tenders     To participate in the review, study and implementation of technical mining activities and systems for the Operating Groups     To assist with project acquisition and development     To provide estimating and tendering services     To assist in developing improvements to the drilling and blasting methods and systems in the operating regions    To ensure that the most competitive drilling and blasting methods are understood and incorporated in mining tenders    Specifically the role is accountable for:     Compliance with all Company policies and procedures    1 Verification of drilling and blasting data used in the preparation of tenders to ensure uniformity and accuracy throughout the company    2 Manage the collection of drilling and blasting data from existing sites for use in the preparation of tenders    3 Assist in the provision of reviews, studies and assistance with mining system implementation when required by operations    4 Participate in major mining and earthmoving tenders when required    Job Specification: (essential or desirable qualities required - ie. education, knowledge / skills)     Tertiary qualifications in either civil / mining / mechanical engineering together with substantial open cut mining and civil construction estimating experience     Computer literacy essential    1 Technical and analytical skills in relation to mining activities and mining equipment    2 Sound interpersonal and team work skills      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Engineer (Blast)  Australia]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob38EFF935343FAF6C482579ED00483D5C</referencenumber>
<City><![CDATA[Derbyshire]]></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Senior-Engineer-Blast-Australia_1623767.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Senior Engineer (Blast) - Australia    Role:   To assist in the supply of technical mining services for use in preparation of mining proposals and tenders     To participate in the review, study and implementation of technical mining activities and systems for the Operating Groups     To assist with project acquisition and development     To provide estimating and tendering services     To assist in developing improvements to the drilling and blasting methods and systems in the operating regions    To ensure that the most competitive drilling and blasting methods are understood and incorporated in mining tenders      Specifically the role is accountable for:     Compliance with all Company policies and procedures    1 Verification of drilling and blasting data used in the preparation of tenders to ensure uniformity and accuracy throughout the company    2 Manage the collection of drilling and blasting data from existing sites for use in the preparation of tenders    3 Review of the relevant technical and operating advances throughout the industry to ensure competitiveness of methods employed in drilling and blasting    4 Assist in the provision of reviews, studies and assistance with mining system implementation when required by operations    5 Participate in major mining and earthmoving tenders when required    Job Specification: (essential or desirable qualities required - ie. education, knowledge / skills)     Tertiary qualifications in either civil / mining / mechanical engineering together with substantial open cut mining and civil construction estimating experience     Computer literacy essential    1 Technical and analytical skills in relation to mining activities and mining equipment    2 Sound interpersonal and team work skills      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining Engineer]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob66EBB1EBB3006BF6482579ED00483DD6</referencenumber>
<City><![CDATA[Chorley]]></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Mining-Engineer_1623770.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Mining Engineer - Australia    Role:   To assist in the supply of mine planning services to site across Western Australia for use in preparation of mining proposals and tenders   To participate in the review, study and implementation of mine planning activities and systems for the Operating Groups   To provide support tendering services   To assist in developing improvements to the mine planning methods and systems   To ensure that the most competitive mine planning methods are understood and incorporated in mining tenders    Specifically the role is accountable for:   Compliance with all Company policies and procedures   Verification of mine planning data used in the preparation of tenders for Xmas creek to ensure uniformity and accuracy   Review of the relevant technical and operating advances throughout the industry to ensure competitiveness of methods employed in mine planning   Manage the provision of mine planning reviews, studies and assistance with mining system implementations when required by Operations   Participate in major mining and earthmoving tenders when required    Job Specification:    Essential Qualities   Tertiary qualifications in either civil or mining engineering together with open cut mining estimating experience   Computer literacy essential   Technical and analytical skills in relation to mining activities and mining equipment   Sound interpersonal and team work skills    Desirable Qualities   Experience with design and operating aspects of metalliferous and coal mines    Package  Salary range from 100,500 to 134,000 plus pension, full relocation package, free transfers from UK to Australia.      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Oil & Gas  Client Manager]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 22 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob56C747033F58AB10482579ED004B8416</referencenumber>
<City><![CDATA[New Plymoth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Taranaki]]></State>
<url>http://www.engineeringjobs.net.au/job/Mechanical-Engineer-Oil-and-amp-Gas-Client-Manager_1623551.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client provides engineering design and implementation solutions for the oil, gas and chemical industries internationally. From concept to operation, they are involved with engineering, design, drafting, and project management.   Due to an increase in workload and oncoming opportunities they are seeking a Client Relations Manager with a Mechanical Engineering background, to be based at their New Zealand offices New Plymouth. This is a long-term position involving Client Management, working with key stakeholders and developing new business opportunities in high pressure gas industry, specifically around onshore pipelines and associated facilities.   Candidates will be required to have a solid understanding of the downstream oil and gas and be recognised in the industry with a track record of engineering and project delivery. The role of the Client Relations Manager / Business Development will include, but not be limited to;   Manage existing clients with the aim of strengthen relations and generating more work;Develop a deep relationship and detailed understanding of each key stakeholder needs and wants;Attend networking, industry and other relevant events to generate new prospects;Complete regular reporting and forecasting as directed;Build strong relationships with prospects;Organise and conduct a proposal presentation;Represent the Company brand , team, products and services in a professional mannerInterfacing with Executive Directors and other business unit managers for coordinated business development activitiesProvide correct technical information to key stakeholdersProvide best engineering and project practicesYou may also be required to undertake chargeable project work to meet agreed limitsIdeally, candidates will have had previous experience as a Mechanical Project Engineer in the oil and gas or EPCM industry and have developed their career into Client Management or Business Development role. You will need to be a Qualified Professional Engineer with at least 10 yearsandrsquo; experience. It is essential that you have excellent communication and negotiation skills, both written and verbal and we are seeking candidates who have good client relationship skills.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Controls Systems Engineer  Mining Sector]]></title>
<date>Fri, 27 Apr 2012 00:00:00 GMT</date>
<Closedate>Fri, 22 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF213A5F70A4531AD482579ED004B843C</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Controls-Systems-Engineer-Mining-Sector_1623552.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   Due to growth and development, they are currently seeking an experienced Control Systems Engineer to join the team at their offices located near the Perth International Airport. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer within the resources sector, in particular mining. The successful applicant will ideally possess: Bachelor of Engineering (Electrical) Experience in Project Management, preferably within the mining sector Experience working on proposals and TendersHigh end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 7 years industry experience Experience working in the Australian marketThe successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activitiesWe will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. Previous Australian contractor experience will be highly regarded. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. Competitive remuneration package andamp; career growth opportunities available for the right candidate.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager  Pipelines]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDB5E0BEACDBD0876482579EE0000885B</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Project-Manager-Pipelines_1623794.html</url>
<company><![CDATA[Compass Global Resourcing]]></company>
<description><![CDATA[A leading engineering contractor is seeking to recruit a PM/Construction Manager for a pipeline construction project based in Australia. The successful candidate will manage, direct and coordinate all site pipeline activities and be responsible for delivering the project to the client in compliance with all contractual requirements. The Construction Manager will provide adequate resource and expertise to ensure the effective monitoring, supervision and control of the pipeline work being undertaken. They will represent the company and establish good relations with the clients, partners, sub-contractors and local authorities.  To apply candidates must meet the following criteria: -Hold a degree or equivalent in Mechanical Engineering. -Have a proven track record in pipeline construction management. -Have an established background in working on oil and gas pipeline construction projects involving in-depth knowledge of all pipeline activities including site and office exposure. -Possess excellent written and oral skills in English. -Possess excellent organisational, presentation and negotiating skills. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Support Engineer  Australia, Mackay]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob441C44F59DAB7E91482579EE000088A5</referencenumber>
<City></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Product-Support-Engineer-Australia-Mackay_1623803.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Product Support Engineers - Australia, Mackay   COMPANY   Global Mining and Construction equipment market leader has 3 opportunities in Mackay, Australia for Product Support Engineers  JOB SUMMARY The primary role of the Product Support Engineer (PSE) - will be to provide electrical technical expertise and general product support to the Truck Mining Fleet to ensure the best possible productivity and reliability is achieved.  KEY REPONSIBILITIES  Provide electrical expertise and product support to the truck fleet as required Maintain a regular site presence where trucks are operating  Develop and mentor site electrical personnel in particular their skills base, training needs and diagnostics Develop procedures for modifications and truck electrical updates Assist in diagnostics on truck faults Assist in employee training (electrical) Assist in failure analysis of electrical components Repair or re program electrical components Analysis and reporting of truck downloads for both information and failures Develop solid communication with to ensure critical updates are provided and to provide feedback on truck performance. Identify and resolve any truck electrical safety issues Develop a detailed monthly report as required Provide downloads and feedback on truck performance as required by the customer Ensure compliance to all safety requirements, before any Service or Maintenance tasks commence. Promote a high level of professionalism to subordinates colleagues and superiors. Complete projects, tasks and requests as directed by the Technical Support Manager Support an environment of best maintenance practice. Assess the occupational health and safety hazards and risks in the workplace, specifically those relating to work undertaken by your position and ensure appropriate control measures are implemented before undertaking those tasks. Raise occupational health and safety issues   PERSON SPECIFICATION  HNC/ HND in High Voltage Electrical Engineering or Equivalent Significant Experience of HIgh Voltage electrical drives and Inverters Sound technical knowledge of hydraulic and electrical systems  Mobile Plant experience (heavy)  Hold a current drivers license Good communication and negotiation skills Able to work in extreme conditions   PACKAGE  86000 - 108,000  38 hour week plus 12 hours overtime + Relocation + Benefits                  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Project Contracts Manager]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6D29A34CC35F98C1482579EE00008A52</referencenumber>
<City></City>
<Country><![CDATA[KUWAIT]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Project-Contracts-Manager_1624937.html</url>
<company><![CDATA[Digby Morris]]></company>
<description><![CDATA[Project Contracts Manager Ref:NK/(13096)  Digby Morris client are a leading international consultancy, who operate in power, infrastructure, hydrocarbons, minerals and metals sectors. They currently require a Projects Contracts Manager for a major oil and gas project based in Ahmadi, Kuwait.  Projects Contracts Manager Position reports to:Projects Manager  Primary objective  Is permanently assigned to the Projects commercial and contractual management. A comprehensive knowledge of the principles governing all terms and conditions of contracts, Company contracts policies, and the Company industry as a whole, are prerequisites.  Responsibilities  *Responsible for preparation of tender packages for Assigned Projects for the Client approval in Clients standard terms and conditions format and layout. *Responsible for raising requests of contract action once approved by the Client. *Monitors and reports the progress of the tender packages for assigned projects. *Assists the Client in conducting pre-tender meetings, site visits, replies to tenderers queries, preparation of supplementary letters to the ITB, evaluation of tenders, recommendations of award, internal and external approvals for award recommendations, preparation of contract documentation for signature. *Provides close monitoring of construction activities of awarded contracts with reference to areas of possible claims, review of construction contractor correspondence with respect to contractual impact, production of recommended responses by the Client, evaluation of construction claims as well as other related activities enumerated in the contract. *Participates in Company strategic planning for specific projects, i.e., risk assessment, bid/no bid analysis, business plan. *Ensures accuracy and timeliness of contract administration by the assigned Contract Administrators. *Coordinates with affected groups to ensure proper support in contract administration, proposal preparation, and in negotiations. *Reviews requests for proposals particularly to identify risks and terms which may not conform to Company policy. *Negotiates the more difficult, complex, or sensitive issues with client management. *Makes staffing assignments, offers training, reviews work produced, completes performance evaluations and counselling as needed. *Completes other responsibilities associated with this position as may be appropriate.  Skills/experience *Analysis and problems solving *Creativity/innovation *Communications, written and oral *Formal presentation skills *Ability to influence and persuade *BA/BS in Business, Finance.  *15 years of effective post graduation total experience in contract administration within a large, international engineering firm is preferred.   *5 years of total minimum total post graduation experience in oil and gas, refinery, or petrochemical industry. *10 years of minimum experience as Contracts manager in an Engineering Company *To be additional qualified as a Certified Contracts Manager by any reputable professional association *Must also have excellent communication skills for interaction with clients and potential clients and capable of independently negotiating complex contractual issues  Package  The companys employees around the world enjoy a wide range of benefits and highly competitive compensation packages. Our client offers an environment which is much more than just a place to work; its a place where you can put your innovative thinking and business skills into high gear and work alongside other highly intelligent and motivated people. Its a place where you can apply your skills to some of the worlds most challenging, interesting, and meaningful projects worldwide.    About Us  Digby Morris is one of the worlds leading international recruitment companies specialising in property, construction and engineering. To we date have successfully placed people in over 60 countries worldwide. For more information please visit our website at www.digbymorris.com   Follow us online at Twitter and Facebook at:-   http://twitter.com/#!/digbymorrisjobs   http://www.facebook.com/pages/Careers-at-Digby-Morris/29913207594#!/pages/Careers-at-Digby-Morris/29913207594    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Property & Infrastructure Manager]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 30 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob80682363D14AA62F482579EF00730FD3</referencenumber>
<City></City>
<Country><![CDATA[NEW ZEALAND]]></Country>
<postalcode></postalcode>
<State><![CDATA[North Island Tauranga]]></State>
<url>http://www.engineeringjobs.net.au/job/Property---Infrastructure-Manager-A62F48.html</url>
<company><![CDATA[EQI Global]]></company>
<description><![CDATA[Executive leadership role NZs largest and most successful PortTauranga based engineering, infrastructure and property management opportunityThe Port of Tauranga is the natural gateway to and from international markets for many of New Zealands businesses. The Port has the location, strategic partnerships, facilities, infrastructure and the capacity to expand. As New Zealands largest port, the Company is determined to continue to lead, develop and grow through our people and our commitment to the highest quality service. Due to a pending retirement, an opportunity will exist to join the small and integrated executive team as the Property and Infrastructure Manager. Providing strategic leadership, engineering and property management expertise, you will be expected to lead a highly motivated team of professionals to support the development and growth of the business.Reporting to the Chief Executive, the primary focus of the role will be to:Plan and manage infrastructure development and engineering projects to meet the companys strategic and operational needs.Oversee infrastructure maintenance programmes.Manage the companys commercial property acquisition and lease portfolio.Deliver profitable business unit performance by leading a highly motivated and successful team.Contribute to and help drive the strategic direction of the business. The successful applicant will be a chartered professional engineer with a strong background in infrastructure development and property management. You will also be expected to have a track record of developing and successfully implementing strategy, be a proven leader and have strong commercial management and relationship skills. For further information on Port of Tauranga, please visit www.port-tauranga.co.nz.Confidential enquiries can be made to Graham Ewing. Applications for this role close on Monday 21 May 2012. All applications will be acknowledged by email.Website: www.eqiglobal.com  Email: search@eqiglobal.com  Phone: +64 3 377 7793]]></description>
<salary></salary>
<education></education> 
<jobtype>Permanent</jobtype>
<category>Transportation &amp; Warehousing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Operations Manager  Contractor  Resource Sector]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob53AC58375FAC26C2482579F0000389D9</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Operations-Manager-Contractor-Resource-Sector_1633463.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Build and lead your team to successBe part of Australias largest resource projectsPerth based position with attractive packageThis position is with an established top tier contractor with a major presence in Australia and significant operations globally.     Due to continued growth in one of their specialist divisions and internal promotions a need has arisen for an experienced Operations Manager to join the leadership team.     This role is a senior level appointment within the company and will have a significant input into the future success of the business unit.     The projects are Civil, Pipeline and Multidisciplinary SMP packages in the resource sector in excess of and50 million.     It is likely that the right person will have:   15 years experience with top tier contractors Successfully delivered projects in excess of and100m in a project management capacity  Proven ability leading senior level teams in an EPC environment A strong commitment to HSE   The responsibilities of this role are:   Manage a number of Project Managers with a portfolio in excess of and300m+  Developing effective relationships with clients Manage operations to ensure all company standards are being met  We need this Operations Manager to be a very effective communicator. A background in change management would be received well.     This is a Perth based role and our client is offering an attractive package commensurate with the seniority of the position.    Please send your CV to Alex Paterson in ACRWORLDs Oil and Gas Division for review. (Preferably as a word document attachment) Alternately please call 02 8079 0900 for a confidential conversation.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction;Energy &amp; Utilities;Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Maintenance and Reliability Manager]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD20221C18FCC97D1482579F000038B29</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Maintenance-and-Reliability-Manager_1633466.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Attractive growth opportunitiesWell respected companyDevelop and grow existing businessACRWORLD has officially aligned with a well respected Electrical and Instrumentation contractor with over 20 years experience delivering on some of the worlds largest resource projects.     After speaking at length with their senior management it is clear to me why this company continues to grow from strength to strength. The business culture is one of respect and support and allows their people every available opportunity to succeed.     Due to continued expansion in the resource sector we have a requirement for a Maintenance and Reliability Manager to join the expanding operational team.     The position will be responsible for building on their successful delivery to major oil, gas and mining clients as well as developing business at a high level.     We are looking for a Manager with:   10 years experience in senior positions Execution of Maintenance and Reliability Projects Experience and connections at a senior level in Queensland Strong Eandamp;I background - Degree Qualified Resources experience - Mining or Oil and Gas  To be considered for this role please submit your CV to Alex Paterson in our Oil and Gas Team, preferably in WORD format. Alternately for a confidential conversation please call 02 8079 0900.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Development Manager  Global EPC Contractor  Oil and Gas]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCB8B67391DF6CFFB482579F000038B56</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Business-Development-Manager-Global-EPC-Contractor-Oil-and-Gas_1633467.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[World leading contractor (EPC)Top package on offer with KPI incentivesInfluence the Australian business directionOur client is a global player in the resource sector. With a full suite of gas processing services they have been instrumental in the development of world leading Oil and Gas projects.    Offering a full suite of gas processing services including fabrication, construction and commissioning, our client is looking to strengthen their Australian operations to reflect their international market share.    We are currently searching for a Business Development Manager with the ability to strategically grow the company, both in the short and long term. This role forms part of the senior management team and will see you reporting directly into the Australian Business Manager, and managing a functioning sales team of engineers, office support and BD officers.    This position will reward you with an attractive package and the opportunity to get in on the ground floor of a successful companys regional expansion.     To be considered for this role it is likely that you will have:   10 years experience in the Australian LNG sector Understanding of small to major gas operators Been in senior management roles Experience establishing strategic relationships Worked for global companies  For a confidential conversation, please submit your CV (preferably in a Microsoft Word format) or call Alex Paterson on +61 2 8079 0900.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Flow Assurance Team Leader  Oil and Gas]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA22B30D74F98CDDB482579F00020D84E</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Flow-Assurance-Team-Leader-Oil-and-Gas_1633653.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is one of the worldandrsquo;s leading engineering and design consultancies with global operations.   They provide high-end Design and Project Engineering, Assurance and Consultancy to the oil and gas upstream, midstream and downstream environments.  Our client strives for excellence by recruiting the best and harnessing the skills of their people, investing in their career progression and continued development. Our client is currently experiencing increasing demands and requires a Flow Assurance Team Leader to lead all aspects of Flow Assurance Design to meet the technical competency expectations whilst ensuring the companyandrsquo;s reputation for high quality products and delivery is maintained. Based in Perth, Western Australia, the Flow Assurance Team Leader will be expected to deliver on a number of responsibilities which will also include; Contribute to presentations and job bids including estimations, proposals and production of design deliverables all within budget, quality and schedule constraintsProvide QA reports and participate in audits and HAZOPsLiaise with other disciplines to ensure consistent input during all design phases adhering to industry standardExpand Flow Assurance Team capabilities by developing skills and delivering up to date training whilst monitoring / reviewing performance.To be successful in this role you will preferably possess the following; An honours degree in Chemical Engineering or a science degree in Fluid Dynamics. Additional post graduate qualifications would be desirable. Demonstrated experience in the oil and gas industry, with most of this in a multidiscipline design environment.Extensive experience with OLGA dynamic simulatorOperations support and/or process design background highly desirable.Experience in interfacing with production and engineering disciplines in an Eandamp;P operating company environment. Past experience with wax, sand, emulsion, fluid chemistry and CFD analysis is desirable Sound understanding of offshore engineering technology, offshore production operations, fabrication and construction. Experience with developing staff and performance also including review and recruitment. Familiarity with relevant Australian and International standards. If you are looking to be part of a key leadership team with a focus towards client and professional development to the Flow Assurance team, then apply now.       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CSWIP Welding Inspector  Gas Pipeline]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC00F5C6F6280876F482579F00020F4B5</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/CSWIP-Welding-Inspector-Gas-Pipeline_1633728.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Engineering, Construction, Building and Maintenance Company with a global presence and they have ongoing projects throughout the Australasia region.           One of their major Gas Pipeline Construction Projects in Queensland is now seeking the expertise of an experienced Welding Inspector to provide quality control for all welding activities.           You will fly to Central Queensland on a rotation of 28 days on and 9 days off and while on site you will be reporting to the QA/QC Team. Your responsibilities will include (but not be limited to);    Verifying that approved welding procedures, methods and consumables are being used by qualified personnel on all areas of the project.   Verifying that all construction and fabrication activities have been conducted in accordance with procedures and items conform to engineering specifications, design and codes of practice.   Conducting visual inspections of welds and repairs of welds in accordance with procedures and codes of practice.   Monitor Welder repair rates in accordance with job quality requirements.   Provide technical guidance for welding sequence and distortion control in accordance with procedures and job requirements.   Prepare and issue progressive inspection reports and inspection release notes.          In order to be successful it is essential that candidates have;    AUSTRALIAN EXPERIENCEAll relevant welding inspection certificatesPipeline project experienceCertification Scheme for Welding and Inspection Personnel (CSWIP) qualified    Candidates will need to have a keen eye for detail when building premium structures.     This is a fly in fly out role to the project location in Central Qld. Candidates must be prepared to work in a remote location for 28 days on and 9 days off.     An Annual Salary and Site Allowance will be offered to successful candidates.     If you are looking for a role that is different, yet essential within the team, then apply now!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Coating Inspector  LNG Pipeline Project]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob72F7224A71736DE3482579F00020F4D3</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.expatengineer.net/job/Coating-Inspector-LNG-Pipeline-Project_1633729.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is Engineering, Construction, Building and Maintenance Company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  Due to current project expansions, they are seeking an experienced Coating Inspector to join the team on one of QLDandrsquo;s largest pipeline construction project.  Some of the main objectives of the Coating Inspector are; Monitoring daily coating issues, techniques, production results, and assist with management of the coating sub-contractor.Ensure Subcontractors meet their responsibilities and Project requirements.To provide a focal point of contact for Quality function activities for a designated Area. To lead the Quality team allocated to that Area and liaise with the Area Line Supervisors and Managers on day to day Quality issues.Implementation, management and monitoring for compliance purposes, all Quality aspects in accordance with the established policies, procedures, systems and requirements approved by the Company and Client. Coordinating with Management Team to ensure personnel assigned to the Project understand and meet Quality objectives. To ensure adherence to the Project Execution Plan (PEP) and Quality Management Plan / System. To be successful in this role you will have a Coating trade background and be highly experienced in similar projects. It is also required that you have; NACE CertificationExtensive experience in Supervision and Inspection of coating,Past Coating experience in Site Construction,Previous Training experience and management of staff, Possess reasonable knowledge of applicable National and International Codes and Standards, Ability to adapt to Client and other Specifications and Standards as required, Possess sound knowledge of coating techniques and methods, Ability to monitor and drive subcontractor activities in these arenas, Sound computer skills with Word, Excel, and other traceability Database applications. The pipeline construction project runs through central Queensland and you will work on a 28 / 9 roster. It is essential that you have experience working on Gas Pipelines and you have NACE certification.  If this sounds like a good opportunity to you, then apply now!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Recruitment Manager  National role]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF92CE6C78D08844F482579F000353722</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Recruitment-Manager-National-role_1633770.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Mid tier contractor in E and I and civils.Senior level role within the business.Long term opportunity to grow with the companyOur Client, is a very well respected and successful contractor based in Perth.  They are making great progress, winning more and more work in the resources industry. They are now looking to appoint a Recruitment Manager to work across the business.  With a highly experienced executive team, this company has expanded to work across infrastructure, mining and LNG projects in the booming resources sector.      The company has a proven track record for strong relationships with their clients in the industry and have an extremely exciting business plan over the forthcoming years.      The Recruitment Manager will be based in Perth, Australia. They will have a dedicated background in leading and managing an internal recruitment team on site as well as partnering with third party agencies.  Working closely with the HR team to ensure the workforce is supported and implemented at the highest level. The remit covers both blue and white collar workers.     The candidate we want will show strong initiative and demonstrate loyalty to an organisation in Australia.   Ideally the candidate will have experience working for a construction or resources aligned business.    As a reward, the company will have a competitive salary, bonus, along with the opportunity to be part of an exciting phase for a well known company.    They know that every employee has something important to say, and that every employee is integral to the success, appreciation is the best motivation.     It is important to reiterate that the overall projects this company work on are of the highest profile on the global resources platform.       All applications will be treated in strictest confidence - we understand especially in this provision this is paramount.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Tom.Desborough@acrworld.com for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Construction Supervisor  Bridges  Client side  WA]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCF9D7CED2DA4BF40482579F00035CE43</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Construction-Supervisor-Bridges-Client-side-WA_1634357.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Minimum 18 month life cycleClient side project managementPerth based HQWe represent a major international engineering and project management consultancy who are supervising construction of mining infrastructure for a large Australian prospecting organisation. A role is available on the client side supervision team, for an experienced Bridge Engineer to provide professional advice to ensure that railway bridge structures meet all necessary standards.      Your tasks will include:       Development of design, safety and maintenance standards for Bridge structures on the railway element of the project Coordinating detailed phases of structural engineering work Reviewing designs and providing advice to internal / external stakeholders on works associated with bridge structures Successful project delivery (time, budget, quality) in accordance with standards and processes Key involvement in Project Management (scope, time and cost); Ensure adherence to provisions and guidelines of the Quality Assurance system Ensure personal safety and safe working practices across the project. Understand and follow OHandamp;S procedures.      The successful candidate will be a tertiary qualified Structural Engineer with RPEQ and previous experience working on the bridge elements of a complex road or rail project. You will have a high level of experience in the design, documentation and construction of bridges and well-rounded structural engineering capabilities.       Please send your CV to Brian Byrne in ACRWORLDs Rail Division for review (Preferably as a word document attachment)       View hundreds of job opportunities on our website www.acrworld.com  Follow us on twitter        www.twitter.com/acrworld  Follow us on linkedin      http://www.linkedin.com/companies/acrworld-international-search]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction;Transportation &amp; Warehousing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Analyst, France, 1 Year]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCFE79C2DA325DB75482579F0003ABDE4</referencenumber>
<City></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Analyst-France-1-Year_1634330.html</url>
<company><![CDATA[Lawrence Harvey Search and Selection]]></company>
<description><![CDATA[Business Analyst ET Business Project Leader, France, 1 Year +++    Pour le compte de plusieurs client de renom, je suis a la recherche de Business Analyst et Business Project Leader dans le cadre de diffrentes missions sur toute la France (Principalement Paris, Lyon et Toulouse).   1) Business Analyst   - Recueil de besoin et Spcification - Organisation et animation de runion - Connaissances mtier dans diffrents secteurs dactivits  Mission:  - Recueil de besoins et spcifications   Souhaiter: - Anglais (Lu, crit et parle)  2) Business Project leader  - Organiser et mener le recueil de besoin, les tests et la validation de solution fonctionnelle - Organiser et grer des formations utilisateurs - Assurer le suivi utilisateurs et la mise en place de nouveaux processus.  Mission:  - Project leader sur les applications de gestions.  Souhaiter:  -Anglais (Lu, crit et parle)  Pour toutes informations supplementaires, nhesitez pas me contacter.  Alexandre Richaut, Lawrence Harvey  Key skills: Business, Analyst, Business Analyst, Business Project Leader, Project leader, Applications de Gestions, recueil de besoins, specifications, organisations, formations, Paris, Lyon, toulouse, France, French, English, AnglaisLawrence Harvey is acting as an Employment Business in regards to this position.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Control Systems Engineer  Mining in Mackay]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34F9807299F5A926482579F000514C2F</referencenumber>
<City><![CDATA[Mackay]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Control-Systems-Engineer-Mining-in-Mackay_1634331.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in Mackay. The ideal candidate for this role will be someone who has a reliable level of experience in design and project management within the mining and resource industry. You should now be at a level where your management skills are well developed, or you are now ready to expand into this responsibility.     The role of the Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.  The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportExpereince working in Regional Areas5 years industry experience in the Australian market The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; OIS programming and testingElectrical engineering including designProject management activities    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CivilStructural Engineering Manager]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob25DAF3A94D41E745482579F000514C57</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Civil-Structural-Engineering-Manager_1634332.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons and other industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations.  They are currently seeking an experienced Manager who can head the Civil / Structural division within the business, as well as provide technical assistance to the team and engage in business development activities. Preferred candidates will be experienced in the full range of feasibility studies, detailed design and construction.  The responsibilities of the Civil / Structural Manager include, but not be limited to: Manage a Civil / Structural Engineering team in the preparation of feasibility studies, preliminary and detailed designs, and construction.Ensuring all Civil andamp; Structural engineering work complies with statutory and regulatory requirements and company policies and practices.Providing high level technical support for all Civil and Structural engineering work as required.Supervising preparation of documentation for standards, procedures, safe working practices and monitoring regimes in respect of work on or around electrical and instrumentation equipment.Oversee, mentor and develop junior and intermediate Civil and Structural engineers.Perform regular competency assessments of staff team members, develop training and development plans. In order to be successful, candidates will need to have: Professional Degree in Civil or Structural Engineering.Minimum of 15 years experience in the heavy industry, preferably in the mining and hydrocarbons sector.Well-developed management skills and commercial acumen.Excellent communication skills.Excellent people skillsStrong time-management skillsStrong Business Development skills. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the resource industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Control Systems Engineer  Mining & Resources]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5E994E9D7921429E482579F000514C75</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Lead-Control-Systems-Engineer-Mining-and-amp-Resources_1634333.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in West Perth. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer.  The role of the Lead Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 5 years industry experience in the Australian market Candidates will be required to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Provision of technical guidance to junior engineers and peers;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts.    The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activities    We will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pipe Stress Engineer  Mechanical & Piping Engineer   Onshore Oil and Gas]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDF6FADAEE6774201482579F000514C98</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Pipe-Stress-Engineer-Mechanical-and-amp-Piping-Engineer-Onshore-Oil-and-Gas_1634334.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.     Due to ongoing work and an increase in demand, they are now seeking an experienced Mechanical andamp; Piping Engineer with Pipe Stress Engineering experience to join their team in Perth CBD. We are looking for candidates who have experience working on onshore gas plants in Australia.     We are seeking Mechanical Engineers who have a high level of experience in the oil and gas industry and the successful candidate will ideally have the following experience: Piping stress analysis experience in a Consulting / Engineering environment pertaining to Hydrocarbon / Petro-chemical / Oil andamp; Gas sectors.In-depth knowledge in stress analysis and using Caesar IIAdequate knowledge in Piping layout, Design of Supports, Hanger selection etc.Knowledge of dynamic analysis will be considered an added advantage. In order to be successful, candidates will also be required to experience on:    Plot Plans, Piping Layouts,Piping Specifications, Valve specificationsStress AnalysisVendor quote evaluationsVendor quote evaluationsVendor drawing review and approval    In order to be successful, candidates will be required to; Mechanical Engineering DegreeMinimum of 5 years in a similar roleCommercial awareness for project evaluation and submission for approvalClear and respectful communication skills at all levelsHighly developed time and task managementGood understanding of Australian codes and standards    The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the downstream oil and gas industry.     If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Structural Designer  Oil and Gas]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0B0FFB8B2A002C8A482579F000514CBF</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Structural-Designer-Oil-and-Gas_1634335.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.     Due to ongoing work and an increase in demand, they are now seeking an experienced Senior Structural designer to join their team in Perth who are working on an onshore gas plant in Western Australia. Candidates should have a high level of experience in the oil and gas industry and ideally have the following qualifications and experience: Minimum eight years relevant experienceExperience using AutoCAD Version 11 or Autoplant v8iHighly developed technical skillsAbility to work in and manage a small teamCivil and Structural designDemonstrated design experience in Oil andamp; Gas / Hydrocarbon industry experience preferredAustralian experience essentialAustralian citizenship or permanent residency essential The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the oil and gas industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer  Control Systems in Mining & Minerals]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBCDF12545912357E482579F000514CDF</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Project-Engineer-Control-Systems-in-Mining-and-amp-Minerals_1634336.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth and development, they are currently looking for an experienced Project Engineer to join their team in West Perth. Candidates are required to have had some experience in the Mining and Minerals industry and you will be required to provide technical deliverables of a project using your background in Control Systems Engineering.     The successful applicant will also have Proven Technical skills in: Control Systems EngineeringPLC andamp; OIS programming and testingElectrical engineering including designProject management activitiesDiscussions with various stakeholders (site operational people to extract information)Project Engineering through implementation phases of the projectTechnical / Report Writing    You will also be required to assist in the control and monitoring of schedules and financial aspects of a project with the team in liaison with the Project Manager.     We are looking for candidates who are able to display at least 5 years experience in a project engineering role and mining industry experience will be highly regarded.     The role of the Control Systems Engineer will also be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical)High end computer literacyWell developed written and verbal communication skillsSite Commissioning experienceProven record in site support5 years industry experience in the Australian market    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electrical Engineers   Hazardous Area]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE3183EE651A711EB482579F000514D0E</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Senior-Electrical-Engineers-Hazardous-Area_1634337.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[    Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth, development and on-going work, they are currently seeking highly experienced Electrical Engineers from the Oil andamp; Gas and Hydrocarbon industries, who have a strong knowledge of the Hazardous Area. Opportunities exist in both Perth and Brisbane.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and GasDegree or equivalent experience/qualificationsExperienced with Hazardous Area Technical writing and design specification experience Experienced with High Voltage     The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.Produce electrical designs as required.In addition produce instrumentation and control systems designs as required.Carry out electrical testing and associated electrical installation works as required:In accordance with the relevant legislation, and Within the employees competencyAs authorised by the Employer, andSo as to meet project requirements    We are looking for candidates who are able to display at least 5 years experience in Electrical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! Australian experience is necessary!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer  Hazardous Area]]></title>
<date>Mon, 30 Apr 2012 00:00:00 GMT</date>
<Closedate>Mon, 25 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob846C982E29448AEE482579F000514D3A</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Engineer-Hazardous-Area_1634338.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking highly experienced Electrical Engineers from the Oil andamp; Gas and Hydrocarbon industries, who have a strong knowledge of the Hazardous Area. Opportunities exist in both Perth and Brisbane.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and GasDegree or equivalent experience/qualificationsExperienced with Hazardous Area Technical writing and design specification experience Experienced with High Voltage     The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.Produce electrical designs as required.In addition produce instrumentation and control systems designs as required.Carry out electrical testing and associated electrical installation works as required:In accordance with the relevant legislation, andWithin the employees competencyAs authorised by the Employer, andSo as to meet project requirements    We are looking for candidates who are able to display at least 5 years experience in Electrical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! Australian experience is necessary!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Mechanical Engineer]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7598FF58FA75A6C7482579F1000994A7</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Lead-Mechanical-Engineer_1646051.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[Engineer national projectsHobart based positionHigh profile mining clientsThis Australian owned and operated engineering consultancy offers a multi-disciplinary suite of professional services across the construction, industrial, environmental and infrastructure  sectors. With locations throughout the eastern seaboard, they have a strong operational presence in Hobart where they continue to successfully deliver a broad range of national projects.   Reporting to the National Industrial Manager, this role focuses on bidding, winning and delivering industrially focused projects for a growing national client base. Youandrsquo;ll be providing direction and leadership to junior engineers whilst offering innovative design expertise and cost effective project outcomes to clients.   As the successful candidate, you will ideally have consulting experience, coupled with a strong commercial focus and proven design expertise.  Familiarity with mining, mineral processing and bulk materials handling experience projects will be advantageous.   This position is based in Hobart, requires interstate travel and offers excellent remuneration and benefits. Contact Adam Barker at adam.barker@hays.com.au or 03 6234 9554.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Rotating Machinery Engineer - Abu Dhabi (Very Urgent)]]></title>
<date>Tue, 27 Mar 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB6B42DF9D28BF6E9482579F10019059B</referencenumber>
<City></City>
<Country><![CDATA[UNITED ARAB EMIRATES]]></Country>
<postalcode></postalcode>
<State><![CDATA[Abu Dhabi Abu Dhabi]]></State>
<url>http://www.expatengineer.net/job/Rotating-Machinery-Engineer---Abu-Dhabi--Very-Urgent--B05548.html</url>
<company><![CDATA[Consolidated Technical Services]]></company>
<description><![CDATA[Principal Accountabilities * Monitors major Rotating Machinery operational and maintenance data, trends and recommends/implements changes in maintenance strategy as necessary to improve performance. * Performs professional trouble shooting and failure analysis on the failed Rotating Machinery/components and makes recommendations to improve reliability. * Prepares Scope of Work for the contracts/tenders of overhauls of major Rotating Machinery and all technical documents drawings for tendering. Communicates with commercial division to clarify all technical queries raised by the contractors. * Follows up and co-ordinates the implementation of overhauls inspections and repairs contracts related to Rotating Machinery, on site and at the contractor workshops. Evaluates and reviews the performance of the awarded contractors. * Raises and reviews all modification proposals related to major Rotating Machinery, and communicates with Facilities Engineering Division as required. * Co-ordinates with Rotating Machinery manufacturers/OEM to update the associated service bulletins. Keeps site engineers aware of the new manufacturers recommendations and methods of repairs/inspections, and follows up the implementation as necessary. * Raises all requirements of spare parts for Rotating Machinery in coordination with the supervisor in order to achieve the availability of the spares required with minimum possible stock value. Clarifies technical queries raised by spare parts suppliers and recommends alternative solutions accordingly. * Follows up application of HSE procedures rules, regulation, and ensures full awareness of HSE rules by all subordinates/contractors as work progress. * Continuously contacts Rotating Machinery manufacturers/OEM to update the associated service bulletins. Keep site engineers aware of the new manufacturers recommendations and methods of repairs/inspections, and follows up the implementation as necessary. Minimum Requirements * B.Sc. Mechanical Engineering * 6 years post qualification engaged as a field engineer associated with major Rotating Machinery operation/maintenance, and possessing problem analysis and trouble shooting capabilities. * Very good knowledge of English ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Sr. Electrical Engineer - Abu Dhabi (Very Urgent)]]></title>
<date>Sun, 08 Apr 2012 00:00:00 GMT</date>
<Closedate>Sun, 08 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC47F6DAC9B4FE3BA482579F10019059C</referencenumber>
<City></City>
<Country><![CDATA[UNITED ARAB EMIRATES]]></Country>
<postalcode></postalcode>
<State><![CDATA[Abu Dhabi Abu Dhabi]]></State>
<url>http://www.expatengineer.net/job/Sr--Electrical-Engineer---Abu-Dhabi--Very-Urgent--5C1248.html</url>
<company><![CDATA[Consolidated Technical Services]]></company>
<description><![CDATA[Main Accountabilities:* To troubleshoot problems, identify reasons and recommend remedial action to ensure that maintenance services are provided safely and efficiently.* To diagnose, analyze and carry out root cause failure analysis, highlight reasons for equipment failure and advise on remedial measures to avoid failures. Also to study and carry out residual life assessment of critical electrical equipment and suggest corrective action to be initiated by respective area engineers.* To enforce the implementation of company Health Safety and Environment Management System (HSE MS) and also promote awareness of its use among all personnel.* To initiate and review plant change requests as per company procedure to equipment, units and plants. To conduct site engineering studies to determine the feasibility of introducing modification and incorporate the same to increase reliability and efficiency of plant.* To carry out periodical review and advise on updating material stock and directs revision of specifications in light of information from manufacturers including deletion obsolete and incorporation of new items, ensure availability of sparest materials.* To provide support to technical/minor projects for developing scope, executions and commission.* To prepare/review and update maintenance procedures for electrical equipment and suggest procedures to enhance equipment efficiency.* To compile / provide input for preparation of division/department Capital and Operating budgets and monitor annual expenditure budgets.* To develop scope of work for Major over hauls of electrical equipment and work service orders, coordinate implementation with other Sections.Minimum Requirements:* Bachelor in Electrical Engineering or relevant field.* 8-10 years experience in Oil and Gas sector* Very good knowledge of English]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>8 years</experience>
</job>
<job>
<title><![CDATA[Condition Monitoring Technician - Abu Dhabi (Very Urgent)]]></title>
<date>Thu, 26 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 26 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob965C55226B174D9D482579F10019059F</referencenumber>
<City></City>
<Country><![CDATA[UNITED ARAB EMIRATES]]></Country>
<postalcode></postalcode>
<State><![CDATA[Abu Dhabi Abu Dhabi]]></State>
<url>http://www.expatengineer.net/job/Condition-Monitoring-Technician---Abu-Dhabi--Very-Urgent--07DE48.html</url>
<company><![CDATA[Consolidated Technical Services]]></company>
<description><![CDATA[Main accountabilities: To work as Rotating Equipment Inspector for acceptance after major overhaul of small, medium and large rotary equipment such as motors, pumps, fans, blowers, gearboxes, compressors, steam and gas turbines, turbo expanders, etc. Receives verbal or written instructions from the Condition Monitoring Supervisor, obtains requirements for work and permits to work, and proceeds to worksite to carry out the job. Carries out daily inspection and predictive maintenance checks on rotating machinery such as compressors, pumps, gas and steam turbines, blowers, motors etc., as defined by computer maintenance management system. (Maximo), attending other abnormalities being raised by Operations. Performs Condition Monitoring by checking vibrations, temperatures and pressures, checking oils levels and flows. Reports to Condition Monitoring Supervisor where readings are outside tolerable limits. Carries out visual checks of the mechanical seals of pumps for leaks and where applicable arranges for equipment to be stopped in hazardous situations.  Carry out collecting electronic data for the running equipment, IES BN 3500,3300 panels, BN Trendmaster, MMS Data Acquisition units, DCS data, Mark V control system and sub station motors controls system. Carry out borescopic inspection on large rotary equipment like steam and gas turbines and other rotating equipment when needed.  Steam traps mapping, surveillance, traps analysis and raising work orders and generate reports. Daily review and checking of on line monitoring system (Bently Nevada Machinery Monitoring System, Machinery Condition Monitoring and Performance Monitoring) on critical machinery for abnormalities and reporting exceptions to Condition Monitoring Supervisor. Maintaining/ updating history of rotating equipment.  Checks that routine maintenance of machinery and equipment is carried out as required by Maintenance Technicians to ensure smooth running of machinery and equipment. Determines if major equipment or sub-assemblies have to be removed to the workshop for major repairs or overhaul and follow up of equipment repair status.  Carry out inspection, counter check/acceptance of rotary equipment alignment, motor no load run performance at workshop and at site, commissioning and acceptance of rotary equipment after any repairs. Checks that required repairs, replacements and alignments are correctly carried out, and equipment after re-assembly in accordance with requirements. Site acceptance of new equipment based on no load/ load run performance in the project. Releasing punch list for abnormalities of rotating equipment in the project, confirming punch list items after execution by contracts. Operates computer terminal and associated auxiliary devices to perform condition monitoring and vibration checks, raising work orders for abnormalities in Computerized Maintenance Management System (Maximo) after reviewed/approved by Condition Monitoring Supervisor/ Rotating Equipment Section Head. Complies with all HSE regulations, including the use of protective clothing and equipment. Carries out similar or related duties as assigned, such as assisting in, or carrying out modifications to system or the installation of new equipment and machinery, observing good housekeeping and work practices on-site and assisting his Supervisor during the start-up and shut down of critical equipment and other related systems.        Main Challenges: Implement quality standards for old and new facilities of the Company. To complete the job as per planning work schedule. To identify faults and failure. To provide support as requested by Supervisor/ Rotary Equipment Section Head.]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[Subcontracts Coordinator]]></title>
<date>Tue, 28 Feb 2012 00:00:00 GMT</date>
<Closedate>Mon, 28 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobABA542E617A036DA482579F10019133C</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/jobs.nsf/v/3737482579B1005A06A7</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Subcontracts Coordinator for the design and execution of some Oil and Gas projects. The design activity will take place in Madrid offices of our client for about 1 year; the execution will continue in one of the following possible locations: - Canary Islands - Volgograd (Russia) - Bolivia - Canada  Here below there are some details for the Madrid phase: - Location: Madrid, Spain - Starting Date: ASAP - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Salary: Negotiable, depending the profile  Details for the second phase will be made available in the following months  Spanish knowledge, even if not mandatory, will be highly appreciated   ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[OJT Maintenance Instructor]]></title>
<date>Wed, 29 Feb 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob68175F504B6E1A4C482579F10019133F</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/OJT-Maintenance-Instructor-AF3448.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for an OJT Maintenance Instructor, the OJT course is addressed to newly graduated engineers. It takes place in refinery in Italy from 23rd April 2012 to 28th September 2012. The course language is English. Working schedule is 8 hours a day / 5 days a week  ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>15 years</experience>
</job>
<job>
<title><![CDATA[Construction Civil Superintendent]]></title>
<date>Fri, 09 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 09 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3BE293617B70E6AC482579F100191345</referencenumber>
<City><![CDATA[North West Karratha]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Construction-Civil-Superintendent-B14748.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Construction Civil Superintendent for the TAN BURRUP Project in Karratha (Western Australia) Type of plant : Nitric Acid Plant (Module Plant). The project will start in September 2012 with a duration of one year renewable. Profile must have good knowledge of Modules Plants, in case he has experience in Australia projects and YARDS in Australia / South East Asia it would be preferable.]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Construction Mechanical Superintendent]]></title>
<date>Fri, 09 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 09 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC0C62BE86EF92649482579F100191346</referencenumber>
<City><![CDATA[North West Karratha]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Construction-Mechanical-Superintendent-3BBC48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Construction Mechanical Superintendent for the TAN BURRUP Project in Karratha (Western Australia) Type of plant : Nitric Acid Plant (Module Plant). The project will start in September 2012 with a duration of one year renewable. Profile must have good knowledge of Modules Plants, in case he has experience in Australia projects and YARDS in Australia / South East Asia it would be preferable. ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Construction Piping Superintendent]]></title>
<date>Fri, 09 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 09 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob30C659753D147A89482579F100191347</referencenumber>
<City><![CDATA[North West Karratha]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Construction-Piping-Superintendent-4F0948.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Construction Piping Superintendent for the TAN BURRUP Project in Karratha (Western Australia) Type of plant : Nitric Acid Plant (Module Plant). The project will start in September 2012 with a duration of one year renewable. Profile must have good knowledge of Modules Plants, in case he has experience in Australia projects and YARDS in Australia / South East Asia it would be preferable.]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Construction Electrical Superintendent]]></title>
<date>Fri, 09 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 09 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F2C5F3D432C3169482579F100191348</referencenumber>
<City><![CDATA[North West Karratha]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Construction-Electrical-Superintendent-47BA48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Construction Electrical Superintendent for the TAN BURRUP Project in Karratha (Western Australia) Type of plant : Nitric Acid Plant (Module Plant). The project will start in September 2012 with a duration of one year renewable. Profile must have good knowledge of Modules Plants, in case he has experience in Australia projects and YARDS in Australia / South East Asia it would be preferable.]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Construction Instrument Superintendent]]></title>
<date>Fri, 09 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 09 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob310770654C50F6E1482579F100191349</referencenumber>
<City><![CDATA[North West Karratha]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Construction-Instrument-Superintendent-F7C948.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Construction Instrument Superintendent for the TAN BURRUP Project in Karratha (Western Australia) Type of plant : Nitric Acid Plant (Module Plant). The project will start in September 2012 with a duration of one year renewable. Profile must have good knowledge of Modules Plants, in case he has experience in Australia projects and YARDS in Australia / South East Asia it would be preferable.]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>20 years</experience>
</job>
<job>
<title><![CDATA[Asset Integrity Instructor]]></title>
<date>Mon, 12 Mar 2012 00:00:00 GMT</date>
<Closedate>Tue, 12 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob175AE9584BAA7E1C482579F10019134A</referencenumber>
<City><![CDATA[Val dAgri (Basilicata region  southern Italy)]]></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Asset-Integrity-Instructor-1E1348.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for an Asset Integrity Instructor for an OJT course addressed to new graduated engineers. Job location is oil plant located in Val dAgri (Basilicata region  southern Italy). Here below you can see a few other details: - Starting date: 23rd April 2012 - Duration: until 28th September 2012. Its planned a stop of a couple of weeks. - Working schedule: 8 hours a day / 5 days a week. - Rotation: residential ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>15 years</experience>
</job>
<job>
<title><![CDATA[Planning & Cost Control Engineer]]></title>
<date>Wed, 14 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 14 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCA4D88F09ED75889482579F10019134B</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Planning---Cost-Control-Engineer-CA6A48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for an Planning and Cost Control Engineer to be involved in PLI (pipeline) Package of the Zubair Project. First job location is Italy, then after one year the project will be transferred to Zubair Site (Basra, Iraq). In Italy PMC team shall follow up the engineering phase at EPC contractors premises then in Iraq PMC team shall supervise the construction phase at site. Here below you can see a few other details of the period in Italy: Starting Date: 15/04/12 Working schedule: 8 hours a day / 5 days a week Duration: 12 months renewable ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Electrical and TLC Engineer]]></title>
<date>Wed, 14 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 14 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD95178B497E8B891482579F10019134C</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electrical-and-TLC-Engineer-3F6048.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for an Electrical and TLC Engineer to be involved in PLI (pipeline) Package of the Zubair Project. First job location is Italy, then after one year the project will be transferred to Zubair Site (Basra, Iraq). In Italy PMC team shall follow up the engineering phase at EPC contractors premises then in Iraq PMC team shall supervise the construction phase at site. Here below you can see a few other details of the period in Italy: Starting Date: 15/04/12 Working schedule: 8 hours a day / 5 days a week Duration: 12 months renewable ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>15 years</experience>
</job>
<job>
<title><![CDATA[Lead Process Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCF837E71D15D43DE482579F10019134E</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Process-Engineer-818048.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Process Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Project Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE15BED6F06998EE482579F10019134F</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Engineer-F7CB48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Project Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Lead Rotating Equipment Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob90CE9A8ED3F0C4B3482579F100191350</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Rotating-Equipment-Engineer-9E5148.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Rotating Equipment Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8E0475FA19823CA4482579F100191351</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/jobs.nsf/v/E339482579C8003E71A0</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Project Manager for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Lead Structural and Civil Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDBDE1C2C27BDEB92482579F100191352</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Structural-and-Civil-Engineer-088C48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Structural and Civil Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Lead Static Equipment Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob476EDD44677FE6EF482579F100191353</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/A6DC48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Static Equipment Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Lead Piping Design and Material Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDCE68ED471731F62482579F100191354</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Piping-Design-and-Material-Engineer-16C848.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Piping Design and Material Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Procurement Coordinator]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1B9A1042CF6786E4482579F100191355</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Coordinator-2C5648.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Procurement Coordinator for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Lead Planning and Control Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2CD5D5475F76E95A482579F100191356</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Planning-and-Control-Engineer-6C8648.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Planning and Control Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Lead Electrical Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob71E11DA93215FA40482579F100191357</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Electrical-Engineer-093948.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead Electrical Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Lead I&CS Engineer]]></title>
<date>Wed, 21 Mar 2012 00:00:00 GMT</date>
<Closedate>Thu, 21 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob32190D32F8EEC045482579F100191358</referencenumber>
<City><![CDATA[Madrid]]></City>
<Country><![CDATA[SPAIN]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-I-CS-Engineer-5F0948.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking a Lead IandCS Engineer for a job related to the Lukoil refinery of Volvograd, Russia. Project consists in the preparation of all the ITB documentation that will be used by our client to issue a bidding request on the EPC contractors market. Scope of work is to set up all the documentation and deliverables related on the process areas. The following are the units under commitment: -Hydrocracking VGO Unit. -Amine Regeneration Unit. -Sour Water Stripper Unit. -Sulfur Recovery Unit. -Hydrogen Unit. -Catalytic Dewaxing Unit. -Hydrofinishing Unit.  Please find below some other details: - Estimated Starting Date: June 2012 - Location: Madrid, Spain - Working schedule: 8 hours a day / 5 days a week - Rotation: Resident - Duration: 12 months renewable - Engagement: Spanish Labour Contract until end of project  Were seeking personnel with a past work experience in Russian Petroleum  Companies and at least 6 years experience IN THE ROLE within Oil and Gas EPC projects.  Russian Fluency is Mandatory ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 years</experience>
</job>
<job>
<title><![CDATA[Ship Loader]]></title>
<date>Fri, 23 Mar 2012 00:00:00 GMT</date>
<Closedate>Sat, 23 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB00D83FB3C9A1F7482579F10019135A</referencenumber>
<City></City>
<Country><![CDATA[UNITED ARAB EMIRATES]]></Country>
<postalcode></postalcode>
<State><![CDATA[Abu Dhabi Ruwais]]></State>
<url>http://www.expatengineer.net/job/Ship-Loader-C38848.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for nr. 2 Ship Loaders for a project in Ruwais  UAE. Field operators experienced in handling solids by train. In site there is a 110-wagon train that carries 11000 tons (full load) to conveyer belt in order to load the ship. Here below you can see a few other details: -Starting: immediate -Duration: 6 months renewable -Duration: 10 hours a day / 6 days a week -Rotation: 90/15]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Transportation and Logistics</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Drilling Technologies Instructor]]></title>
<date>Tue, 03 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 03 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7C55B29D2530F4E3482579F100191365</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/jobs.nsf/v/F044482579D5004C9B81</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking Instructors for a Training course in Drilling Technologies currently planned in north Italy from June to December 2012.   The principal Topics will be: - Mud/ Drilling Fluids Engineering - Drilling Engineering - Drilling Supervision - Well Site Geology (LOG Analysis, etc...)  The Course will be done in English  Details: - Location: Cortemaggiore, Italy - Scheduled Period: from June to December 2012 - Working Schedule: 8 hours a day, 5 days a week  In your application please specify the topics of interest and the expected availability within the scheduled period  ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[Electrical Designer]]></title>
<date>Wed, 11 Apr 2012 00:00:00 GMT</date>
<Closedate>Wed, 11 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDADE795FD6546A8F482579F100191367</referencenumber>
<City></City>
<Country><![CDATA[MONACO]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electrical-Designer-8FDF48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[We are looking for an Electrical Designer with a deep knoweldge of PDMS and English language to be involved in an international team. Here below you can see a few other details: -Starting date: ASAP -Location: offices in the Principality of Monaco -Working schedule: 8 hours a day / 5 days a week -Duration: 6 months renewable  ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>5 years</experience>
</job>
<job>
<title><![CDATA[Drilling Supervisor/Instructor]]></title>
<date>Thu, 12 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 12 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob32273B7886BBB0F0482579F100191368</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Drilling-Supervisor-Instructor-4E0348.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking an Instructor in Drilling Supervision to carry out the relative session of a course in Drilling and Completion Technologies, currently planned in northern Italy from June to December 2012.  The Course will be done in English to Junior Nigerian and Mozambican Engineers  Please find below some details: - Location: Cortemaggiore, Italy - Training Scheduled Period: from June to December 2012 - Working Schedule: 8 hours a day, 5 days a week  With your application please attach an updated CV with a list of all professional certificates and trainings attended Past experiences as Instructor in this or similar matters are higly considered, please include in your CV as well]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Exploration and Production</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Drilling Engineering Instrucor]]></title>
<date>Thu, 12 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 12 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob62ED8AB37C1C9759482579F100191369</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Drilling-Engineering-Instrucor-A9CD48.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking an Instructor in Drilling Engineering to carry out the relative session of a course in Drilling and Completion Technologies, currently planned in northern Italy from June to December 2012.  The Course will be done in English to Junior Nigerian and Mozambican Engineers  Please find below some details: - Location: Cortemaggiore, Italy - Training Scheduled Period: from June to December 2012 - Working Schedule: 8 hours a day, 5 days a week  With your application please attach an updated CV with a list of all professional certificates and trainings attended Past experiences as Instructor in this or similar matters are higly considered, please include in your CV as well]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Well Site Geology Instructor]]></title>
<date>Thu, 12 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 12 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D507A879212FD24482579F10019136A</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Well-Site-Geology-Instructor-A4E848.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking an Instructor in Well Site Geology carry out the relative session of a course in Drilling Technologies, currently planned in northern Italy from June to December 2012.  The Course will be done in English to Junior Nigerian and Mozambican Engineers  Please find below some details: - Location: Cortemaggiore, Italy - Training Scheduled Period: from June to December 2012 - Working Schedule: 8 hours a day, 5 days a week  With your application please attach an updated CV with a list of all professional certificates and trainings attended Past experiences as Instructor in this or similar matters are highly considered, to include in your CV as well ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Mud/ Drilling Fluids Instructor]]></title>
<date>Thu, 12 Apr 2012 00:00:00 GMT</date>
<Closedate>Thu, 12 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5BCE5A494EFD0CD8482579F10019136B</referencenumber>
<City></City>
<Country><![CDATA[ITALY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/jobs.nsf/v/1784482579DD0059F63D</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were seeking an Instructor in Mud/ Drilling Fluids Engineering to carry out the relative session of a course in Drilling Technologies, currently planned in northern Italy from June to December 2012.  The Course will be done in English to Junior Nigerian and Mozambican Engineers  Please find below some details: - Location: Cortemaggiore, Italy - Training Scheduled Period: from June to December 2012 - Working Schedule: 8 hours a day, 5 days a week  With your application please attach an updated CV with a list of all professional certificates and trainings attended Past experiences as Instructor in this or similar matters are higtly considered, please include in your CV as well]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>10 years</experience>
</job>
<job>
<title><![CDATA[Senior Construction Manager]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 24 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob67F7FCE82596800C482579F100191370</referencenumber>
<City></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Alberta Fort McMurray]]></State>
<url>http://www.engineerjob.us/job/Senior-Construction-Manager--7B6248.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for a Senior Construction Manager to be involved in Oil sands project. Location is Fort McMurray, Alberta, Canada. Profile must have experience in modular construction. This profile is required to start on 7th May. Contracts duration is 2 years.  ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>15 years</experience>
</job>
<job>
<title><![CDATA[Quantity Surveyor  Contract Administrator]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7033953FF51C3FFA482579F10019BF56</referencenumber>
<City><![CDATA[Montral]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quantity-Surveyor-Contract-Administrator_1608281.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is a large firm of chartered quantity surveyors, project managers and construction consultants. They are now seeking an experienced Quantity Surveyor who has good skills and experience of Contract Administration for a role based in Montreal, Canada with site visits to Lac Timmons, Quebec area as required by the project. Although ideally you would speak French and English our client will accept someone who just speaks fluent English. You will need to have done several years of contract administration on any of the following types of projects:- Mining, Power stations, Industrial plants, Oil and Gas, Heavy Civils as this project is an iron ore mine. Our client will accept candidates from Canada, the USA, the United Kingdom, Australia and South Africa. This particular project will be for 18 months to two years and then you can move on to another project. You should have a BSc or Certificate in Quantity Surveying, ideally also be MRICS or similarly qualified. Salary and package is highly negotiable for the right candidate.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Quantity Surveyor  Contract Administrator]]></title>
<date>Tue, 24 Apr 2012 00:00:00 GMT</date>
<Closedate>Tue, 22 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5C3B1C29F659313A482579F10019BF57</referencenumber>
<City><![CDATA[Montral]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quantity-Surveyor-Contract-Administrator_1608280.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is a large firm of chartered quantity surveyors, project managers and construction consultants. They are now seeking an experienced Quantity Surveyor who can Contract or Permanent staff who has good skills and experience of Contract Administration for a role based in Montreal, Canada with site visits to Lac Timmons, Quebec area as required by the project. Although ideally you would speak French and English our client will accept someone who just speaks fluent English. You will need to have done several years of contract administration on any of the following types of projects:- Mining, Power stations, Industrial plants, Oil and Gas, Heavy Civils as this project is an iron ore mine. Our client will accept candidates from Canada, the USA, the United Kingdom, Australia and South Africa. This particular project will be for 18 months to two years and then you can move on to another project. You should have a BSc or Certificate in Quantity Surveying, ideally also be MRICS or similarly qualified. Salary and package is highly negotiable for the right candidate.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Planning Engineer  Oil & Gas]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA73E29DFAECE7DC0482579F10019BF61</referencenumber>
<City><![CDATA[Toronto]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Planning-Engineer-Oil-and-amp-Gas_1623963.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is working closely with a large Oil and Gas Operator. They are now seeking a Planning Engineer to join them in Toronto, Ontario, Canada to work on a range of upstream and downstream oil and gas projects. You will support the delivery and maintenance of consistent and realistic plans and control structures for the project. Understand and monitor the interfaces between assigned project sub-elements and other sub-elements. Develop the activities, logic, resources and progress for the assigned project sub-elements. Comply with the planning and progress monitoring procedures. Conduct the schedule monthly progress update, forecast, critical path and trend analyses for assigned elements, including any impact from interface areas. Provide input to the status reports and ensure that these include the incorporation of approved changes. Liaise with project engineering personnel to assist proper understanding of the key schedule sensitivities and drivers. Assist with identification of alternate approaches to optimise the plans. Know the contract key dates, milestones and plan dates and how they relate to the overall project schedule. Understand the requirements of the contract sections for planning and progress reporting. Review and verify contractors reported progress and incorporate into schedule progress updates. Maintain awareness of critical and sub-critical paths and track float consumption. Utilise the standard tools and processes. Assist in the preparation of input data for benchmarking activities. You must have had a good EPC background and preferably gained some experience with an Operator and you must be fully conversant in the use of Primavera P6 and be able to review and challenge contractor plans and create integrated master plans for major projects. You will need to have an Engineering Degree and / or Certificate as a Planning Engineer or have equivalent experience. You must have at least 6 - 8 years experience of more as a Planning Engineer and have some experience of managing small teams. You will need good communication skills. Rate / salary is very negotiable.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[German speaking Contract Administrator]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6E3C7B927C1DAB6A482579F10019BF62</referencenumber>
<City><![CDATA[Erlangen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/German-speaking-Contract-Administrator_1624925.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is a UK firm of claims and commercial consultants providing quantity surveying, claims and dispute resolution services to a range of clients. They now seek a fluent German speaking Contract Administrator - ideally with either an Engineering or Quantity Surveying background and qualifications for a role on some rail related projects (rolling stock) to be based in Erlangen, Germany. Previous experience of contract administration is essential on other rail, civil engineering or similar projects and fluent written and spoken German is required. This role is permanent staff and there will be the opportunity of working on other types of projects in the future including power station, power transmission etc.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Assistant Quantity Surveyor (Russian speaking)]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD8CF2EC6189E6D64482579F10019BF63</referencenumber>
<City><![CDATA[St. Petersburg]]></City>
<Country><![CDATA[RUSSIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Assistant-Quantity-Surveyor-Russian-speaking_1625026.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client, a firm of multi discipline construction consultants now seeks a Russian speaking Assistant Quantity Surveyor who is almost at APC level or similar or who is recently chartered to join them working on a large construction projects in St. Petersburg, Russia. You must have good experience of working with a firm of chartered quantity surveyors and have gained some experience of cost plans and all other pre and post contract work. You will also need to have gained experience of traditional Quantity Surveying in particular you must have experience of doing Bills of Quantities, value engineering and all round cost management. You will be involved on a range of projects which could include offices, shopping centres, hotels and residential properties. You will also be given support towards becoming MRICS qualified if required]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>3 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Senior Quantity Surveyor (Russian speaking)]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3C58A301439ADA4C482579F10019BF64</referencenumber>
<City><![CDATA[St. Petersburg]]></City>
<Country><![CDATA[RUSSIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Quantity-Surveyor-Russian-speaking_1625027.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client, a firm of multi discipline construction consultants now seeks a Russian speaking Senior Quantity Surveyor who is ideally chartered to join them working on a large construction projects in St. Petersburg, Russia. You must have good experience of working with a firm of chartered quantity surveyors and have gained good experience of cost plans and all other pre and post contract work. You will also need to have gained experience of traditional Quantity Surveying in particular you must have experience of doing Bills of Quantities, value engineering and all round cost management. You will be involved on a range of projects which could include offices, shopping centres, hotels and residential properties. You will need to be able to supervise less experienced quantity surveyors and you will need to have good client facing skills to attend meetings etc.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>3 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Assistant Project Manager (Russian speaking)]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1DA6C89F9F0062E0482579F10019BF65</referencenumber>
<City><![CDATA[St. Petersburg]]></City>
<Country><![CDATA[RUSSIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Assistant-Project-Manager-Russian-speaking_1626381.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is a large international multi discipline firm of construction and engineering consultants working on large building construction projects worldwide. They now have a requirement for an Assistant Project Manager who needs to speak both Russian and also English for a position based in St. Petersburg, Russia. The ideal candidate will have several years project management experience working for a firm of construction consultants, be able to run small projects or assist a senior project manager on larger projects. Projects could include hotels, commercial offices, residential and shopping centres. These could be either new build or refurbishment. You will ideally be Degree qualified with some experience of managing your own projects as an assistant project manager. You should have good knowledge of front end project management for the pre and post contract stages of construction projects and have good IT skills, with an understanding of programming software e.g. MS Project, Primavera etc. You should have excellent communication skills to attend meetings with clients and the professional team. Salary is negotiable according to experience.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>4 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Senior Project Manager (Russian speaking)]]></title>
<date>Sat, 28 Apr 2012 00:00:00 GMT</date>
<Closedate>Sat, 26 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCFF37E320ED1CC87482579F10019BF66</referencenumber>
<City><![CDATA[St. Petersburg]]></City>
<Country><![CDATA[RUSSIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Project-Manager-Russian-speaking_1626719.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is a large international multi discipline firm of construction and engineering consultants working on large building construction projects worldwide. They now have a requirement for a Senior Project Manager who needs to speak both Russian and also English for a position based in St. Petersburg, Russia. The ideal candidate will have a number of years of project management experience working for a firm of construction consultants, be able to run large projects and supervise an assistant project manager on larger projects. Projects could include hotels, commercial offices, residential and shopping centres. These could be either new build or refurbishment. You will ideally be Degree qualified, possibly chartered e.g. MRICS, MAPM or similar with experience of managing your own projects. You should have good knowledge of front end project management for the pre and post contract stages of construction projects and have good IT skills, with an understanding of programming software e.g. MS Project, Primavera etc. You should have excellent communication skills to attend and chair meetings with clients and the professional team. Salary is negotiable according to experience.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>4 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Design Manager  Russian speaking]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD69D13C51F2006F6482579F10019BF67</referencenumber>
<City><![CDATA[St. Petersburg]]></City>
<Country><![CDATA[RUSSIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Manager-Russian-speaking_1645156.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client, a large firm of construction consultants seeks a Design Manager to work in St. Petersburg, Russia. Fluent Russian and English is essential. My client will be working on a range of projects including offices, shopping centres, hotels and residential. Responsibilities may including management of the functional design team, agreeing of design budget, dealing with contractors, design checking and monitoring of design for site etc. You will ideally have a Civil Engineering degree, possibly be chartered, have good experience in a similar role, have good communication skills and be able to deal with the professional teams and the contractors for design queries etc. You should also have some experience of supervising other design staff. Salary is negotiable.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Cost Engineer with SAP experience]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob65B20F874CE2D5FC482579F10019BF68</referencenumber>
<City><![CDATA[West London]]></City>
<Country><![CDATA[ENGLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Cost-Engineer-with-SAP-experience_1645154.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client, a large firm of construction and engineering consultants has an urgent requirement for an experienced Cost Engineer who has specific experience in the use of SAP to join them on a long term contract basis in West London. You will work as part of the procurement and project controls team. The project is an open cast iron ore mine overseas but there will not be a requirement for travel as you will be based in London offices. You will need to have experience of sourcing international suppliers for either a mining, oil and gas, power or similar industrial project and making full use of SAP. You must be able to manipulate the SAP system rather than just inputting into it. You are likely to have a BSc in Quantity Surveying, Engineering or similar and you must have a number of years experience as a cost engineer using SAP. This is a contract role for 12 months or longer, working 8 hours per day. Rate is negotiable.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Quantity Surveyor  Fluent French speaking]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBBE14648E9CFE4E0482579F10019BF69</referencenumber>
<City><![CDATA[Paris]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quantity-Surveyor-Fluent-French-speaking_1645152.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[My client, a firm of chartered construction consultants working on both cost and project management for a variety of clients now has a vacancy for an experienced Quantity Surveyor to join their office in Paris. You must have fluent French, ideally English too, and the ideal candidate will have worked for another firm of construction consultants doing the full range of both Pre and Post contract quantity surveying work. You will be involved in cost plans, feasibility studies, contract administration, cost reporting etc. right the way through projects to handover to client. Projects are varied and will include corporate real estate, e.g. offices, banks etc. plus mixed use, hotel / leisure, retail, residential and some industrial projects. You should have a Degree or Diploma in Quantity Surveying, Construction Economics or similar and also have good client facing skills and be computer literate. You will also possibly be MRICS or similarly qualified. Good prospects on offer for the right candidates with this growing office.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Project Manager  Fluent French speaking]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5EBDCE729FFF870B482579F10019BF6A</referencenumber>
<City><![CDATA[Paris]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager-Fluent-French-speaking_1645153.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[My client, a firm of chartered construction consultants working on both cost and project management for a variety of clients now has a vacancy for an experienced Project Manager to join their office in Paris. You must have fluent French, ideally English too, and the ideal candidate will have worked for another firm of construction consultants doing the full range of client based Project Management work. You will be involved in the full range of Front end project management, chairing meetings, selection of professional consultants and contractors, contract administration etc. right the way through projects to handover to client. Projects are varied and will include corporate real estate, e.g. offices, banks etc. plus mixed use, hotel / leisure, retail, residential and some industrial projects. You should have a Degree or Diploma in a Construction / Built Environment subject and also have good client facing skills and be computer literate. You will also possibly be MAPM, MRICS or similarly qualified. Good prospects on offer for the right candidates with this growing office.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Principal Track Designer  WA  International Engineering Consultancy]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8B40E54A7A68EB9C482579F1001F4C0D</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Principal-Track-Designer-WA-International-Engineering-Consultancy_1646398.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Track design leaderLarge heavy haul and passenger developmentsDomestic and International ProjectsThis role offers leadership responsibilities within a respected international engineering and project management consultancy. Your career goals will be fostered within a fluid structure that encourages collaboration and values initiative. Opportunities to work on international projects as well as projects within the busy Australian Rail market will make this a stimulating and challenging role.     Your initial focus will be to act as Principal engineer or project manager on various projects as required. It will be your responsibility to undertake checking and approval of reports and drawings before issue. You will Report regularly to the project director or rail infrastructure manager on project performance and provide feedback to other line management as required.   You will contribute to and manage the technical outputs and quality assurance aspects of projects. You will promote quality improvement and ensure business principles and systems are adhered to with regard to project delivery. It will also be expected that you will mentor and manage a team of engineering support staff, and conduct appraisals and career development reviews for these people.   You will also contribute to overall business development targets by fostering good client relationships. This will be achieved through consistently high standards of project delivery and correspondence. You will also contribute to or manage the preparation of bids/proposals when required.      As the companies business interests will be focused largely on the resources industry in Western Australia, a strong network of contacts within this industry is essential. A degree in Civil engineering or an appropriate discipline is also essential. Chartered Engineering status, or being in a position to achieve this quickly is also required. Project management registration will be an advantage.         Please send your CV to Brian Byrne in ACRWORLDs Rail Division for review (Preferably as a word document attachment)      View hundreds of job opportunities on our website www.acrworld.com  Follow us on twitter        www.twitter.com/acrworld  Follow us on linkedin      http://www.linkedin.com/companies/acrworld-international-search]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transportation &amp; Warehousing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Structural Engineer]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 26 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF70597BE13732EB7482579F100288111</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Structural-Engineer_1646553.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an independent, Australian owned and operated company providing engineering consulting and project management services to the Hydrocarbon industry. Their Engineering capabilities including planning, development and delivery of new projects and the optimisation, modification, operation and maintenance of existing facilities in the energy and resource sector.  Due to ongoing work and an increase in demand, they are now seeking an experienced Senior Structural Engineer to join their team in Perth who are working on an onshore gas plant in Western Australia. The successful candidate will ideally have the following qualifications and experience: Bachelor of Engineering (Civil/Structural)Minimum eight years relevant experienceAn emphasis on structural engineering with exposure to civil engineeringHighly developed technical skills in structural steelConcrete design skillsDemonstrated engineering experience in Oil andamp; Gas / Hydrocarbon industry experience preferredAustralian citizenship or permanent residency essential The remuneration is competitive and will be offered based on your skills and experiences. This role provides a development opportunity for you in the team as our company continues to grow internationally. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the oil and gas industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[German speaking Quantity Surveyor]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5C34BBFFB962AD75482579F10034696C</referencenumber>
<City><![CDATA[Frankfurt am Main]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/German-speaking-Quantity-Surveyor_1645176.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[My client is a medium to large sized firm of chartered quantity surveyors and project management consultants working across the UK and Europe. They now have an urgent requirement for an experienced and ideally chartered Quantity Surveyor to work in Frankfurt am Main, Germany. It is an absolute necessity that you speak FLUENT GERMAN and ENGLISH for this position as the client is German. The initial project you will be working on is the refurbishment of a major hotel. The ideal candidate will have both pre and post contract cost management experience and have a Degree in Quantity Surveying or similar built environment subject and possibly be MRICS qualified. Ideally you will have previous experience of working in Germany although fluency of the language is more important. Candidates from a private practice firm of quantity surveyors will be preferred to contractors surveyors.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Cognos Transformer  France]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34EFCC7C1590D64B482579F100346AFD</referencenumber>
<City></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Cognos-Transformer-France_1647002.html</url>
<company><![CDATA[Lawrence Harvey Search and Selection]]></company>
<description><![CDATA[1.Dfinition gnrale du poste Le poste de dveloppeur Bases de donnes a pour rle dapporter au sein de lquipe informatique, des comptences techniques fortes dans la conception et la mise en uvre de solutions proposes par ORACLE, SQL Server et COGNOS Transformer.  Comptences techniques fortes car il aura  intervenir sur plusieurs projets avec une totale autonomie. Un trs bon relationnel et une grande implication et surtout une autonomie technique sont absolument obligatoires.  La maitrise de langlais  lcrit comme  lORAL est un critre liminatoire.  2.Les activits principales Grce son expertise technique, son sens de lorganisation et son respect des procdures dfinies, il devra tre  mme dintervenir sur les diffrents projets sur les diffrentes technologies.  Etre force de proposition pour complter, amliorer et adapter les procdures actuelles. Intervenir lors de la conception technique des solutions  implmenter.  Etre rigoureux dans la rdaction de documents fonctionnels et techniques qui devront couvrir lintgralit de son champ daction.  Etre actif dans le processus de capitalisation interne des connaissances et notamment assurer un partage des  Best pratices  entre les diffrentes quipes et tre capable de former le reste de lquipe sur les solutions implmentes.    Participer aux nouveaux projets et implmentation afin den dfinir les points cls et/ou de vigilance en matire dexploitation. En relation constante avec le service Exploitation, il doit tre en mesure de conduire la rdaction des fiches techniques qui seront utilises lors du suivi des solutions mises en uvre.  Respecter lapplication stricte des procdures internes et europennes lors de ses diffrentes tches.   3.Autre contribution pouvant tre attendue Conduite dateliers de travail avec les utilisateurs afin de dfinir les demandes, attentes et souhaits  Rdaction du cahier de charges + Documentation fonctionnelle dtaille.  Conduite dateliers de travail avec les quipes techniques afin didentifier toutes les tapes de la mise en uvre technique  Rdaction de la documentation technique dtaille.  Ralisation de tests lors de nouvelles implmentations ou modifications dans les systmes ou existants. Lawrence Harvey is acting as an Employment Business in regards to this position.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Senior Project Manager  Transmission Lines]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8DB59BFF7C22D4A6482579F1003BE232</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Project-Manager-Transmission-Lines_1646855.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Top tier power transmission contractorMajor 130km projectFly in fly outThis company is a top tier engineering, construction and services company within the Australian power sector.  It combines a major business in operations and maintenance of power generation and Tandamp;D assets with EPC contracts on large scale infrastructure projects.    Due to a large scale project opportunity to design and construct a 130km transmission line in WA they now seek a suitably qualified project manager.  You will have full responsibility for the project from engineering and procurement through to construction and commissioning.    The line is part of a larger mine expansion project  which is set to become one of the largest iron ore developments in Australia.    The role will be on a FIFO basis and comes with a significant salary package and generous site uplift.    You must be tertiary qualified in a relevant engineering discipline with extensive experience in the project management of greenfield transmission line projects.  You will have delivered large scale transmission line projects safely, on time and within budget.      Please contact:  Rob Lawrence  02 8079 0930]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction;Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Safety Advisor  QCLNG  Onshore Gas Pipeline]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 26 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob00D8994CDA21E2CE482579F10044667E</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Safety-Advisor-QCLNG-Onshore-Gas-Pipeline_1646973.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in building, mining, oil and gas, petrochemical, power, transport, water and public infrastructure, and they have ongoing projects throughout the Australasia region.  They are currently seeking an experienced Safety Advisor who has had experience within Construction, Fabrication and Maintenance engineering around the Oil and Gas industry. You will be required to work a 28 / 9 rotation during the construction of this project.     Reporting to the Projects Health andamp; Safety Manager your primary responsibility will be to coordinate and advise the day to day Safety function of nominated project sites in partnership with the site leadership team. In addition you will also be required to monitor site performance against safety targets and key performance indicators, conduct calibration and testing of equipment, liaise with organisations to gather safety and equipment related information and conduct inductions, toolbox meetings and training.  Your role will also include, but not be limited to: Coordination and implementation of Safety strategies and initiatives;Prepare and develop safety management plans and other project specific Safety documentation as required by clients and/or legislationCoordinate the collection and review of safety information to the HSE Manager as required To be successful in securing this position it is expected that you posses an OHS / HSE Degree or Diploma or have a Certificate IV, with at least 5 years experience in a similar role. Previous exposure within the construction or heavy industry is essential.     Your experience working on onshore oil and gas systems, construction projects and HSE management will be highly regarded.  A strong track record in implementing practical Safety standards is highly desirable. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Controls Engineer  Onshore Oil and Gas]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 26 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD1A5BBA9838F5A86482579F1004466B4</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Project-Controls-Engineer-Onshore-Oil-and-Gas_1647131.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our Client is an outcome focused project management service provider specialising in project feasibility, management and completion services to the midsize Gas and Energy sector.     In response to increased project activity we are seeking a suitably qualified and energetic Project Controller to join this Oil and Gas Project Services Group.     The successful candidate will ideally have; Strong experience in Cost ControlExperience in an EPCM environmentEngineering Degree or equivalent would be preferable.Strong report writing experienceFive years industry experience Estimating and Budgeting experience Relevant experience in Planning and Scheduling     We are looking for experienced candidates with well developed communication skills. Candidates with Australian experience will be highly regarded.   If this sounds like you, we welcome your application.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Project Engineer]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 26 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob25EB5EB0CE3CF324482579F1004466DC</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mechanical-Project-Engineer_1647132.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our Client is an outcome focused project management service provider specialising in project feasibility, management and completion services to the midsize Gas and Energy sector.   Ideal candidates will have worked on projects such as pipelines, gas processing plants, gas pipeline facilities, power generation facilities, hydrocarbon production and processing facilities, and more.   To be successful for this position you will need to hold a Bachelor of Engineering Degree and will ideally have 10 years relevant experience.     Your responsibilities will include but not be limited to; Monitor project performanceAid in preparation of project cost reportsReview shop drawingsConduct project engineering relating to specific jobRationalisation of engineering works associated with the projectLiaise with sub contractors regarding project related matters.Ensure Quality Standards are maintained    With large scale projects lined up for 2012 and beyond this role can offer longevity and stability. If this is sounds like you, we would welcome your application.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mobile Plant Diesel Mechanic  Australia]]></title>
<date>Tue, 01 May 2012 00:00:00 GMT</date>
<Closedate>Tue, 29 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob55491D3532C2BC58482579F100495D03</referencenumber>
<City><![CDATA[Edinburgh]]></City>
<Country><![CDATA[SCOTLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Mobile-Plant-Diesel-Mechanic-Australia_1647197.html</url>
<company><![CDATA[Acorn Recruitment]]></company>
<description><![CDATA[Diesel/Plant Fitter - Australia  Acorn is working in Partnership with a leading Industrial and mining services company at Various locations in Australia, we currently have opportunities for Diesel/Plant fitters to work on a fixed term 3 year basis in Australia, with very strong possibility of these roles becoming permanent.   Purpose of Position:  Repair and maintenance of Mobile Plant and equipment, to achieve maximum equipment availability and productive life through preventative maintenance. Ensure that all work and tasks are conducted in a safe manner, and that work practices minimise risk.   Person Specification    Timed served Apprentice is essential   Heavy earthmoving repair and maintenance industrial experience.   Up to date mechanical knowledge with heavy haulage and earthmoving equipment.   Good written and spoken communication skills, and the ability to work at various levels  role   Carry out repairs and maintenance on all mobile equipment and fixed plant, in accordance with manufacturers specifications   Troubleshoot and resolve maintenance problems as they occur.   Support and embrace a preventative maintenance system.   Complete all work orders accurately.   Complete all fleet records so that effective reporting and scheduling may be maintained.   Identify and assist in purchasing parts.   Ensure all work is to a high standard.   Create and maintain a high standard of workshop and yard housekeeping   Able to take directions from Maintenance Manager and representatives.   Work with and communicate with other team members effectively.   Ensure that safety concerns are paramount above production issues and immediately report any near misses, injuries, accidents or non-conformance to the Shift manager.   Carry out tasks in accordance with Policies, Procedures, Work Instructions   Package:  42,000 - 79,000 per annum, full benefits package including, 9% pension contribution, free flights, assistance with accommodation , support to complete visa and transfer from UK to Australia    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Analyst  fluent Spanish & English]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob41175DC79D377CF4482579F100626090</referencenumber>
<City><![CDATA[Vancouver]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Business-Analyst-fluent-Spanish-and-amp-English_1651404.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[My Client is a leading  multinational with considerable experience within the mining industry. Their name is universally recognised and the company is enjoying a sustained period of ongoing growth. They now require a Bilingual SPANISH / ENGLISH SPEAKING Senior Business Analyst to join their team. In Vancouver Canada.  Working with global leaders in mining, you will support the implementation of production and productivity management software at client sites, analysing and integrating client processes with product capabilities and you must an extensive knowledge in this field. You will bring your strong project management, prioritising, and consulting skills as you manage multiple projects while providing expert advice and training services to clients.  Duties Scoping, Solution design, Implementation of project solutions: Develop product customisations in line with client requirements: Support to Junior consultants : Quality testing of product upgrades and add-ins: Training course design and delivery  Ideally, you will have the following mix of qualifications and experience to succeed in the role: Formal qualifications in IT :Experience in implementation of Enterprise systems :Project management experience : Consulting or other customer-facing experience Demonstrated proficiency in Microsoft SQL Server : Software development experience : Excellent communication and organisational skills : Prior study or exposure to mining / mineral processing industries is essential In return, you will be offered a position with a leading name within the mining industry including travel and further career advancement opportunities. An attractive remuneration package will be offered in line with experience along with bonuses based on company profit.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Consulting and Corp. Strategy</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Senior Planner(Corporate)]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFC1D5CFFEBBFC4F7482579F10081FFDE</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-PlannerCorporate_1652877.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Salary PackageGreat Career ProspectsLarge Scale Projects Senior Project Planner - Corporate Role      Our Client is an innovative contractor specialising in the non process infrastructure for the Resource/LNG industry. Due to vast growth, they are looking for a number staff, including a Senior Project Planner.       The company purely works in the booming resources sector on the LNG and Mining remote projects throughout Australia.  The company has a proven track record for strong relationships with their clients in the industry resulting in return work after each project.     The Project Planner will be based in the companies Perth office. They will have a dedicated background in resource construction. The candidate will be able to lead a team of workers and have good a disciplined manner, as well as consistency on their workload with no issues in what they do. They will show strong initiative and demonstrate loyalty to the projects. The candidate will have minimum of 5 years experience in the industry and have proven senior experience, working on large scale projects.      As a reward, the company will have a competitive salary and provide a solid platform to develop your career.    We know that every employee has something important to say, and that every employee is integral to their success, appreciation is the best motivation.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression Of Interest Planners]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob473AEE85B34DB944482579F100820059</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-Of-Interest-Planners_1652878.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsMajor ProjectsGreat Salary PackageACRWORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planners, Planning Engineers, Planning Managers and Project Planners .    ACRWORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.      In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Engineer (WEST COAST)]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE3B7872C81ED688B482579F100820087</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Engineer-WEST-COAST_1652879.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsGreat Salary PackageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Engineers    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Engineer (East Coast)]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9BEF7FBF470628CD482579F1008200B6</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Engineer-East-Coast_1652880.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectGreat Salary PackageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Engineers.    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expression of Interest Planning Managers]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAABC398CE9020039482579F1008200F1</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expression-of-Interest-Planning-Managers_1652881.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProgressionGreat Salary packageLarge Scale ProjectsACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Managers    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Expressions Of Interest Planning Manager (EAST)]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob373B98EF61CD3179482579F10082010E</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Expressions-Of-Interest-Planning-Manager-EAST_1652882.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Great Career ProspectsGreat Salary PackageLarge Scale Projects   ACR WORLD specialise in supplying mid to top tier Engineering and Construction professionals into industry.  With an increasing need for highly skilled personnel across landmark hydrocarbon projects, Australia has become an extremely exciting country to work in and a global front runner within the industry.     At this stage, expressions of interest are now being sought for professionals across the board within the LNG area including (but not exhaustive); Planning Managers    ACR WORLD are partnering with a top tier EPC organisation to ensure the best professionals are identified for such a high calibre project.     To be successful in this role it is likely that you will have:     andbull; Worked with top tier contractors  andbull; Have worked with Primavera 6 (a pre requisite)   andbull; Had experience on multi-discipline projects in the resource sector  andbull; Come from a Civil / Structural, or Mechanical background  andbull; Extensive level of experience in resource led developments        In return, our client is offering a highly competitive negotiable package in addition to a generous uplift component. A strong career path and the opportunity to progress will naturally be on offer with the scope and scale of this project moving forward.      It is important to reiterate that the overall project is one of the highest profile in the world and a great opportunity to step up within the LNG and Oil and Gas industry.     All applications will be treated in strictest confidence.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Matthew Brewer for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining & Materials Handling Mechanical Design Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEEB4DE42FCC463F0482579F200203C63</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-and-amp-Materials-Handling-Mechanical-Design-Engineer_1653536.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking a Mechanical Design Engineer who has had experience working on Mining and Infrastructure or Materials Handling related projects, to join the team based near the Perth International Airport.   The ideal candidate will need to demonstrate: Experience in mechanical design and project management in the mining industryKnowledge and good understanding of materials handling projects  In order to be successful, candidates will be required to display; Bachelor of Mechanical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety;  The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining & Materials Handling Mechanical Design Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9E9F3D08B6DA3303482579F200203C80</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-and-amp-Materials-Handling-Mechanical-Design-Engineer_1653537.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.        They are currently seeking a Mechanical Design Engineer who has had experience working on Mining and Infrastructure or Materials Handling related projects, to join the team based near the Perth International Airport.     The ideal candidate will need to demonstrate: Experience in mechanical design and project management in the mining industryKnowledge and good understanding of materials handling projects    In order to be successful, candidates will be required to display; Bachelor of Mechanical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety;    The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining & Materials Handling Mechanical Design Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5B5EABD58DCE421A482579F200203C9E</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-and-amp-Materials-Handling-Mechanical-Design-Engineer_1653538.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking a Mechanical Design Engineer who has had experience working on Mining and Infrastructure or Materials Handling related projects, to join the team based near the Perth International Airport.   The ideal candidate will need to demonstrate: Experience in mechanical design and project management in the mining industryKnowledge and good understanding of materials handling projects  In order to be successful, candidates will be required to display; Bachelor of Mechanical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety;  The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Estimator  Underground Mining Services]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4033A96D6D331BA8482579F200203CBC</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Estimator-Underground-Mining-Services_1653619.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   As part of ongoing expansion, a position has become available for a qualified and experienced Electrical Estimator to join their team located near Perth International Airport.   The ideal candidate will be required to provide accurate estimates of the total cost of allocated projects. Experience estimating in the electrical discipline within the construction and/or industrial sector will be highly regarded.   The Key Duties will include however not be limited to: Production of realistic but economical project cost estimates for the preparation of major feasibility studies and tenders Preparation of bids, selection of vendors or subcontractors, and determining cost effectiveness Conducting special studies to develop and establish standard hour and related cost data or effect cost reductions. Maintenance of the electrical cost databaseParticipating in regular estimate reviews Preparing presentation/reporting formats for cost/estimate information as required   You will need to be able to work autonomously as well as collectively as a team to meet project goals, have an enthusiastic and proactive approach and take pride in the quality of your work.   Previous estimating experience at a senior level with a thorough knowledge of engineering and construction processes in the mining/resource development of minerals processing industry is essential. The Successful Applicant will also need to meet the following criteria: Good overall computer skills including Word and Excel, and the ability to pick up new systems quicklyOrganisational, time management and communication skills. A high degree of professionalism with customers; strong communication and interpersonal skills Be capable of measuring electrical documentation and producing bill of quantities; Be customer-focused and demonstrate proficient communication and business writing skills; Be capable of identifying and valuing variations; and Be prepared to price or assist in the valuation of variations and financial claims. If this role sounds like your next job than apply now!!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer    Mining Services]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob14D89D6D50500C13482579F200203CE6</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Engineer-Mining-Services_1653620.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   They are currently seeking an Electrical Engineer who has had experience working on Mining and Infrastructure related projects, to join the team at the office located at the International Airport. Ideally, the Electrical Engineer will want to grow and develop with the company as there are many opportunities for career development.   The ideal candidate will have demonstrable experience in:The electrical design relating to underground mining infrastructure, including the equipment such as crushers and conveyors;The supervision of a team of Engineers;A strength in Design with experience in Project Management.At least 4 years + LV Switchboard design and motor control centres experience  In order to be successful, candidates will be required to display; Bachelor of Electrical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety.  Candidates will be required to have minimum of 5 years experience in similar role and previous experience in a Contractor environment will be highly regarded.   To be successful, you will need to have project management and supervision experience, preferably with a contractor. The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer    Mining Services]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2665D5E943D145AA482579F200203D05</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Engineer-Mining-Services_1653621.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking an Electrical Engineer who has had experience working on Mining and Infrastructure related projects, to join the team at the office located at the International Airport. Ideally, the Electrical Engineer will want to grow and develop with the company as there are many opportunities for career development.    The ideal candidate will have demonstrable experience in:The electrical design relating to underground mining infrastructure, including the equipment such as crushers and conveyors;The supervision of a team of Engineers;A strength in Design with experience in Project Management.At least 4 years + LV Switchboard design and motor control centres experience    In order to be successful, candidates will be required to display; Bachelor of Electrical Engineering;Minimum 5 years experience on Mining related projects;Good interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities;A commitment to safety.    Candidates will be required to have minimum of 5 years experience in similar role and previous experience in a Contractor environment will be highly regarded.     To be successful, you will need to have project management and supervision experience, preferably with a contractor.  The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Subsea Pipeline Team Lead]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob41E4FB6727497328482579F200203D29</referencenumber>
<City><![CDATA[PERTH]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Subsea-Pipeline-Team-Lead_1653622.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Atkins is one of the worldandrsquo;s leading engineering and design consultancies with global operations.   They provide high-end Design and Project Engineering, Assurance and Consultancy to the oil and gas upstream, midstream and downstream environments. Atkins strives for excellence by recruiting the best and harnessing the skills of their people, investing in their career progression and continued development. Our Subsea department requires the expertise of a highly motivated Team Lead to lead the team through successful project delivery and outstanding performance across various project stages. The role will be responsible for providing services across such phases as conceptual / feasibility / pre-FEED, front end studies, detailed design and operations. As Discipline Head for Subsea Pipeline you will take lead in developing and maintaining relationships inhouse and with clients being the focal point, whilst providing technical expertise to current projects, potential bids and corporate initiatives In addition to this role you will also be responsible for: Develop the strategy for the Perth Subsea business in accordance with local and global.Develop marketing opportunities for subsea services including presentations, pre-qualification and proposalsDevelopment of the subsea team with mentoring, knowledge-sharing initiatives and performance assessments and recruitmentTo be successful for this role the outstanding candidate will posses the following: Honours degree in related Engineering discipline or equivalent and additional related post graduate qualifications would be desirableProven Experience of successful delivery of subsea Oandamp;G pipeline engineering key aspectsExemplary technical competence in all aspects of subsea and pipeline design and challenges associated to local environment conditions. In addition, experience of deepwater HPHT pipeline would be advantageousAbility to supervise and people-manage a team and be recognised locally for effective high performance and project deliverySound understanding of industry engineering technology, production operations, project execution along with Australian and International standards and codesIntegrity and effective communication skills across all levels and the commercial awareness to appreciate clientsandrsquo; business risk driversStrong focus on HSE and QAThis is a rare opportunity to be recognised in the market for your high valued work and expertise with your team. You will be presented with opportunities and new challenges along with competitive remuneration and flexible leave arrangements. If you are interested in joining this well known market leader that is committed to helping its employees reach their potential then apply now.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Controls Systems Engineer  Mining Sector]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6F56E893932ED457482579F200203D74</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Controls-Systems-Engineer-Mining-Sector_1653623.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   Due to growth and development, they are currently seeking an experienced Control Systems Engineer to join the team at their offices located near the Perth International Airport. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer within the resources sector, in particular mining. The successful applicant will ideally possess: Bachelor of Engineering (Electrical) Experience in Project Management, preferably within the mining sector Experience working on proposals and TendersHigh end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 7 years industry experience Experience working in the Australian marketThe successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activitiesWe will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. Previous Australian contractor experience will be highly regarded. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. Competitive remuneration package andamp; career growth opportunities available for the right candidate.   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mining Engineer  Underground Operations]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6B4730A59E3D367F482579F200203DAB</referencenumber>
<City><![CDATA[West Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Mining-Engineer-Underground-Operations_1653624.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.     They are currently seeking a Mining Engineer who will be responsible for the effective application of mine planning processes, verification of contractual activity, assess the effectiveness of mining performance, reviewing cost performance of mining operations.     The responsibilities of the Project Mining Engineer will include (but are not limited to); Develop and implement mine planning systemsDevelop and implement short term mine scheduling to support operational performance.Prepare the data required for day works claims and monthly claims.Maintain client relationships, offering technical solutions to site and client issues.Support efficient mine planning and contractual claims.Manage the efficient supply of external products and services to support the operation.Provide a technical contribution to initiatives and other projects . In order to be successful, candidates will be required to display; Bachelor of Mining Engineering;Minimum 3 years experienceGood interpersonal and management skills;Excellent communication skills;Strong leadership skills and abilities; andA commitment to safety. Candidates who have had experience underground will be highly regarded. Previous experience in a Contractor environment will also be advantageous.        The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Underground Mining  Senior Project Manager]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6E3EEE7FE4EB9FE2482579F200203DC7</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Underground-Mining-Senior-Project-Manager_1653625.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[The Company Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   The Role They are currently seeking an experienced Project Manager required to manage operations in WAs norhtwest. The ideal candidate will have a well developed understanding of Underground Mining operations and have be able to demonstrate a high level of experience in Project Management, preferably with Contractor organistions. Reporting to the Operations Manager, the Project Managerandrsquo;s role will include acting as the overall Site Manager; ensuring consistent standards are met and be the main point of contact for the client.     The Requirements As the successful candidate, it is essential that you possess the following skills and experience: Tertiary Qualifications Mining Engineering or Management or related areaConsiderable experience in mine management, shotcreting and shaft lining and managing large mulit million dollar projectsPrevious leadership experience over a variety of departments including project control, commercial, ops readiness, HSE, and engineering.A passion for achievement through team building and culture A demonstrated focus and commitment to commercial imperatives and the time critical elements of successful mine operations.    The Rewards The position offers a competitive remuneration of up to and200,000 to and220,000 base salary pa and the work is challenging. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Underground Mining  Senior Project Manager]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob37E64E52AE5A99C0482579F200203DED</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Underground-Mining-Senior-Project-Manager_1653626.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[The Company Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   The Role They are currently seeking an experienced Project Manager required to manage operations in WAs norhtwest. The ideal candidate will have a well developed understanding of Underground Mining operations and have be able to demonstrate a high level of experience in Project Management, preferably with Contractor organistions. Reporting to the Operations Manager, the Project Managerandrsquo;s role will include acting as the overall Site Manager; ensuring consistent standards are met and be the main point of contact for the client.     The Requirements As the successful candidate, it is essential that you possess the following skills and experience: Tertiary Qualifications Mining Engineering or Management or related areaConsiderable experience in mine management, shotcreting and shaft lining and managing large mulit million dollar projectsPrevious leadership experience over a variety of departments including project control, commercial, ops readiness, HSE, and engineering.A passion for achievement through team building and culture A demonstrated focus and commitment to commercial imperatives and the time critical elements of successful mine operations.    The Rewards The position offers a competitive remuneration of up to and200,000 to and220,000 base salary pa and the work is challenging. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Drilling Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6A95A137E5D5C153482579F20022421B</referencenumber>
<City></City>
<Country><![CDATA[- North America]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/jobs.nsf/v/C153482579F20022421B</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[Engineering degree required.   A minimum of 10 years experience in drilling operations/engineering    Experience with floating drilling operations is required.    Experience planning, developing operational procedures and executing the drilling of high pressure and high temperature wells   Excellent teamwork skills are required and excellent communication/ presentation skills are beneficial.   Must be able to pass and maintain offshore medical and safety training requirements as well as subsea supervisor level well control certification  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Contract</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Rockdump Package Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0644C8F519A10733482579F200248522</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Rockdump-Package-Engineer-073348.html</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[This will include provision of technical input into contract documentation, contractor selection and provision of contract coordination support. Secondary stabilisation includes dredging/ sand backfill with BHDs, CSDs and TSHDs and rockdumping with SDVs and FPVs. An additional responsibility is supporting project wide safety initiatives including development and implementation of an Incident and Injury free (IIF) culture and safety management planning. Assist Subsea and Pipelines Lead Stabilisation Construction Engineer to direct the activities of detail design contractor engineering personnel during Phases 4. Actively direct contractors and vendors to ensure methodologies and documentation are of consistently high quality and meet corporate requirements. Support the effective interface between design and construction teams and between Upstream and Downstream teams. Ensure the delivery of quality engineering/construction documents to meet the construction schedule. Maintain positive and effective working relationship with other upstream engineers / coordinators and project work teams and contractors.  Requirements Tertiary education preferred - not mandatory. Recognised Civil Engineering qualification. 10 Years minimum in marine construction engineering and management with at least 6 years experience in dredging and rockdumping including oil / gas pipelines. In depth knowledge of marine construction equipment and methodologies related to pipeline trenching and secondary stabilisation and in particular associated with oil and gas activities. The candidate should have specific experience in the design and execution aspects of nearshore and offshore secondary stabilisation of large diameter trunklines including dredging/trenching with BHD and CSD equipment and rockdumping with SDV and FPV equipment. Marine works coordination and site supervision is also required for the execute phase.  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Not Specified</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Structural Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob93BCB850C9BC93BB482579F20022BA0D</referencenumber>
<City><![CDATA[Houston]]></City>
<Country><![CDATA[- North America]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/jobs.nsf/v/93BB482579F20022BA0D</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[Job Description  Review Contractors structural engineering deliverables and ensure quality is consistent with Company requirements  Review and ensure that Company structural specifications are incorporated into project specifications and applied throughout the engineering design  Review Contractor procurement packages for structural components  Respond to Contractor technical queries regarding structural issues  Monitor and report on Contractor structural engineering progress  Interface with other disciplines within the Company Project team in Contractors office on all aspects of the work  Requirements Required Skills and Experience  10-20 years of experience in the offshore oil and gas industry  Strong technical and analytical skills  Expertise in the structural design of decks or modules for offshore platforms  Demonstrated teamwork, leadership and communication skills  Preferred Skills and Experiences  Experience working as a client representative for a major oil and gas firm  Post-graduate degree in Structural engineering or similar engineering degree  Proficiency in structural analysis software, such as SACS, and finite element analysis software, such as Ansys or Abaqus.  Experience with specialty analysis, such as transportation and seismic.  Experience with fabrication and construction support.  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Contract</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Commissioning Planner]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA68D02736C3017E7482579F2002C4157</referencenumber>
<City></City>
<Country><![CDATA[- Europe]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Commissioning-Planner--17E748.html</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[Reports to: Commissioning Manager   Responsible for developing and updating Level 4 Commissioning Schedule   Liaison with Project Planning group ensuring alignment/ integration of level 4 commissioning schedule with project EPC schedule   Ensure alignment with project schedules and planning teams   Develop and implement the work process for effective planning of pre-commissioning/ commissioning activities;   Develop tracking progress reporting systems for commissioning execution schedule;   Establish tracking/ reporting linkage where required with other project tools and reporting such as Turnover System Tracking Reporting;   Responsible for ensuring that all commissioning activities are executed per the schedule, and that all documentation is compiled ensuring that they will be available as part of the Project Turnover Documentation;  Produce monthly reports of current status and issues relative to pre-commissioning and commissioning plan and ongoing activities.   Requirements LNG facility pre-commissioning and commissioning planning LNG EPC pre-commissioning/ commissioning planning past exposure  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Not Specified</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Engineering Process Manager]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA95BED3D35B02606482579F200297319</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineerjob.us/jobs.nsf/v/2606482579F200297319</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[Requirements Bachelor Degree in Engineering Min 10-15 years Owner/Operator experience Alberta Oil Sands Major Projects experience is an asset Extensive hands-on Maintenance Management, Asset Management experience working on live operating facilities Full project lifecycle  Familiar with the development, implementation and management of Maintenance and Reliability programs and systems (eg ERP, SAP), including spare parts Familiar with Maintenance Best Practices and Operational Excellence Demonstrated experience in developing, writing, implementing maintenance related EM standards, procedures, specifications, work practices, processes Excellent communications skills, including writing  Ability to work both independently and as part of a team Practical, hands-on, focused Proficient in Microsoft Office, specifically Excel, Word, PowerPoint and Visio Excellent analytical, interpretive and computer skills Excellent interpersonal and communication skills Strong relationship-building, facilitation and negotiation skills Must be able to understand and assess diverse stakeholder interests and drive towards practical, shared solutions Must be able to manage competing priorities and demonstrate superior organization skills Independent, self starter able to initiate and recommend solutions encompassing various technical specialties  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Not Specified</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HSE Manager  Iron Ore Developer  Perth Based Role  African Project]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 30 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAEC1A1ADFE4DFF47482579F200340C42</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/HSE-Manager-Iron-Ore-Developer-Perth-Based-Role-African-Project_1653725.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Our client is currently moving into the construction phase of a large scale Iron Ore development in Africa.    They are currently looking to bring on a corporate HSE manager to develop and implement all Health, Safety and Environmental procedures.    Reporting to the COO you will be based in Perth overseeing the successful implementation through a number of HSE officers on the ground in Africa. You will be responsible for all operational and exploration project sites.     Major Responsibilities:          Develop and implement HSE strategies Oversee all procedures and constantly improve and develop existing policies. Identify any risks and develop assessments and strategies to minimise the risks. Ensure all local HSE legislation is adhered to. Develop annual HSE training programs and oversee this.  Conduct HSE training as required, ensuring work groups are engaged and actively participating in the support of hazard reduction. Accident assessment and investigation. Mentor site based HSE officers. Oversee project teams throughout construction to insure procedures are being followed. The review of contractor HSE Management Plans for adequacy and compliance to company standards. Stand at the forefront for the company for all HSE issues.  Requirements:    Relevant qualifications in HSE. 15 years plus experience with the last 5 years at a corporate or group level. Must have had experience working in Africa on a greenfield construction of an open cut mine. Professional member of Institute of Occupational Safety andamp; Health or equivalent. Computer literate with extensive knowledge of Microsoft Office Suite. Experience working in hardship locations with a mix of different cultures. Able to travel frequently to site.  Our client is looking for a true professional who is passionate about heath, Safety and Environment issues.     You will need to adapt to different environments under difficult working conditions in Africa. If you are looking for a challenging and rewarding role, coming in at the ground level, this is for you.    There is a generous package and career development on offer for the right candidate.    For a confidential discussion, please send your CV to Glenn Shields in ACRWORLDs Mining Division for review. (Preferably as a word document attachment)     View hundreds of job opportunities on our website www.acrworld.com  Follow us on twitter        www.twitter.com/acrworld  Follow us on linkedin      http://www.linkedin.com/companies/acrworld-international-search]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Subsea Flowlines Installation QA Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 02 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFE564C954899EC3F482579F2002E8C65</referencenumber>
<City></City>
<Country><![CDATA[- Europe]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Subsea-Flowlines-Installation-QA-Engineer--EC3F48.html</url>
<company><![CDATA[Integrated Resources Management Pte Ltd]]></company>
<description><![CDATA[Define and support Project Management in the development and implementation of Project Quality Management System identifying the appropriate processes and procedures and supporting requirements. Reinforce the HSSE requirements to the contractors and second party inspectors. Develop and execute a Project Quality Plan appropriate for the Project phase. Monitor and measure effectiveness of the Quality Plan. Work with the Project Team to promote the right Quality mind-set and behavior requirements for successful project development and implement. Develop general Quality Resource organizational plans and budgets. Support Project Team to ensure that the Project deliverables meet quality targets defined by the Project. Compile and submit Project Quality Dash Board to Project.  Provide guidance on any specific requirements that may be needed the Project may interface with third parties, or customers that utilize ISO 9000 Quality Management Standards. Participate in the development of Contact QA requirements and selection / evaluation process. Support developing and successful implementation of the Project Assurance Plan (PAP) and the Technical Assurance Plan (TAP).  Requirements Over 15 years of experience applying the discipline skill to oil and gas equipment / construction and 10 years of experience as Quality or Project Engineer. (JG3). Able to perform, comply, audit and make assessments of Safety Management System (Advance Safety Auditing, Behavior Safety System, JSAs, act) and have competency in safety procedures.  Able to interface with other disciplines at the various stages Familiar with DEP specifications.  ]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Not Specified</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regional Operations Manager  Underground Mining]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5A0115CEBC0F2FD5482579F2003AD5BB</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Regional-Operations-Manager-Underground-Mining_1653763.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian contracting group operating in the areas of Mining and Civil Construction. With offices throughout Australasia, they employ thousands of people to work on major projects and they have a reputation of delivering high standards of work and innovative solutions.   They are currently seeking an Operations Manager with experience in the Underground Mining industry. Based either at the head office in Brisbane or Perth, you will be required manage and oversee the underground mining operations on the East Coast.   Reporting to the General Manager of Underground, your primary responsibility will be to oversee the satisfactory performance of various core function support and service areas and to oversee the safety, quality, schedule and budget performance of the underground projects group. Your responsibilities will include; Providing operational support to the Project TeamsReviewing all Financial and Progress reportsReviewing scopes of workLiaise with all internal and external stakeholders to ensure strong relationships with the team and with the clientEnsure that all Project Management Plans are followedEnsure that Contract Conditions are met to the clients satisfactionReport to the Corporate Management Team quarterly analysis on performanceProduce and manage action plans for the divisionLiaise with immediate Administration teamBuild company profileEnsure tenders are evaluated and responded to in a timely and professional manner  Your experience within the Underground Mining Industry will be highly regarded and candidates will be required to have a Mining andamp; Engineering background. A minimum of 10 years industry experience is required. There will a number of direct reports so it is essential that you have good people skills, an effective management style and excellent communication abilities. A well-developed commercial acumen is also very important. The position offers a competitive remuneration package, challenging work and excellent career development. There is the opportunity to be part of an enthusiastic, dynamic, approachable and friendly team with future prospects within a well reputed organisation. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pipeline Engineer  Onshore Oil and Gas]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE16ACDBEED61BEF4482579F2003AD5F3</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Pipeline-Engineer-Onshore-Oil-and-Gas_1653764.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Engineering, Construction, Building and Maintenance company with a global presence. Their expertise is based on complex infrastructure projects in mining, oil and gas, power, and public infrastructure. Due to current project requirements they are seeking experienced Cross Country Pipeline Engineers who have experience working on pipeline  construction projects. The project will travel throughout central and northern Queensland and is expected to take a couple of years to complete. This is a chance to work on Australias longest and largest diameter pipeline. Employees will be flown to site for a 28 day on and 9 day off roster, meals are provided and each employee will be living in demountable accommodation with a single room and bathroom. Ideal candidates will have previous experience working on onshore pipeline construction projects preferably within the Oil and Gas sector. Strong communication skills are essential as you will be required to liaise with clients and sub-contractors on site.In order to be successful, candidates will be required to display;   Minimum of 5 years experience in a Project Engineering or Site Engineering roleExcellent communication skills, both written and verbal;Experience working with project progress reports to management;A good commercial acumen;Tertiary Qualification in Engineering - Bachelors of Civil/Structural Engineering Preferred;Australian experience  This is a long term, staff position based on the project site between Dalby and Gladstone. Candidates will be required to work a 28 day on 9 day off Fly-In, Fly-Out roster. If you are interested in working on an exciting and revolutionary Oil and Gas project, then apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Estimating Manager  Commerical Construction]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob75F99012D49B843D482579F2003AD615</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Estimating-Manager-Commerical-Construction_1653980.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is a West Australian Developer and Builder that has been creating highly successful property developments, land subdivision and construction projects for many years. They have a Group of Companies that, with combined capabilities, provide an unparalleled resource for property development. Due to a substantial Company restructure, our client is currently seeking an experienced Estimating manager to assist in driving the Company in the right direction and maintaining a high level of service to the Building and Construction industry. We are looking for someone with experience in Estimating within the Building environment, who is familiar with risks related to the building industry and who has experience with residential and building projects. Reporting to the CEO, the responsibilities of the Estimating manager will include (but is not limited to); Tender Management Manage a team of Estimators across a Group of CompaniesInterfacing with the front end of the business including Engineering and ProcurementReview specification and drawings to complete bid review formsPerform bid evaluationsPrepare concept layouts for estimating take offsReviewing all estimates prior to submissionProvide pricing in a timely mannerFollow up tender results and update tender registerDevelop and maintain client relationshipsWe are looking for a candidate who has a high level of initiative and andlsquo;get up and goandrsquo;. You must be an excellent communicator and Australian experience is essential. You will be rewarded with a long term career, a competitive remuneration and potential career advancement as the company continues to grow.      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Process  Flow Assurance Engineer]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4A943CE2656AF337482579F2003AD677</referencenumber>
<City><![CDATA[PERTH]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Process-Flow-Assurance-Engineer_1654023.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is one of the worldandrsquo;s leading engineering and design consultancies with global operations.   They provide high-end Design and Project Engineering, Assurance and Consultancy to the oil and gas upstream, midstream and downstream environments and a range of applications including fixed and floating offshore structures, terminals, refineries, petrochemical plants and pipelines.  Our client strives for excellence by recruiting the best and harnessing the skills of their people, investing in their career progression and continued development. Flow Assurance refers to the successful and economical flow of hydrocarbon stream from reservoir to point of sale. Process Engineering focuses on the design, operation and control of that said process. Due to expansion, our client is in immediate need of an experienced Process Design, Flow Assurance Engineer to complement the team by adding value and expertise. As a senior member of the team you will use your excellent communication skills and work closely and effectively with the other disciplines always ensuring a high quality standard is maintained throughout. With this, the responsibility of input to estimates, proposals and production of design deliverables will be yours to deliver on time in full providing expert advice and assistance to design and operations. You will be contributing to business development activity including meetings and tenders keeping abreast of changes to relevant technology and design tools. Your involvement will also include fluid sampling protocols and testing, fluid characterisation reports and quality control. To be successful in the role the following will be a requirement; Degree in Chemical Engineering or Science degree with specialisation in fluid dynamics.Hands-on transient thermal-hydraulic modelling/simulation work in the support of the design and operation of offshore facilities including: wells, pipelines, risers, separations and pressure-boosting equipment using OLGA is essential. Solid OLGA experience on multiple projects is a must.Hands on steady state modelling experience using PIPESIM and HYSYS is essential.Demonstrated process design experience is essential. Experience in the oil and gas industry within the multidiscipline design environment.Experience with fluid characterisation and liquid surge analysis is highly desirable. You will be presented with opportunities and new challenges along with competitive remuneration and flexible leave arrangements. If you are interested in joining this well-known market leader that is committed to helping its employees reach their potential then apply now.      ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Project  Package Engineer  Oil & Gas]]></title>
<date>Wed, 02 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 27 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE30B9C0F2B05E9FD482579F2003AD6B6</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.engineeringjobs.net.au/job/Mechanical-Project-Package-Engineer-Oil-and-amp-Gas_1654035.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client provides engineering design and implementation solutions for the oil, gas and chemical industries internationally. From concept to operation, they are involved with engineering, design, drafting, and project management. Due to an increase in workload, they are seeking a Mechanical Project Engineer to be based at their Brisbane office. This is a long-term position involving Project Engineering and Package Engineering responsibilities with a reputable Oil and Gas Engineering firm. We are looking for candidates who have an understanding of; Filter vesselsSlug catcherFlow Control  skidsPiping FabricationThe Package Engineer will also be required to oversee valves supply andndash; actuated ball, plug, flow control, and anti surge.   Responsibilities should also include, but will not be limited to; Taking part in Hazops;Performing reviews;Ensuring safety standards are adhered to;Site inspection;Producing commissioning plans andamp; procedures.In order to be successful, candidates must demonstrate Mechanical Engineering Degree5+ years experience as a Project Engineer or Package Engineer in the Oil and Gas industryProject Engineering ExperienceStrong leadership qualities and paramount communication skills are a must for this role as it is an interface role. Australian Experience is required. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SQLJavaHTML programmer  Netherlands]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 31 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF2994263599FF5EA482579F30000601B</referencenumber>
<City><![CDATA[Amsterdam]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SQL-Java-HTML-programmer-Netherlands_1655824.html</url>
<company><![CDATA[Lawrence Harvey Search and Selection]]></company>
<description><![CDATA[SQL/Java/HTML programmer - Netherlands  On behalf of our prestigious client in the financial sector, we are currently looking for a SQL programmer to help building a load validation tool for a compliancy program.  With the help on business consultant the SQL programmer will make sure the data entered in the system are validated and according to the standards agreed with the business. Also, the consultant will have some web presentation skills (Java and HTML5).  The home made  web tool will  allow various  datasets in the  SQL Server database to be loaded. The tool will ensure that the right data is uploaded and provide validation, authorization, and 4-eye principle.  - Deliverables - Dependencies on other projects - Web application that demands specific function to load Excel files to be validated and uploaded to the database - Hay-scale job profile  Asset management processes understanding a plus.  If you have the required skills and interested, please send your CV now for immediate consideration.  Lawrence Harvey is acting as an Employment Business in regards to this position.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Senior Drilling Engineer]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 31 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob75AE618B02BDAE26482579F300006110</referencenumber>
<City><![CDATA[Adelaide]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Drilling-Engineer_1658295.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[ A global energy services company, who pride themselves on technical excellence, is looking for an experienced Drilling Operations Engineer to join their team in Adelaide. Your role will play an integral part in helping them become a respected and admired supplier of energy in the world.With big plans for expansion this consultancy is looking for a Senior Drilling Engineer to look after an unconventional drilling rig.  Your main responsibilities will include the supervision of drilling operations, well planning, provision of engineering support and cost estimates. This is an office based role with on call weekend shifts required on rotation.To be successful in this role you will need to have a minimum Bachelor of Engineering in the relevant area (e.g. Civil, Petroleum Engineering), considerable Drilling Operations Experience is crucial. In addition candidates must be able to demonstrate excellent written and verbal communication skills. Hays Globalink is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the TandCs, Privacy Policy and Disclaimers which can be found at hays.co.uk]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Principal Electrical Engineer]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2479F2A1976A2462482579F300188F10</referencenumber>
<City><![CDATA[Adelaide]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[South Australia]]></State>
<url>http://www.expatengineer.net/job/Principal-Electrical-Engineer_1660084.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services. Due to growth, development and project demands, they are currently seeking a Principle Electrical Engineer. To be considered for this role you must demonstrate the following: Degree in Engineering in relevant Discipline, or equivalentMinimum 12 years engineering experienceExtensive technical, practical and leadership experience in the relevant discipline in the same or similar industryHSEC FocusedSelf MotivatedLeadership skills andamp; Team OrientatedDisciplined andamp; Results DriveAustralian working rights and experience In this role you will be responsible for managing a team of electrical engineers across a range of projects in the mining industry. Drawing upon your technical and management skills, you will be overseeing the smooth running of electrical projects. Our client is a reputable EPCM engineering firm so this is an excellent career oppotunity in a growing industry. If this sounds like you please send your application ASAP!     ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Control Systems Engineer  Mining & Resources]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE1B181815A8C614482579F300188F2F</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Lead-Control-Systems-Engineer-Mining-and-amp-Resources_1660085.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in West Perth. The ideal candidate for this role will be someone who has a minimum of 7 years experience as a Controls Systems Engineer.  The role of the Lead Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportMinimum of 5 years industry experience in the Australian market Candidates will be required to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Provision of technical guidance to junior engineers and peers;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts.    The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; SCADAElectrical engineering including designProject engineering activities    We will be looking for candidates who have experience in Control Systems Engineering within the Mining andamp; Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Assistant  Engineering]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob57381534C961E7AC482579F300188F51</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Technical-Assistant-Engineering_1660086.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Assistant to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsHelp with proposalsAssist with invoicingAssist with writing technical dcuments and manualsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleA relevant qualification would be advantageousExcellent MS office skillsTechnical/Electrical drafting backgroundGood organisational and administrative skillsBe a team playerEnjoy a busy work environment If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer  Hazardous Area]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8AFB74095BEFBC20482579F300188F70</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Electrical-Engineer-Hazardous-Area_1660087.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking highly experienced Electrical Engineers from the Oil andamp; Gas and Hydrocarbon industries, who have a strong knowledge of the Hazardous Area. Opportunities exist in both Perth and Brisbane.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and GasDegree or equivalent experience/qualificationsExperienced with Hazardous Area Technical writing and design specification experience Experienced with High Voltage     The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.Produce electrical designs as required.In addition produce instrumentation and control systems designs as required.Carry out electrical testing and associated electrical installation works as required:In accordance with the relevant legislation, andWithin the employees competencyAs authorised by the Employer, andSo as to meet project requirements    We are looking for candidates who are able to display at least 5 years experience in Electrical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! Australian experience is necessary!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Control Systems Engineer  Mining in Mackay]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob935B66768E8715B8482579F300188F9A</referencenumber>
<City><![CDATA[Mackay]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Control-Systems-Engineer-Mining-in-Mackay_1660088.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Control Systems Engineer to join the team in Mackay. The ideal candidate for this role will be someone who has a reliable level of experience in design and project management within the mining and resource industry. You should now be at a level where your management skills are well developed, or you are now ready to expand into this responsibility.     The role of the Control Systems Engineer will be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.  The successful applicant will ideally possess: Bachelor of Engineering (Electrical) High end computer literacy Well developed written and verbal communication skills Site Commissioning experienceProven record in site supportExpereince working in Regional Areas5 years industry experience in the Australian market The successful applicant will also have Proven Technical skills in: Control Systems EngineeringSoftware engineering including specification writingPLC andamp; OIS programming and testingElectrical engineering including designProject management activities    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away!       ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer  Control Systems in Mining & Minerals]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob59528BF7B33EAB41482579F300188FC4</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.expatengineer.net/job/Project-Engineer-Control-Systems-in-Mining-and-amp-Minerals_1660089.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth and development, they are currently looking for an experienced Project Engineer to join their team in West Perth. Candidates are required to have had some experience in the Mining and Minerals industry and you will be required to provide technical deliverables of a project using your background in Control Systems Engineering.     The successful applicant will also have Proven Technical skills in: Control Systems EngineeringPLC andamp; OIS programming and testingElectrical engineering including designProject management activitiesDiscussions with various stakeholders (site operational people to extract information)Project Engineering through implementation phases of the projectTechnical / Report Writing    You will also be required to assist in the control and monitoring of schedules and financial aspects of a project with the team in liaison with the Project Manager.     We are looking for candidates who are able to display at least 5 years experience in a project engineering role and mining industry experience will be highly regarded.     The role of the Control Systems Engineer will also be to engage with Senior Management and the Engineers, providing support and accountability for the delivery of the instrumentation and control system engineering quality within the company.     The successful applicant will ideally possess: Bachelor of Engineering (Electrical)High end computer literacyWell developed written and verbal communication skillsSite Commissioning experienceProven record in site support5 years industry experience in the Australian market    We will be looking for candidates who have experience in Control Systems Engineering within the Resource industry. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal & Lead Process Engineers  Mining & Minerals]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob51549C2D0B4342B6482579F300188FEA</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[South Australia]]></State>
<url>http://www.expatengineer.net/job/Principal-and-amp-Lead-Process-Engineers-Mining-and-amp-Minerals_1660090.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking to engage a Principal and Lead Process Engineers , to become part of the team that coordinates the technical development and assist the commercial team in the development of Greenfield and Brownfield projects through pre-feasibility / feasibility studies. This is a permanent, full time role in Adelaide.     Our client is seeking personnel at various levels of their engineering degrees.     The Person  The successful candidate will ideally have the following qualifications and experience:     Bachelor of Engineering A minimum of 10 years experience as a Process Engineer Mining andamp; Hydrocarbons industry experience Pre-feasibility/Feasibility study work.     Your responsibilities may also include, but will not be limited to; Support of and compliance with HSEC systems ;Acknowledgement and compliance with the companys goals, mission statement and values;Generation of innovative, fit for purpose and cost effective solutions for customers;Recommendation of improvements to engineering systems and processes;Identification of personal development activities to support skills progression; andContinuous development of industry networks and contacts; andFor the more senior candidates; a provision of technical guidance to junior engineers and peers.       We are looking for candidates who have a well developed understanding of the Mining and Mineral Processing industry.  If this sounds like you then please apply now!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electrical Engineers   Hazardous Area]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob726B185AB20EC05B482579F300189012</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Senior-Electrical-Engineers-Hazardous-Area_1660091.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[    Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.     Due to growth, development and on-going work, they are currently seeking highly experienced Electrical Engineers from the Oil andamp; Gas and Hydrocarbon industries, who have a strong knowledge of the Hazardous Area. Opportunities exist in both Perth and Brisbane.  We are looking for candidates who have demonstrable skills in design engineering and project management, and who are able to display; Experience in Oil and GasDegree or equivalent experience/qualificationsExperienced with Hazardous Area Technical writing and design specification experience Experienced with High Voltage     The successful candidate will be required to; Assist in the development and application of engineering and design standards, systems and processes with particular emphasis on performance improvement and compliance / adherence to procedures.Ensure tasks are fit for purpose and are completed successfully (accurately, in a timely fashion and cost effectively).Provide design assistance in the identification, selection and procurement of equipment or components.Participate in review of design before implementation to ensure quality, consistency, and coordination with all aspects of the installation.May act as a Project Engineer or Project Manager when required.Develop and maintain mutually beneficial relationships with key suppliers, keeping abreast of new technological developments.Produce electrical designs as required.In addition produce instrumentation and control systems designs as required.Carry out electrical testing and associated electrical installation works as required:In accordance with the relevant legislation, and Within the employees competencyAs authorised by the Employer, andSo as to meet project requirements    We are looking for candidates who are able to display at least 5 years experience in Electrical Engineering and who are keen to take on andlsquo;SENIORandrsquo; responsibilities. You will need to have well developed management skills, an ability to engage with clients and have a strong technical background. If this sounds like you then please send your details right away! Australian experience is necessary!   ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Field Engineer  mining]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBF69ACD09B4767C5482579F30018903C</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.expatengineer.net/job/Mechanical-Field-Engineer-mining_1660092.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking an experienced Mechanical Field Engineer for this FIFO role.  We are looking for candidate who are able to display; Maintenenace/reliability engineering experience essentialExperience in mining andndash; preferably iron oreDegree qualified preferredBrownfields experienceProject experienceAt least 3 years engineering experienceFull Australian working rightsWilling to do FIFO This is a fantastic opportunity for someone to develop their field experience working with major clients. The role is FIFO but the roster is flexible. Our client is a highly respected, rapidly growing engineering firm and this is your chance to further your career. If this sounds like you, we welcome your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Electrical Designer]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD6D768C79FBA67CD482579F30018905A</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.expatengineer.net/job/Lead-Electrical-Designer_1660093.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking an experienced Lead Electrical Designers to join the Brisbane team. Drafting diploma or equivalent, specialising in ElectricalAdvanced knowledge of Australian Design Codes and Standards. Intermediate knowledge of MS Excel and Word. 15+ yearsandrsquo; experience in Electrical design drafting within an industrial environment. Brownfield/Greenfield Project Experience.Mining/Hydrocarbons experience EssentialProven experience in similar role    The company is actively expanding and is seeking applicants for the role of Lead Electrical Designer based in the Brisbane office. Full time, contract or casual employment arrangements will be considered for this role. Donandrsquo;t miss this excellent opportunity, please send your application through now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Officer  Electrical drafting]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5B508C45FE37939C482579F300189086</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.expatengineer.net/job/Technical-Officer-Electrical-drafting_1660094.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth and development, they are currently seeking a Technical Officer, with an electrical background to join the team in Perth:  In this role you will be responsible for but not limited to: Assisting the engineersClient, customer and vendor interactionAssisting with technical (electrical) drawingsAssist engineers with design of HV/LV plant.Assist in the development of technical documents, specifications and manualsHelp with proposalsGeneral administration To be considered for this role you must display the following: Relevant experience in a similar roleDiploma in Engineering or Electrical Licence is desirable.Experience in power distribution and drives (LV/HV).Development and review of electrical design deliverables (SLDandrsquo;s / schematics / GAandrsquo;s / schedules).Exposure to an industrial engineering environment or office.Exposure to electrical drafting.Experience in electrical design and drawings. If this sounds like you please send your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Manufacturing/Operations</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CivilStructural Engineering Manager]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD013982DBECFAF45482579F3001890B3</referencenumber>
<City><![CDATA[Brisbane]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Queensland]]></State>
<url>http://www.engineeringjobs.net.au/job/Civil-Structural-Engineering-Manager_1660095.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[? Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons and other industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations.  They are currently seeking an experienced Manager who can head the Civil / Structural division within the business, as well as provide technical assistance to the team and engage in business development activities. Preferred candidates will be experienced in the full range of feasibility studies, detailed design and construction.  The responsibilities of the Civil / Structural Manager include, but not be limited to: Manage a Civil / Structural Engineering team in the preparation of feasibility studies, preliminary and detailed designs, and construction.Ensuring all Civil andamp; Structural engineering work complies with statutory and regulatory requirements and company policies and practices.Providing high level technical support for all Civil and Structural engineering work as required.Supervising preparation of documentation for standards, procedures, safe working practices and monitoring regimes in respect of work on or around electrical and instrumentation equipment.Oversee, mentor and develop junior and intermediate Civil and Structural engineers.Perform regular competency assessments of staff team members, develop training and development plans. In order to be successful, candidates will need to have: Professional Degree in Civil or Structural Engineering.Minimum of 15 years experience in the heavy industry, preferably in the mining and hydrocarbons sector.Well-developed management skills and commercial acumen.Excellent communication skills.Excellent people skillsStrong time-management skillsStrong Business Development skills. We are looking for candidates who have well developed management skills, a strong network within Australia and high level of experience within the resource industry.  If this sounds like you then please apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Field Engineer  mining]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFC5060687D13F68C482579F3001890F7</referencenumber>
<City></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.expatengineer.net/job/Mechanical-Field-Engineer-mining_1660173.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[ Our client is a leading Australian engineering and project delivery company operating primarily in the Mining and Minerals, Hydrocarbons, Infrastructure and Specialist industries. They offer solutions for Brownfield and Greenfield projects from conceptual design to operations, and asset management and completion services.  Due to growth, development and on-going work, they are currently seeking an experienced Mechanical Field Engineer for this FIFO role.  We are looking for candidate who are able to display; Maintenenace/reliability engineering experience essentialExperience in mining andndash; preferably iron oreDegree qualified preferredBrownfields experienceProject experienceAt least 3 years engineering experienceFull Australian working rightsWilling to do FIFO This is a fantastic opportunity for someone to develop their field experience working with major clients. The role is FIFO but the roster is flexible. Our client is a highly respected, rapidly growing engineering firm and this is your chance to further your career. If this sounds like you, we welcome your application! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Site Supervisor  Northwest]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB42518FB5504CFF9482579F300189115</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Site-Supervisor-Northwest_1660174.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is a leading West Australian construction and property company operating throughout regional WA for more than 30 years. They have won many awards including Master Builders Awards for Excellence in Construction and their standards are high because they engage people who share their passion for excellence.   Due to growth and expansion they are seeking an experienced Site Supervisor join the team in the Northwest on a 2-3 month contract arrangement, with an opportunity for long term employment for the right candidate.   We are looking for a Site Supervisor who has at least 5 years experience supervising and delivering residential building and construction projects, in particular in regional Western Australia. Previous defect and remedial works experience will be highly regarded.   This position will include managing a team of tradespeople and subcontractors working on projects in the Northwest.   It is expected that candidates have; Experience with residential building and construction projectsFamiliarity with OHS Excellent communication skillsBe able to work to timelines and budgetsExperience working on regional projects (preferred but not essential)  In addition, you will have a strong desire to succeed, you will need to be able to think on your feet, work well autonomously and demonstrate a commitment to quality, high standards and attention to detail.   The role is for an immediate start. Our client is happy to consider candidates who are either residential in Karratha, or Perth based employees on a rotation of 3 weeks on 1 week off.   If this sounds like you than apply now! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Development & Subdivisions Engineer Coordinator]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 03 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob762C3DC33E9D7BF8482579F30026CAE9</referencenumber>
<City><![CDATA[Other Wagga Wagga]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[NSW]]></State>
<url>http://www.engineeringjobs.net.au/job/Development---Subdivisions-Engineer-Coordinator-7BF848.html</url>
<company><![CDATA[Wagga Wagga City Council]]></company>
<description><![CDATA[Development and Subdivisions Engineer Coordinator  Wagga is definitely an advance on the way you live and work.Experienced in Subdivision Development and Construction?Looking for the right change?  Council is seeking a motivated professional with experience in assessing and overseeing a range of development applications, conducting subdivision-related inspections, and in providing engineering expertise to both internal and external stakeholders.  A move to Wagga Wagga is one which is not only to a better lifestyle, but to a vital and different work environment. Want to be valued for your expertise and contributions? This is your opportunity to join a supportive team working with a new leadership focus. This is a critical role for us and we are eager to help you make this a valuable move for your lifestyle and career. This is the change you are looking for.  Come, visit and talk with us. Explore the family options and the diverse projects that you can be a part of.  Position Number: (SCS144)  Salary Range: and80,613and96,700 gpa + super + leaseback vehicle.  Contact: Colby Farmer  02 6926 9510 or Colin Fough  02 6926 9542.  Closing Date: Friday, 25 May 2012.]]></description>
<salary></salary>
<education></education> 
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Development & Subdivisions Engineer Coordinator]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 25 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB8D5E779FE235A71482579F30025910B</referencenumber>
<City><![CDATA[Other Wagga Wagga]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[NSW]]></State>
<url>http://www.engineeringjobs.net.au/jobs.nsf/v/5A71482579F30025910B</url>
<company><![CDATA[Leonard Holt Robb]]></company>
<description><![CDATA[Wagga is definitely an advance on the way you live and work.Experienced in Subdivision Development and Construction?Looking for the right change?Council is seeking a motivated professional with experience in assessing and overseeing a range of development applications, conducting subdivision-related inspections, and in providing engineering expertise to both internal and external stakeholders.A move to Wagga Wagga is one which is not only to a better lifestyle, but to a vital and different work environment. Want to be valued for your expertise and contributions? This is your opportunity to join a supportive team working with a new leadership focus. This is a critical role for us and we are eager to help you make this a valuable move for your lifestyle and career. This is the change you are looking for.Come, visit and talk with us. Explore the family options and the diverse projects that you can be a part of.Position Number: (SCS144)Salary Range:and80,613and96,700 gpa + super + leaseback vehicle.Contact: Colby Farmer  02 6926 9510 or Colin Fough  02 6926 9542.Closing Date:Friday, 25 May 2012.]]></description>
<salary></salary>
<education></education> 
<jobtype>Not Specified</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HSE Project Manager - URGENT]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 03 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob17ADEEBF22D68AA7482579F30031F8EC</referencenumber>
<City></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Alberta Fort McMurray]]></State>
<url>http://www.engineerjob.us/job/HSE-Project-Manager---URGENT-8AA748.html</url>
<company><![CDATA[ISS International]]></company>
<description><![CDATA[Were looking for an HSE Project Manager to be involved in Oil sands Project in Fort McMurray, Alberta, Canada Its required either CSO (Construction Safety Officer) certification or NCSO (National Construction Safety Officer) one or CRSP (Canadian Registered Safety Professional) one or equivalent. Its required experiences in HAZOP / SIL Analysis and a previous experience in oil sands projects. ]]></description>
<salary></salary>
<education></education> 
<jobtype>Contract</jobtype>
<category>Energy &amp; Utilities</category>
<experience>20 years</experience>
</job>
<job>
<title><![CDATA[SQL Server DBA]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob39488A010904F729482579F300352942</referencenumber>
<City><![CDATA[AU]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/SQL-Server-DBA_1660167.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Prestigious Australian Brand CBD located Excellent work environment and career progression Prestigious client seek a Database Administrator with highly advanced SQL Server database administration skills.  Required Skills: Provide database support to address database related incidents and alerts. Proactively identify and contribute to continuous improvement for database support services, processes and tools.Participate in projects re database design and build to meet business and operational needs.Review, plan and execute database upgrades and patches to maintain security compliance, software currency, support compliance with vendors and robustness. Required Skills and Experience: Relevant tertiary qualifications and/or more than 3 years experience in SQL Server database management.Highly advanced SQL Server database administration skills in complex medium to large corporate enterprises; including physical database design, database administration, backup, recovery, capacity planning, performance tuning and database housekeeping including database patching, SQL Server Security management, SQL query language, data analysis and database troubleshooting (using SQL Profiler, and other database tracing tools) These skills include experience a combination of SQL Server 2000, 2005, 2008 and 2008 R2.Highly Advanced knowledge of SQL Server clustering technology; Broad experience in virtualised environments, SAN and NAS technology, Reporting services and High availability environment is highly desirable. Demonstrated experience in Disaster Recovery technologies (Log Shipping, database mirroring, clustering, replication, SAN based mirroring, etc). Experience in the full software lifecycle management and license management of database software and tools is highly desirable.Highly Advanced understanding of application-SQL architecture and broad experience in supporting SQL Server RDBMS with OLTP, OLAP, batch, web service and web based for in-house developed and packaged applications.Demonstrated highly developed analysis, investigative and diagnostic skills with ability to resolve very complex or unprecedented database related problems creatively and effectively. Highly advanced skills in environments where quality processes are an integral part of the support process; experienced in ITIL incident, problem and change management. Other Requirements: Strong written/oral communication with the ability to liaise and communicate effectively with internal clients and colleagues, and convey or translate very complex technical information to target audiences; experience in engagement of vendors for third level support.Highly developed organisational skills with a commitment to meeting deadlines, works effectively under pressure and an understanding of project management principles.Demonstrated ability to work in a team environment and contribute significantly towards team goals. Demonstrated motivation, initiative and ability to exercise sound judgement including matters having a major impact both within and beyond the team. Demonstrated ability to cope with pressure and work under broad direction.An understanding of and commitment to the clients aims, objectives and workplace values, together with relevant policies and guidelines including Editorial Policies, Equity andamp; Diversity and OHandamp;S.   To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Steve McDermott on 02 9994 8953, quoting Ref No. JID300.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>IT and Computing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SQL Server DBA]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob68D91E7A98DCD912482579F3003529FB</referencenumber>
<City><![CDATA[AU]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/SQL-Server-DBA_1660398.html</url>
<company><![CDATA[Sigma Resourcing]]></company>
<description><![CDATA[ Prestigious Australian Brand North Shore location Excellent work environment and career progression Prestigious Australian brand seeks an experienced SQL Server DBA to work in an enterprise level environment initially for 3-6 months.  Required Skills: Provide database support to address database related incidents and alerts. Proactively identify and contribute to continuous improvement for database support services, processes and tools.Participate in projects re database design and build to meet business and operational needs.Review, plan and execute database upgrades and patches to maintain security compliance, software currency, support compliance with vendors and robustness. Required Skills and Experience: 5 years experience in SQL Server database management with a focus on SQL, My SQL, JBoss, Apache, IIS6/7/7.5, Wintel Server Experience (2003/2008/R2), Linux, Sharepoint 2007/2010, SQL Reporting Services and SQL Server Integration Services.Advanced SQL Server database administration skills in complex large corporate enterprises; including physical database design, database administration, backup, recovery, capacity planning, performance tuning and database housekeeping including database patching, SQL Server Security management, SQL query language, data analysis and database troubleshooting (using SQL Profiler, and other database tracing tools) These skills include experience a combination of SQL Server 2000, 2005, 2008 and 2008 R2.Highly Advanced knowledge of SQL Server clustering technology; Broad experience in virtualised environments, SAN and NAS technology, Reporting services and High availability environment is highly desirable. Demonstrated experience in Disaster Recovery technologies (Log Shipping, database mirroring, clustering, replication, SAN based mirroring, etc). Experience in the full software lifecycle management and license management of database software and tools is highly desirable.Highly Advanced understanding of application-SQL architecture and broad experience in supporting SQL Server RDBMS with OLTP, OLAP, batch, web service and web based for in-house developed and packaged applications.Demonstrated highly developed analysis, investigative and diagnostic skills with ability to resolve very complex or unprecedented database related problems creatively and effectively. Highly advanced skills in environments where quality processes are an integral part of the support process; experienced in ITIL incident, problem and change management. Other Requirements: Strong written/oral communication with the ability to liaise and communicate effectively with internal clients and colleagues, and convey or translate very complex technical information to target audiences; experience in engagement of vendors for third level support.Highly developed organisational skills with a commitment to meeting deadlines, works effectively under pressure and an understanding of project management principles.Demonstrated ability to work in a team environment and contribute significantly towards team goals. Demonstrated motivation, initiative and ability to exercise sound judgement including matters having a major impact both within and beyond the team. Demonstrated ability to cope with pressure and work under broad direction.An understanding of and commitment to the clients aims, objectives and workplace values, together with relevant policies and guidelines including Editorial Policies, Equity andamp; Diversity and OHandamp;S.   To apply online, please click on the appropriate link below. Alternatively, for a confidential discussion, please contact Steve McDermott on 02 9994 8953, quoting Ref No. JID302.  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>IT and Computing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Consultant Developer Tibco EAI]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 31 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5B4226F1A8617321482579F3003536EE</referencenumber>
<City></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Consultant-Developer-Tibco-EAI_1660413.html</url>
<company><![CDATA[Lawrence Harvey Search and Selection]]></company>
<description><![CDATA[Consultant Developer Tibco EAI  For one of my worldwide client, im currently looking for a TIBCO EAI Developer for a greenfield project.  Tasks:  - Deliver technical Specification. - Realize development and documentation. - Run technical tests. - Training of more junior developer. - Occasional travel to the US.  Travel and Expenses paid.  Skill required:  - Development TIBCO EAI - Knowledge on working in a SAP environment.  English Speaking Project.  Key Skills: Tibco,EAI, Developer, development,technical, tests,architecture, interfaces,English, SAP.Lawrence Harvey is acting as an Employment Business in regards to this position.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>5 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Head of Business Development and Exploration Manager  Perth based]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob78CDE23401CDC8FA482579F30037AE21</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Head-of-Business-Development-and-Exploration-Manager-Perth-based_1660423.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Business Developer, all Exploration activities both regional as well as near mine, and the Corporate Mine Geology function. Based in the Perth CBD you will be reporting directly to the CEO. You will be accountable for the Business Development, all Exploration activities (both regional and near mine), and the Corporate Mine Geology Function. You will manage a technical team which will focus on delivering effective exploration plans, improving and expanding the Groups business through the optimisation of existing operations and identification of new development or acquisition opportunities.   The duties and responsibilities for this role are as follows; Promote safety awareness in the department as well as contributing to the maintenance and review of procedures and work practices,Ensure support and compliance with all rules and regulations, statutory compliance, company policies, and procedures,Contribute to mine geology budgeting processes, including manning levels and drilling requirements,Plan, budget, Implement and manage suitable exploration programs through to pre-feasibility stage ensuring the highest standard of safety and environmental management,Participate in the provision of reports in timely manner with accurate Geological information,Establish and maintain relationships with government agencies, community groups, and other stakeholders including landowners and indigenous groups.To be successful in this role, you must possess the following as a minimum; Must have Tertiary qualifications in Geology or related subjects,Minimum 15 years experience, largely in metal base exploration and mining,Proven and demonstrated experience in leading and supervising a technical team,Operating experience both in open pit and underground environment,Previous experience in project evaluation and financial modelling,Experience in dealing with resources industry corporate matters,Competency in mining software packages (Surpac and Datamine preferred), Microsoft Office, GIS Packages (Mapinfo or ArcView),Demonstrated commitment and support of Company Values and Behaviours.With attractive salary packages and incentives on offer it is an opportunity not to be missed. If this job sounds like its the right one for you then please apply.          ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Exploration and Production</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Business Development and Exploration Manager  Perth based]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB3F91F8560A29945482579F30037AE60</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/Head-of-Business-Development-and-Exploration-Manager-Perth-based_1660424.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Business Developer, all Exploration activities both regional as well as near mine, and the Corporate Mine Geology function. Based in the Perth CBD you will be reporting directly to the CEO. You will be accountable for the Business Development, all Exploration activities (both regional and near mine), and the Corporate Mine Geology Function. You will manage a technical team which will focus on delivering effective exploration plans, improving and expanding the Groups business through the optimisation of existing operations and identification of new development or acquisition opportunities.   The duties and responsibilities for this role are as follows; Promote safety awareness in the department as well as contributing to the maintenance and review of procedures and work practices,Ensure support and compliance with all rules and regulations, statutory compliance, company policies, and procedures,Contribute to mine geology budgeting processes, including manning levels and drilling requirements,Plan, budget, Implement and manage suitable exploration programs through to pre-feasibility stage ensuring the highest standard of safety and environmental management,Participate in the provision of reports in timely manner with accurate Geological information,Establish and maintain relationships with government agencies, community groups, and other stakeholders including landowners and indigenous groups.To be successful in this role, you must possess the following as a minimum; Must have Tertiary qualifications in Geology or related subjects,Minimum 15 years experience, largely in metal base exploration and mining,Proven and demonstrated experience in leading and supervising a technical team,Operating experience both in open pit and underground environment,Previous experience in project evaluation and financial modelling,Experience in dealing with resources industry corporate matters,Competency in mining software packages (Surpac and Datamine preferred), Microsoft Office, GIS Packages (Mapinfo or ArcView),Demonstrated commitment and support of Company Values and Behaviours.With attractive salary packages and incentives on offer it is an opportunity not to be missed. If this job sounds like its the right one for you then please apply.          ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Exploration and Production</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Ventilation Engineer  Underground Mining]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob02471C435B635361482579F30037AE87</referencenumber>
<City><![CDATA[Mt Gordon]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Ventilation-Engineer-Underground-Mining_1660425.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Located in Perth, our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Ventilation Engineer to join the team in their Queensland operations.   Reporting to the Chief Mining Engineer, this role is a permanent Fly-In-Fly-Out position on an 8 days on/6 day off roster. The position requires close liaison with the underground mining contractor and specialist consultants, where required.   The Responsibilities;   Maintain currency with latest ventilation regulations, techniques and methods.Maintain currency with latest mining technology, equipment and regulations.Assist with the Management of all Mining Contractors on site to ensure adherence with contractual agreements and operational requirements.Conduct ventilation surveys of primary and secondary systems and record all results.Prepare, update and distribute all quarterly ventilation plans.Maintain optimum air quality and heat measurements.Achieve budget physical and cost targets for primary and secondary ventilation activities.  The Requirements;   Degree qualifications in Mining EngineeringFive years experience in underground metalliferous mining.One years experience in ventilation engineering in underground metalliferous mining.Sound competency with computer use and Microsoft Office.Commitment to quality, teamwork, innovation, achieving objectives and outcomes.Ability to meet deadlines, Flexible approach to problem solving, priority setting, and time management.Strong interpersonal skills; verbal and written communication skills  If this sounds like a good opportunity for you then please apply now. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Drill & Blast Engineer  Underground Mining]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 28 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4EB2F5A0CD2159F3482579F30037AEBF</referencenumber>
<City><![CDATA[Mt Gordon]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[QLD]]></State>
<url>http://www.expatengineer.net/job/Drill-and-amp-Blast-Engineer-Underground-Mining_1660426.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an Australian based mining company with a focus on copper production and exploration. They hold mining and copper exploration activities in both the Pilbara region WA, as well as the Mount Isa Block in QLD. Due to current expansions and restructuring, our client is currently seeking an experienced Mine Planning Engineer to join their diverse team. Based at their Northern QLD operation, this is a permanent FIFO position on a 86 roster. Reporting to The Production Superintendent you will be required to prepare drill and blast designs as well as to plan and schedule in accordance with the mine requirements. The Responsibilities Provide stope drill and blast designs in a timely manner for stoping blocks,Maintain quality assurance standards and practices by conducting audit checks and inspections of drilling and blasting requirements,Collection, collation and reporting of mine physical data on a daily basis,Update all plans and weekly production schedules and graphs and any other relevant performance monitoring measures on a daily basis,Ensure continuous improvement by liaising with operators and Supervisors for practical plans,Prepare short term production, long hole drilling and development schedules,Data maintenance including cost control and budget,Training and mentoring staff if required.The Requirements Must have tertiary qualifications in Mining EngineeringAt least five years experience in Drill and Blast in Underground Mining environment,Competency with use of Microsoft Office, Surpac and Ring King software,Ability to write and deliver reports, presentations, business correspondence, reviews and other materials,Ability to diagnose issues, establish plans and determine priorities to achieve objectives,Commitment to quality, teamwork, innovation and achieving results,Ability to meet deadlines,Strong interpersonal skills and ability to communicate skills at all levels.  If you are looking for a great opportunity in 2012, then please send your resume! ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Manager  Traction Power Supply  Australia]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 31 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob31D65662C879CEB2482579F3003EDA63</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Design-Manager-Traction-Power-Supply-Australia_1660241.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Complex, high value electrification projectHighly regarded International Transport solutions providerCareer opportunities beyond initial project.This role will suit an experienced design manager with extensive experience in traction power supply, who also has a strong understanding of the interfacing elements within a rail transport system.            Your role as design manager will be to manage the traction power substation and switching design team and the civil engineering design team. You will also    coordinate communication between these two teams. Additionally you will be responsible for coordinating and managing design integration activities with the other elements of the development - signalling andamp; communications , track-work and overhead wiring.      The goal of this traction power supply design managers role is design delivery including independent verification/validation as well as systems assurance.      This project is part of a complex, multi billion dollar transportation development that includes the electrification of more than 100km of track.  Your potential employers are a global transport solutions provider, with expertise in locomotives, rail infrastructure, electrification, communications, control systems and signaling systems.      Please send your CV to Brian Byrne in ACRWORLDs Rail Division for review (Preferably as a word document attachment)      View hundreds of job opportunities on our website www.acrworld.com  Follow us on twitter        www.twitter.com/acrworld  Follow us on linkedin      http://www.linkedin.com/companies/acrworld-international-search]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transportation &amp; Warehousing</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Learning and Development Advisor]]></title>
<date>Thu, 03 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 31 May 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB0370600CB1EDE4482579F3003EDF20</referencenumber>
<City><![CDATA[AUSTRALIA]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Learning-and-Development-Advisor_1660456.html</url>
<company><![CDATA[ACRWorld]]></company>
<description><![CDATA[Long term opportunity to grow with the companyMid tier contractor in building, construction and civilsImportant function with the project services arm of the business   Learning andamp; Development Advisor      Our client is an expanding contractor based in Perth.  They are making good progress, winning more and more work in the resources industry. We are now looking for a Learning andamp; Development Advisor to work across the business.  With some new important additions to the executive team, this company has expanded to work across infrastructure, mining and LNG projects in the booming resources sector.     The role itself will be to coordinate all training and development for our client, your duties may include but not be limited to:       Assisting the HR Manager andamp; Workforce Development to coordinate all training for the staff base.      Consult relevant stakeholders regarding the training needs of all staff and individuals.         Conduct and analyse all data regarding training and development.      Coordinate both internal and external training for employees.      Develop and implement company and individual training plans.      Monitor training budget.      Promote an environmentally conscious culture in accordance with the Environmental Management Framework.       The candidate we want will show strong initiative and demonstrate loyalty to an organisation in Australia.   Ideally the candidate will have experience working for a construction or resources aligned business.    As a reward, the company will have a competitive salary, bonus, along with the opportunity to be part of an exciting phase for a well known company.    They know that every employee has something important to say, and that every employee is integral to the success, appreciation is the best motivation.     It is important to reiterate that the overall projects this company work on are of the highest profile on the global resources platform.       All applications will be treated in strictest confidence - we understand especially in this provision this is paramount.  Any initial questions you may also have, we would be happy to help.  If you are interested, please apply to this advert or send your CV to Tom.Desborough@acrworld.com for review. (Preferably as a word document attachment).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Health Care;Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Murex Developer]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 01 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob86E5CE02EFC034E0482579F3006E91CD</referencenumber>
<City><![CDATA[Hannover]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Murex-Developer_1661002.html</url>
<company><![CDATA[Lawrence Harvey Search and Selection]]></company>
<description><![CDATA[Lawrence Harvey is looking for an experienced Murex MLC developer to join an international company based in Hannover/Germany. The consultant should have at least 3 years experience as Murex developer and must have very solid experience with Murex MLC 1.54 and 1.6. English speaking project, German skills a PLUS. Im looking forward to receiving your application.   Lawrence Harvey is acting as an Employment Business in regards to this position.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Hydrologist Expert]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 01 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8C57B470957284EE482579F3006E9476</referencenumber>
<City></City>
<Country><![CDATA[GHANA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Hydrologist-Expert_1662266.html</url>
<company><![CDATA[EWI Recruitment]]></company>
<description><![CDATA[ A multi-disciplinary Consultancy is seeking a senior Hydrologist professional to work in Ghana. The Hydrologist Expat will demonstrable experience in surface water assessment, modelling and engineering. The successful candidate will have a degree in civil engineering, earth sciences or similar and ideally have a Masters degree in hydrology The successful candidate will join a team of 5 surface water specialists. The purpose of the role will be to expand the capabilities the group and to service the expanding work load. Key Responsibilities The successful candidate will join the water team, working in close collaboration with the team leader on a range of projects. The role will be a predominately technical focused, providing senior level input to a rapidly growing portfolio of surface water related projects in the mining, manufacturing, oil and gas and land development sectors. Although the surface water team service the UK market and are involved in multidisciplinary UK based studies, in particular flood studies; a large proportion of the work delivered by the team is non-UK based. For this reason, the successful candidate will be required to travel, typically for 1-3 weeks at a time throughout the year. A great deal of the current workload is related to Mining projects is sub Saharan Africa, for example: hydraulic design, operational water balances, drainage design, surface water components of ESIA, and dam and spillway design and dam break studies. For more information about this role or other please contact Megan Burges  ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Scheduler  Oil & Gas]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 01 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7FD3CEB327BD8201482579F3006E96E6</referencenumber>
<City><![CDATA[Calgary]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Scheduler-Oil-and-amp-Gas_1664224.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is currently seeks a Project Scheduler to work on a range of large Oil and Gas projects based in Calgary, Canada. Experience of Operations, Turnaround and Shutdowns would be preferred in particular with any experience of oil sands or Shale Gas projects. Responsibilities will including:- coordinate assigned day to day activities and manage scheduling work load with contractors. Build CPM, logically driven construction schedules at various stages of the project life cycle. Specific emphasis is placed on Final Investment Decision (FID) and Issued For Construction (IFC) schedules. Analyze schedule logic, activity durations, constraints, float, resource loading etc. Review critical paths, Level resources as needed to support project constraints. The ability to link detailed engineering and construction schedules with activities to build a complete integrated project schedule. Provide assurance on schedules submitted by contractors according to the project guidelines. The ability to use prior project knowledge to build conceptual schedules is preferred. The ability to develop a schedule risk analysis component of the schedule assurance process. Participate in the interactive planning meetings for projects requesting final investment funding as part of the assurance activity. Understand and use the IPA scheduling metric tool to improve schedule predictability. Incorporate IPA recommendations regarding scheduling into current scheduling process. Help develop, maintain and revise scheduling templates that incorporate all project phases. Help collect and report scheduling information quarterly to support development of the KPI stoplight charts. Perform analysis to track deltas between planned and actual dates and durations. Create a statistical understanding of planned data versus actual outcomes. Assist in progressing construction schedules in accordance with the approved progress measurement strategy. Participate in field walks to validate scope. Help develop and update schedule procedures and work processed as necessary. You will need to have an Engineering Degree or Certification as a Planning / Scheduling Engineer or have equivalent experience. You should be able to demonstrate some industry experience in planning positions. Have good written and oral communication skills. Have good working knowledge of Planning principles and techniques and experience in using Primavera P6. You need to have four to five years experience of working in the Oil and Gas industry. You must be eligible to work in Canada.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>4 Years Experience years</experience>
</job>
<job>
<title><![CDATA[Mining Engineers]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Sat, 04 Aug 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0DDDA1F44F73E56A482579F400270FD0</referencenumber>
<City><![CDATA[Newcastle]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Brisbane and Perth]]></State>
<url>http://www.engineeringjobs.net.au/job/Mining-Engineers-E56A48.html</url>
<company><![CDATA[Maptek]]></company>
<description><![CDATA[Experienced Mining Engineers are invited to apply to join our growing Technical Services teams. In this vibrant environment, your contribution will be valued and your voice heard. You will gain exposure to a variety of mining operations and projects, while working from your chosen office location, such as Newcastle, Brisbane or Perth. Responsibilities include developing and maintaining relationships with Maptek customers and meeting defined business outcomes. The goal is to ensure that customers are getting the most out of our Vulcan 3D modelling and mine planning software.To be successful in this position, you must have working experience in any Mine Planning or Geological Modelling Software. You must possess strong interpersonal, technical, communication and presentation skills. A tertiary qualification in Mining Engineering or equivalent is required. Maptek is the world leader in the development and supply of software and hardware technologies for the mining industry. We deliver solutions across the mining lifecycle, including Maptek Vulcan and Maptek I-Site, as well as highly regarded professional services. We reward our people with a competitive salary, a friendly workplace, flexible hours and job sharing that encourages creativity and individual contributions. Bring your passion, talent and drive to our collaborative and rewarding environment. Please submit your covering letter, resume, salary expectations and preferred location as soon as possible.These positions are for Australian citizens and permanent residents only.]]></description>
<salary></salary>
<education>Degree</education>
<jobtype>Permanent</jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Project Manager  Commercial Construction]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 29 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7793CB4C8C8AFD5E482579F4003FB32A</referencenumber>
<City><![CDATA[Como]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[WA]]></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Project-Manager-Commercial-Construction_1665876.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client is an innovative construction company operating in the commercial and industrial sectors of QLD and WA. They are known for specialising in the completion of prestigious commercial construction projects from design through to hand over, managing all aspects of the commercial construction process.   Due to an increase in workload, our client is now looking for a Project Manager to join their team in Como.   The role and responsibilities of the Project Manager will include, but not be limited to;   Submitting VariationsDocument flow distributionManagement and coordination of subcontract and supplier agreementsMaintaining and managing all incoming and outgoing contractual correspondenceProviding comprehensive support for all contract administration processes with a view to developing a systematic standard for all projectsProvide support in claim management and documentation including variation management, reporting and contract entitlements;Prepare procurement documentation ensuring that suppliers, subcontractors and consultants are fully aware of their obligations for project deliveryReview, as appropriate, non compliance reports which may have an impact on the contractWork with Project Managers to accurately forecast costs and incomeSub-contract documentation preparationManagement of head contractManagement of sub-contracts  The ideal candidate for this role will have previously worked for a commercial building and construction contractor in Australia and holds a degree in Construction Management and Economics.   In order to be successful, candidates will need to display; A degree in Construction Management, Quantity Surveying, Economics or similar or currently studying;Up to 5 years experience in a similar roleHave excellent communication skills, both written and verbal;Good analytical and strategic thinking capabilities;Excellent problem solving abilities;An excellent commercial focus and well developed commercial acumen  This position offers a competitive remuneration package, challenging work and excellent career development. Australian experience essential. If you are ready to join a reputable company south of the river APPLY now!    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[E & I Engineer  Onshore oil and gas]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 29 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2980D2857D68BF7F482579F4003FB34F</referencenumber>
<City><![CDATA[Perth]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Western Australia]]></State>
<url>http://www.engineeringjobs.net.au/job/E-and-amp-I-Engineer-Onshore-oil-and-gas_1665924.html</url>
<company><![CDATA[Energy Human Resources]]></company>
<description><![CDATA[Our client has been designing, drafting and managing projects in the oil, gas and chemical industries for over 16 years. They provide engineering design and implementation solutions for the oil, gas and chemical industries throughout Australia. From concept to operation, they assist with engineering, design, drafting, and project management needs. As part of planned, strategic growth and dedication to current and upcoming projects, our client is now seeking an Electrical andamp; Instrumentation Engineer to join their team in Perth. Reporting to the General Manager, you will be responsible for: Originating and checking documents including block diagrams, hook-up diagrams, termination diagrams, schematics, loops, fire and gas layouts, instrument layouts, cause and effects and Pandamp;IDandrsquo;sHazardous areas for metering, gas compression, fire and gas control and safety instrumented systemsConceptual, FEED, detailed design, construction, commissioning and maintenance phases  Your skills and knowledge include: Electrical andamp; Instrumentation Engineering Degree or equivalent5 andndash; 7 years relevant industry experience in onshore oil and gas preferrablySound experience in electrical and instrumentation design is essentialGeneral understanding of Pandamp;IDsExposure to PLCs and SCADA systemsAbility to produce datasheets and general Eandamp;I specificationsGood understanding of Australian codes and standardsProven ability to liaise with ClientsPrevious experience in controlling small to medium sized projects    Our client offers an attractive salary package, a friendly, flexible and professional working environment and the opportunity to be part of an innovative and expanding global organisation, working with some of the best in their field.  If youandrsquo;re interested in joining a growing company with an attractive salary package then apply now.    ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Live Line Mechanic]]></title>
<date>Fri, 04 May 2012 00:00:00 GMT</date>
<Closedate>Fri, 01 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCE30831421F22149482579F4004A80CC</referencenumber>
<City><![CDATA[NEW ZEALAND]]></City>
<Country><![CDATA[NEW ZEALAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Live-Line-Mechanic_1665878.html</url>
<company><![CDATA[Hays]]></company>
<description><![CDATA[Working on Distribution LinesGreat company with depot in Christchurch and Palmerston NorthOpportunity for a career upgreat in the futureOur client is a well respected company and is known for their excellent service in the power distribution industry.   While launching a new depot this is your chance to work as a Line specialists based on the Christchurch or Palmerston North distribution lines.   You will be responsible for the conductor preparation and stringing, pole preparation and erection as well as conductor replacement andamp; repair.  The successful applicant will have overhead power lines construction experience and a relevant Line Mechanic licence.   In return you will be offered a highly competitive salary, ongoing training and development as well as a great lifestyle and work life balance.  Please contact Phil Rowe at Hays Energy for more information on phil.rowe@hays.net.nz or call +64 (0) 9 917 8824]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Sat, 02 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob99AA5790B1C379B4482579F50008A03D</referencenumber>
<City><![CDATA[Toronto]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Project-Manager_1666670.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[My client is one of Canadas trusted contractors in construction and Civil engineering.  Presently they are seeking a British or Irish SENIOR PROJECT MANAGER for their offices in Toronto.  The Project Manager is my clients designated representative to the Owner/Client.   The Project Manager, holding experience of projects 20-30 mio,has overall responsibility for the project and the Superintendent.  This position is ultimately responsible for ensuring that a profit is made on the project; that the work is performed as per the contract documents; that the project is completed with outstanding quality; and that the project is a safe workplace.10+ years Project Management experience in the construction industry. University Degree or College Diploma in Civil or Mechanical Engineering/Technology or a combination of education and construction experience. *Computer proficiency - Word, Excel, Outlook, MS Project. Good understanding of quantity surveying. Excellent oral and written communication skills.*Detail oriented. Valid drivers license. Strong code of ethics.*Gold Seal / LEED Certification preferred. This is a permanent position and my client is seeking an individual who is looking to make a life change decision and look to grow within their organisation. The successful candidate will need show a stable work history and will not have moved from job to job on a regular basis]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Senior Scheduler  Oil & Gas]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Sat, 02 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob585B73A4A3F0B247482579F50008A444</referencenumber>
<City><![CDATA[Calgary]]></City>
<Country><![CDATA[CANADA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Scheduler-Oil-and-amp-Gas_1667524.html</url>
<company><![CDATA[TED Recruitment]]></company>
<description><![CDATA[Our client is currently seeks a Senior Project Scheduler to work on a range of large Oil and Gas projects based in Calgary, Canada. Experience of Operations, Turnaround and Shutdowns would be preferred in particular with any experience of oil sands or Shale Gas projects. Responsibilities will including:- coordinate assigned day to day activities and manage scheduling work load with contractors. Build CPM, logically driven construction schedules at various stages of the project life cycle. Specific emphasis is placed on Final Investment Decision (FID) and Issued For Construction (IFC) schedules. Analyze schedule logic, activity durations, constraints, float, resource loading etc. Review critical paths, Level resources as needed to support project constraints. The ability to link detailed engineering and construction schedules with activities to build a complete integrated project schedule. Provide assurance on schedules submitted by contractors according to the project guidelines. The ability to use prior project knowledge to build conceptual schedules is preferred. The ability to develop a schedule risk analysis component of the schedule assurance process. Participate in the interactive planning meetings for projects requesting final investment funding as part of the assurance activity. Understand and use the IPA scheduling metric tool to improve schedule predictability. Incorporate IPA recommendations regarding scheduling into current scheduling process. Help develop, maintain and revise scheduling templates that incorporate all project phases. Help collect and report scheduling information quarterly to support development of the KPI stoplight charts. Perform analysis to track deltas between planned and actual dates and durations. Create a statistical understanding of planned data versus actual outcomes. Assist in progressing construction schedules in accordance with the approved progress measurement strategy. Participate in field walks to validate scope. Help develop and update schedule procedures and work processed as necessary. You will need to have an Engineering Degree or Certification as a Planning / Scheduling Engineer or have equivalent experience. You should be able to demonstrate some industry experience in planning positions. Have good written and oral communication skills. Have good working knowledge of Planning principles and techniques and experience in using Primavera P6. You need to have six to eight years or more experience of working in the Oil and Gas industry. You must be eligible to work in Canada.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Resident Engineer  Romania]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Sat, 02 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob473059194D89A3AB482579F50008A4B1</referencenumber>
<City></City>
<Country><![CDATA[ROMANIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Resident-Engineer-Romania_1667701.html</url>
<company><![CDATA[EWI Recruitment]]></company>
<description><![CDATA[ Resident Engineer is required for Highways Project Romania, working on behalf of European Consulting Firm   The Resident Engineer will have a background in construction supervision of road and bridge construction projects. The client is looking for an RE who has worked on International assignments for consultancies in the past.   Must have good command of the English Language and a BSc in Civil Engineering is essential.This project is for a 24 months and the assignment is to start immediately.   The position will be paying between 3000 - 4000 Euros per month. Unfortunately this is the maximum they can pay and there will be no negotiation form my client.   If you know of any one that may be interested, ewi recruitment do offer a referal bonus. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Senior Advisor Risk Analyst  South Africa]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Sat, 02 Jun 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB926DF4E8F541BD5482579F50008A5A1</referencenumber>
<City><![CDATA[Limpopo]]></City>
<Country><![CDATA[SOUTH AFRICA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Senior-Advisor-Risk-Analyst-South-Africa_1668230.html</url>
<company><![CDATA[Digby Morris]]></company>
<description><![CDATA[Senior Advisor Risk Analyst - Medupi Power Station, Lephalale, Limpopo Province, South Africa Ref: NM/13118  The Project  The Medupi Power Station is a new dry-cooled coal fired power station being built by Eskom near Lephalale in Limpopo province, South Africa. When completed, the power station will have six boilers each powering an 800 MW turbine, producing 4800 MW of power. This will be the largest dry-cooled coal fired power station in the world. At R33.6 Billion, these are the biggest contracts ever placed by Eskom.   Working for the owners engineer, we have an immediate vacancy for a Senior Risk Analyst to be based at the site in the Limpopo Province.        Minimum Requirements  Qualification  *National Diploma in technical environment  Added Advantage:  *Diploma  in Risk Management *Membership of a Professional Risk Institute / Body  Experience:   *7 Years project and Risk Management experience  Added Advantage:  *Demonstrated experience in major construction projects *Power experience  Skills and Competencies Required  *In depth knowledge of Risk Management standards and processes *In depth knowledge of Risk Management systems i.e. CURA, Primavera Risk Analysis) *Skilled facilitator *Attention to detail and ability to accurately capture risk information *Ability to carry out detailed qualitative and quantitative risk analysis *Knowledge or experience of project scheduling *Knowledge or experience of project costing *Strategic thinker with an ability to forecast risk exposure *Ability to clearly communicate and articulate project risk objectives *Negotiation, relationship building and influencing skills *Make sound decisions based on logical and critical examination of given situations  *Attention to detail and a methodical approach to all risk management initiatives  *Excellent conflict handling capabilities *Goal driven with ability to meet monthly reporting deadlines  Key Responsibilities  *Facilitate and ensure Risk Management policies and procedures are understood and implemented *Organise and facilitate project risk workshops *During risk workshops facilitate the process of risk identification, analysis, evaluation and treatment *Prepare and maintain the project risk registers with the output from the risk management workshops *Review and agree the content of each risk register with each risk register owner *Prepare, communicate and report risk information as required / requested *Establish and maintain robust change control over the project risk registers to ensure a clear audit trail *Acts as an advisor to the Project Management team and staff with regards to successful risk management  Benefits  Salary at this stage is highly negotiable, in addition to which the company makes full provision for housing, medical, pension, death in service cover etc.  Please Note  In the first instance preference will be given to applicants already in South Africa or who hold an SA passport, however we welcome applications from all nationalities for the role. ]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience>6 Years And More years</experience>
</job>
<job>
<title><![CDATA[Supply Chain ManagerManufacturingcirca £60,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC4019FDF0DCD5C25482579F5001B72F3</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Midlands West]]></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Manager-Manufacturing-circa-and-amp-SHARP16360000_1639633.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you looking for a challenging new opportunity with a global leader? Do you have a strong background in Supply Chain and Logistics Management? Our clients are looking for the next leader for their site in France due to a change in their business focus. Having previously manufactured the site is now being set up as a hub for distribution in Europe and beyond. The ideal candidate will currently be in a Senior Logistics or Supply Chain role where they are fully involved in change management and continuous improvement. You must be available to travel globally and have worked in a pan-European or global position. To apply you need to speak French to at least business standard but ideally you should be fluent.To apply I will need an updated copy of your CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Planning and Logistics Manager  9 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob48D65CA8699F4288482579F5001B7643</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Planning-and-Logistics-Manager-9-Months_1638486.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Oxford  is currently looking to hire a Planning and Logistics Manager on an Interim basis.You will be responsible for the flow of materials in and out of the business, ensuring that the Master Production Schedule is constantly supported. The successful candidate will have:Significant experience in a similar role in manufacturing or logisticsDetailed MRP experience (MPG pro desirable)Experience with SIOP (Sand#38;OP)Managed 3PLsExperience managing large and diverse teams, and be looking to further your career within this type of environment The successful applicant will:Be responsible for all material movement and stock levelsBe responsible for line management of several team leaders within this functionCreate and control the master schedule for all manufactured productsCoach and support value stream plannersEffectively manage suppliersEffectively manage the dispatch of finished goods to achieve on time delivery and minimise transport costsThe successful candidate will have the chance to join a highly successful and expanding business. If you are interested in applying for this position please send me your up to date CV and if you are sucessful I will call you back to discuss the role further.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT DESIGN ENGINEER REQUIRED]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob541B63EC8CEEEBEE482579F5001B7651</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/URGENT-DESIGN-ENGINEER-REQUIRED_1638500.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Solidworks  Cheltenham]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob75D5260BF8BF1727482579F5001B7660</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Solidworks-Cheltenham_1638513.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Cheltenham  Urgent]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob17074A6ECCDA1C3E482579F5001B766E</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Cheltenham-Urgent_1638518.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent  Cheltenham  Solidworks]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob712F66E89DD641E3482579F5001B7679</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Urgent-Cheltenham-Solidworks_1638521.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Cheltenham  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE68752E68D1817F1482579F5001B7686</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Cheltenham-URGENT_1638524.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Purchasing & Inventory Manager  612 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8908AB6292B5CCE8482579F5001B7693</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Purchasing-and-amp-SHARP38-Inventory-Manager-6-12-Months_1638539.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Apply the purchasing, inventory management and returns process to a pre-defined vendor list ensuring maximum sales throughout, whilst reducing the threat of excess stock.Main repsonsabilities:Achieve targets set by the Senior Procurement and Inventory ExecutiveIn-stock Management - Driving in-stock availability Inventory management - sales and operation planning, capacity planning and inventoryVendor management - Drive vendor compliance, maximise supply chain efficiencies, initiate operational reviewsSupply chain management and#150; workload and capacity planning Liaise and build relationships with key vendor contacts in order to receive timely and accurate information in regards to product availability. Monitor overall stock levels and escalate overstock/under-stock situations.Work with the vendor and sales team to resolve. Maintain the Oracle based system to ensure the most accurate information is always available to the company. The candidate must be:Team player, confident and pro-activeArticulate and focussedEnthusiastic and flexibleMust be able to work on their own initiative and#150; working through set processes as well as using their skills to monitor and review inventory and#150; influencing suppliers to receive stock quickly and in line with customer demands whilst keeping within company guidelines and requirementsExcellent written and oral communication skillsExcellent influencing skillsExperience: At least one year experience in an IT distributor or reseller environment in either product management or purchasing with a proven track history in forecast planningCommercially aware and experienced in influencing decisions that result in priority shipments being receivedMust be both literate and numerate and educated to at least A- Level standardAccurate keyboard skills and#150; must have used MS Excel/Word, bespoke systemsand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Planner]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB74D227B05239BE0482579F5001B76A0</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Planner_1638562.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Luton is currently looking to hire a Supply Chain Leader. This is an excellent opportunity to join a hugely successful, global company with impressive career progression opportunities. You will be responsible for the flow of materials in and out of the business, ensuring that the Master Production Schedule is constantly supported. The successful candidate will have:Significant experience in a similar role in manufacturingExperience working with and developing Kanban and OTDDetailed MRP experience Very strong inventory management experience Experience managing teamsThe successful applicant will:Be responsible for all material movement and stock levelsBe responsible for Inventory ManagementHelp improve OTDBe responsible for line management of several team leaders within this functionCreate and control the master schedule for all manufactured productsCoach and support team The successful candidate will benefit from a salary of up to and#163;50,000 and good package, and the chance to join a highly successful and expanding business. If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAE0F1EDCB7C76CEC482579F5001B76AC</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Manager_1638564.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Luton is currently looking to hire a Supply Chain Leader. This is an excellent opportunity to join a hugely successful, global company with impressive career progression opportunities. You will be responsible for the flow of materials in and out of the business, ensuring that the Master Production Schedule is constantly supported. The successful candidate will have:Significant experience in a similar role in manufacturingExperience working with and developing Kanban and OTDDetailed MRP experience Very strong inventory management experience Experience managing teamsThe successful applicant will:Be responsible for all material movement and stock levelsBe responsible for Inventory ManagementHelp improve OTDBe responsible for line management of several team leaders within this functionCreate and control the master schedule for all manufactured productsCoach and support team The successful candidate will benefit from a salary of up to and#163;50,000 and good package, and the chance to join a highly successful and expanding business. If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Procurement Analyst  Oxford  6  Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFFA3979955635881482579F5001B76B7</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Interim-Procurement-Analyst-and-amp-SHARP150-Oxford-and-amp-SHARP150-6-Months_1638575.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A very exciting opportunity for an Interim Procurement Analyst to join an Oxford based client who are seeking an ambitious and career driven individual.A global organisation based in Oxford are seeking an Interim Procurement Analyst to work as part of an enablement team providing key information to the strategic sourcing function. This is a development role and I am seeking for someone who is very strategic in their way of thinking.  Key accountabilities include: -You will be responsible for analysing the procurement spend across various categories-Advise on improving the analytical tools within the organisation and advise on improving e-sourcing activities-Help train suppliers and manage the on boarding process-Develop collaborative relationships and develop relationships with stakeholders and suppliersMy client is seeking a strategic individual who has worked in a similar role recently and has the passion to make continuous improvements at a fast pace. Please send me your up to date CV and if you are successful I will give you a call back to discuss the role further.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HV Project Planning Role]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF3BCBA72DCD41910482579F5001B76D0</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Midlands East]]></State>
<url>http://www.engineer-job.eu/job/HV-Project-Planning-Role_1638581.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently looking for an experienced hands on Project Planner to work within the power industry.My client has several large on-going projects and is constantly winning new contracts. This enables them to ensure a long secure contract with any Planner they take on.You will be working on substation builds/ refurbishments/ Connections/ Upgrades.You will need to have worked with HV before and have a strong understanding of the industry.Strong P6 experience is essential.The contract is immediate and we are looking to get someone onboard as soon as possible.Rates are negotiable depending on experience.Please send me your updated CV if you are interested and I will contact you. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Supply Chain Director  Thames Valley]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob87D8B74F69414F92482579F5001B76DD</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Interim-Supply-Chain-Director-and-amp-SHARP150-Thames-Valley_1638630.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is currently looking to recruit for an Interim Supply Chain Director to join their highly successful, entrepreneurial business. They are looking for someone to lead the companyand#146;s rapidly growing logistics unit. You will be developing the Supply Chain Infrastructure and will be able to apply their logistics, supply chain, business and management skills.The ideal candidate will have a passion for their work, and enjoy working within a more informal setting. You will also be open to travel, as you may need to travel to secure and develop business opportunities.  The successful candidate will be predominantly responsible for:*Developing and delivering a business plan for the supply chain*Applying their extensive supply chain knowledge to the current business, to redesign and improve systems, processes and procedures*Manage the logistics and warehouses in UK and France*Using their strong business acumen to identify and develop new business opportunitiesThe successful candidate will be able to demonstrate the following attributes:*An extremely strong understanding of supply chain models across industries*Strong communication skills, being able to present confidently. European languages, specifically French, would be an advantage*High levels of knowledge and experience with latest supply chain systems and technologiesPlease send me your up to date CV and if you are sucessful I will call you back to discuss the role in more detail.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Buyer  12 Months  Surrey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1D1E211AAB124713482579F5001B76EC</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Senior-Buyer-12-Months-Surrey_1651560.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is a construction, civil engineering and property services company, with expertise in delivering projects for our clients in affordable housing, commercial property, education, healthcare and transport. They are seeking to recruit a Senior Buyer to join the Group Services Buying Team servicing the Property Services and Rail Maintenance sectors on a meternity cover contract. Key Skills:- Supplier Relationships and#38; Management - External Stakeholder Management - Strong Negotiations- Troubleshooting- Performance Monitoring and#38; Reporting- Comtinuous Improvement- Team Leadership and#38; MotivationYou will support sector teams with efficient purchasing, good product knowledge, aid product evaluation and specification, and be a strong negotiator with good commercial acumen. You will have responsibility and accountability for ensuring agreed processes are followed and our suppliers perform to satisfy the needs of our customers.  As a member of the Reactive Buying team you will contribute to improving purchasing strategies in the reactive maintenance market. You should also be able to demonstrate experience of supervising / supporting Junior members of a team. You will also be able to work under pressure in a fast paced Civil Engineering/Construction environment.The ideal candidate will have extensive experience in a similar role and a good knowledge of the Repairs and Maintenance Market would be essential. Please send me your up to date CV and if you are sucessful I will give you a call back to discuss the role in further detail.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solidworks  Cheltenham 6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob97CF96AC5653BD4F482579F5001B76FA</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/Solidworks-Cheltenham-6-Months_1651575.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT DESIGN ENGINEER REQUIRED  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob94B6D2A3CB2D6945482579F5001B7707</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South West]]></State>
<url>http://www.engineer-job.eu/job/URGENT-DESIGN-ENGINEER-REQUIRED-Contract_1651576.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Cheltenham and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 6 month contract.Due to increased workload and new projects coming to fruition they require additional assistance in the form of two mechanical design engineers to start immediately.The role will revolve around replicating a number of designs already in place and making small amendments and bespoke adjustments.Essential Skills:and#149;Solidworksand#149;AUTOCAD 2DDesirable Skills:and#149;Military experience or Defenceand#149;Interest in the military or defenceRate: MarketLocation: CheltenhamDuration: 6 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager  Modelling & Simulation]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob60AA324DB76BF6CB482579F5001B7AD9</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Midlands East]]></State>
<url>http://www.engineer-job.eu/job/Senior-Manager-Modelling-and-amp-SHARP38-Simulation_1638516.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Position: Senior Manager: Modelling and#38; SimulationLocation: Milton KeynesSalary: Highly Competitive Key Skills: -10 years experience in the application of modelling and simulation technology -Industry experience in aerospace and defence, specialty chemicals, pharmaceuticals, nuclear and fossil power, water, waste water and desalination, food, beverage, personal care, renewable energy or oil and#38; gas-MSC or PHD in engineering or another numerical field with solid knowledge of fluid dynamics-Proven experience in ANSYS fluent, open foam and flowmaster My client are a leading research, product development and design consultancy who specialise in fluid engineering. They work with large international companies in numerous industries including aerospace, energy and manufacturing and are offering a technically engineers the opportunity to join their established team. This is a one off opportunity to work on diverse products and projects in numerous industries and to lead and work with multi-disciplined teams.To apply forthis position please send in your CV to Kirsty McKinnon at Huxley Associatesand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement Manager  Reading  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob427E197F3B8C590F482579F5001B7AE6</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Thames Valley]]></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager-Reading-and-amp-SHARP150-6-Months_1638576.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is looking to take on an Interim Procurement Manager to join their bust and fast paced Purchasing department. The role is an exciting new opportunity to join a large and highly successful business.  The successful candidate will: - Identify material requirements from involvement with projects- Plan purchasing strategy, identify suppliers, engage and implement procurement strategy- Project specific supplier evaluation and selection- Represent supplier agreements in SAP to enable accurate purchasing- Prepare detailed bid documents for supply chain and project purchasing- Manage procurement process on a commission, throughout and to end of project- Use data to report on project procurement cost savings against allowanceThe candidate will be able to: - Procurement: Strong, proven purchasing experience. - Communication: being able to influence suppliers and#38; clients. Understanding business needs and goals to develop strategy and gain buy-in. - Negotiation: Track record in ethical, firm and fair negotiations- Cost Savings- Industry understanding: experience within construction or civil engineeringand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electronic Designer Aberdeen Downhole High Temperature]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE709D7A64E245ABD482579F5001B7BDD</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Electronic-Designer-Aberdeen-Downhole-High-Temperature_1639552.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[OPPORTNITY FOR A SENIOR ELECTRONIC ENGINEER TO PROGRESS AND BUILD UP SALLARY- FUTURE MANAGEMENT OPPORTUNITYAre you looking for a new position with a large Oil and Gas Company in Aberdeen who are known internationally? I am currently looking for a Senior Electronics Engineer/ Designer to join an established and growing company in Aberdeen. They are looking for someone to come on board and grow within the company. This is an urgent requirement. On top of the progression available, this company pay one of the highest salaries in Aberdeen for people with this background. This is a fantastic opportunity. PLEASE APPLY NOW!.  The Roleand#149;The right candidate will play a key role in the design, development and testing of new data acquisition products as well as working on existing productsand#149;You will play a key role in the department and#149;Coaching/ ManagementThe PersonEssential:and#149;Design experienceand#149;Strong Electronic backgroundand#149;Microcontroller software development experienceand#149;PCB Design experienceDesirable:and#149;Electronics degree or similar disciplineand#149;High Temperature electronic design experience Unfortunately there is no funding available for sponsorship. If you are interested please send me your CV ASAP. Interviews will be taking place Friday this week and Monday next week. They are looking to get the right person on board as soon as possible.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Management, Manuf, NW, into Oil & Gas]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5CA3BD499B307063482579F5001BA2ED</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Management-Manuf-NW-into-Oil-and-amp-SHARP38-Gas_1651549.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently looking to recruit for two Senior Management roles in the North East and I need Candidates that have worked in the high end of Management and worked for companies that supply into the oil and#38; Gas Sector.This is a little vague at present as I need to get some bench mark candidates over but also because I am trying to get together some brilliant candidates to sell to key clients in that areaand#133;..so please apply and I will give you a call and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Executive NHS & Local Government 90k 0TE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob60CD58DBC45FB845482579F5001BA2FB</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Executive-NHS-and-amp-SHARP38-Local-Government-90k-0TE_1651550.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to be part of an ambitious and entrepreneurial company who are looking to aggressively grow in size. They now have a requirement for a Sales Execs to join the company. The focus would either be on the NHS or Local Government Ideally you will have experience selling IT Software solutions and have worked in all parts of the sales process including Account Management and Business Development. Experience with selling CRM systems would also be beneficialThe company are looking to make an Initial Public Offering within the next 5 years and this role offers the candidate the opportunity to get involved with equity participation and eventual company directorship. The role would require the candidate to be based from Woking and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Engineer ~ Labview ~ Urgent]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEA6137DEEF239A6C482579F5001BA30F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Engineer-~-Labview-~-Urgent_1651551.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently recruiting for a Labview Software Engineer to begin a 6 month contract in the Milton Keynes area. The company Huxley Associates are working with have a significant amount of work over the next couple of years and need high quality Software Engineers to propel them forward. The contract is initially 6 months but has a strong chance of continuing.Please find the brief outline of the vacancy below: Lab View Software engineer. Tasks: Using a documented Software Map and working with an existing software engineer write Labview code for an HMI controlled Class IIb medical device conforming to appropriate Global Standards. Document the process and code to the necessary Global Standards. Applicant will need to work to a deadline both independently and in close coordination with the existing project software and hardware engineers.  Experience: Preferably Labview certified. Preferable previous medical experience in class IIb or above. Examples of previous software using touch screen user interface (HMI) would be an advantage. Use of Solidworks would be an advantage but not essential. Should you wish to hear more or apply for the position, please get in contact on the details below. Please also ensure I have a up to date CV. The company are looking to telephone interview this week and hope to start the right person as soon as possible. Please also indicate when you can telephone interview this week.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[General Manager Ops: Nuclear]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEDE14FB061B99ED3482579F5001BA31C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/General-Manager-Ops:-Nuclear_1651552.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am looking to recruit Senior Management who has experience of running a fabrication and/ or engineering company supplying into the Nuclear Sector. I have roles coming up in both the North West and Yorkshire and the salaries are very very broad. Please note this is a real area of growth, so if you have exposure to this sector or if you looking to move into this sector, please apply I am ideally looking to work with candidates in the 60k + bracket, although I will consider candidates outside of this bracket. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regional Sales Manager Germany up to 75000 Euros]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB1A92C575BE5706482579F5001BA32A</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regional-Sales-Manager-Germany-up-to-75000-Euros_1651553.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you currently based in Germany or willing to relocate?If so to both questions then I have an excellent opportunity for you as a Sales Manager for Germany.The role is working for a subsidary for one of Americas largest organisations. The company are involved within the machinery industry and have experienced significant growth over the last couple of years. More growth is expected in 2012. Role:Manage Key Accounts and#38; OEMs with a specific focus on wide web OEMsIdentify and establish new OEM and key account businessIdentify and develop 3rd party distributors Support End users in specific marketsExperience:Fluent German and#38; English Based in GermanyExperience of machinery industryKey Account Management experienceTechnical BackgroundThe package on offer is up to 75k + 30k Bonus + Car etcand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PLC Controls Engineer Yorkshire 6 Month Rolling Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob03EAF23EA2ACE8FD482579F5001BA336</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PLC-Controls-Engineer-Yorkshire-6-Month-Rolling-Contract_1651554.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client based in the North East has immediate requirements for 2 Control Engineers on a contract basis for their offshore projects, although you may not be required to go offshore. Must has experience in developing PLC software for major manufacturers such as Rockwell, GE and Siemens. Experience in developing SCADA software for major manufacturers including Wonderware, Rockwell and GE . Ideally have proven experience of working in the Oil and Gas industry on offshore projects and be familiar with Functional Safety and developing systems in accordance with IEC 61508 / 61511. Ability to analyse user requirements and formulate a solution. Ability to create technical specifications and test plans. Possess the aptitude for future professional development with a view of taking on Senior project engineer responsibilities. Have the ability to manage time and organise workload to meet deadlines. Interviewing Now!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Site Supervisor Grangemouth 12 Month Rolling Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF58FF12BDCB632F6482579F5001BA343</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Site-Supervisor-Grangemouth-12-Month-Rolling-Contract_1651555.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client specialising in the construction and refurbishment of tank systems to the Oil and Gas industry have an immediate requirement for Site Supervisor on an ongoing contract basis. You will be experienced with projects involving fabrication, piping, mechanical installation and steelworks supervising teams up to 20+.  You will ideally be educated within a mechanical discipline or have the relevant experience in supervising similar projects on time, within cost and safely. Candidates with a CCNSG 2 day site passport would be preferable although not essential.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QS  Pembroke  12 month Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA750867BA8D908A2482579F5001BA378</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QS-Pembroke-12-month-Contract_1651558.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quantity Surveyor/Estimator We seek to recruit an experienced individual familiar with a range of Mechanical Services estimating, experience in the field of pipe work, structural steel and bulk tank storage would be beneficial, Communication, numeracy and computer skills are all paramount to this role. Duties will include initial estimation and tender preparation of multiple projects, continuing through to measurement and valuation of works in progress and participation in the management of the supply chain to ensure the overall financial success of a project.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Microstation CAD Technician, Warwickshire, 6 Months, Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAF7450AB2E11D164482579F5001BA387</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Microstation-CAD-Technician-Warwickshire-6-Months-Negotiable_1651559.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Microstation CAD Technician, Warwickshire, 6 Months, NegotiableWorcestershire based client is currently recruiting for a Microstation CAD Technician for a 6 month project. Candidates will be proficient in the use of Microstation and have experience of plant layout. Candiates will be involved in the design of spray booths and plant layout.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Catia V5 Design Engineer, Worcestershire, 3 Months, Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob00357236A86D28E8482579F5001BA395</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Catia-V5-Design-Engineer-Worcestershire-3-Months-Negotiable_1651561.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Catia V5 Design Engineer, Worcestershire, 3 Months, NegotiableMy Worcestershire based client is currently recruiting for a Catia V5 Design Engineer. They are looking for candidates who are proficient in the use of Catia V5 and ideally have an understanding of Unigraphics NX. Ideal candidates will have automotive and preferably Off-Highway vehicle exposure. They will be involved in the design of latches, hinges, and door locks for the automotive industry. Candidates will have a knowledge of small mechanisms, injection moulding, pressings, stampings etc.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Planner  South Wales  Oil and Gas]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3607402431EF1E02482579F5001BA3A3</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Planner-South-Wales-Oil-and-Gas_1651562.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[We seek to recruit an experienced planner to work within the mechanical engineering industry.  Knowledge of Microsoft Project is also important.  You will have an active role within the preconstruction phase of projects and have an input in the construction phase.  You will provide a planning and programming service for primarily pre-contract and some post contract works.  You will be responsible for production of competitive and realistic tender plans, programmes and contract programmes.  You will have a thorough understanding of projects, scope of works and restrictions imposed by contractual requirements, and site conditions.  Knowledge of Microsoft Project and Primavera is important.   and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Planner  Mining  London]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0380B5862BE55011482579F5001BA3AE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Planner-Mining-London_1651563.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am looking for Project Planning Engineer to work on a 12 month Project in London. Candidates must have Planning experience using P6 and must have mining experience.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE3FE670871C5675482579F5001BA3BD</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-Manager_1651564.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Senior Regulatory Affairs ManagerBranche: Chemie Locatie: regio GeleenSalaris: 80-120kFulltime (geen ZZP-ers!)Voor een internationaal chemisch bedrijf in de region Geleen is Huxley Associates urgent op zoek naar een Senior Regulatory Affairs Manager.Taken en verantwoordelijkheden:- Je geeft leiding aan een team circa 10 specialisten - Je bent verantwoordelijk voor de registratie, classificatie, labeling en safety data sheet voor de producten in het EMEA gebied- Je beheert de budgetten en zorgt ervoor dat de producten gereed zijn voor de komende wetgeving (REACh)- Je assisteert de Global Rand#38;D DirectorProfiel:- MSc/ PhD in Agronomie- Minimaal 8 jaar relevante werkervaring- Leidinggevende ervaring- Uitstekende beheersing van de Nederlandse en Engelse taal in woord en geschrift. Beheersing van een derde Europese taal in een enorme preInteresse? Reageer dan nu ter attentie van Daniel de Keyzer van Huxley Associates via dde onderstaande link. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Pro E  Plymouth]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2D4F53C55E9C8237482579F5001BA3C9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Pro-E-Plymouth_1651565.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Plymouth and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range.Essentials:and#149;Pro Engineer as main CAD Package (Wildfire 4 Desirable)and#149;Injection Moulding experienceand#149;Plastics Experienceand#149;FMEA Experienceand#149;Experience of Design Reviewand#149;Excellent communication skills with the ability to interact at all levels and is a pro-active team member. and#149;Communication skills include written reports, presentations and cross-functional team activity. Responsibilities:and#149;Finishing off the 3D Designsand#149;Providing the Mechanical Analysisand#149;Providing the Design ReviewThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Rate: MarketLocation: PlymouthDuration: 3 Monthsand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob270313CDD8FBDD48482579F5001BA3D8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer_1651566.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design Engineer - East Sussex - 3 month Contract Responsible for Design work at conceptual phase: -AutoCAD LT/Autocad Electrical experience required. -Specifying components. -Cable calculations. -Design documentation/design verification. -Pand#38;IDs. -Schematic Capture, instrumentation. If you are interested in a new contract opportunity then please apply.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Plymouth]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob288CE783DAC7F57A482579F5001BA3E8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Plymouth_1651567.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is looking for a Mechanical and Electrical Engineer to meet the expanding workload in our Plymouth Office. The successful candidate will:and#149;Have experience of seeing conceptual designs through to completion and#149;AutoCAD; Hevacomp, Relux Pro and NES and have a working knowledge of IEE regulations 2011 edition and CIBSE Guidesand#149;Be MCIBSE or MIET qualified and#149;Have a strong ethical approach to safety, quality and environmental protection. Salary is on offer up to and#163;40,000 + benefits. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Building Services Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA3B23EE484BEC8A0482579F5001BA3F8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Building-Services-Engineer_1651568.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is looking for a Mechanical and Electrical Engineer to meet the expanding workload in our Plymouth Office. The successful candidate will:and#149;Have experience of seeing conceptual designs through to completion and#149;AutoCAD; Hevacomp, Relux Pro and NES and have a working knowledge of IEE regulations 2011 edition and CIBSE Guidesand#149;Be MCIBSE or MIET qualified and#149;Have a strong ethical approach to safety, quality and environmental protection. Salary is on offer up to and#163;40,000 + benefits. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Building Services Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA86046E6F2A3BEBD482579F5001BA404</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Building-Services-Engineer_1651569.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is looking for a Mechanical and Electrical Engineer to meet the expanding workload in our Plymouth Office. The successful candidate will:and#149;Have experience of seeing conceptual designs through to completion and#149;AutoCAD; Hevacomp, Relux Pro and NES and have a working knowledge of IEE regulations 2011 edition and CIBSE Guidesand#149;Be MCIBSE or MIET qualified and#149;Have a strong ethical approach to safety, quality and environmental protection. Salary is on offer up to and#163;40,000 + benefits. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Pro E  Plymouth]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF05E9BD5B5837D9E482579F5001BA413</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Pro-E-Plymouth_1651570.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Plymouth and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range.Essentials:and#149;Pro Engineer as main CAD Package (Wildfire 4 Desirable)and#149;Injection Moulding experienceand#149;Plastics Experienceand#149;FMEA Experienceand#149;Experience of Design Reviewand#149;Excellent communication skills with the ability to interact at all levels and is a pro-active team member. and#149;Communication skills include written reports, presentations and cross-functional team activity. Responsibilities:and#149;Finishing off the 3D Designsand#149;Providing the Mechanical Analysisand#149;Providing the Design ReviewThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Rate: MarketLocation: PlymouthDuration: 3 Monthsand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Product Design Role Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob485B51BB78DACF41482579F5001BA422</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Product-Design-Role-Bath-and-amp-SHARP16340000_1651571.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a senior product design engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project planner  East Midlands  Power 6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCEC47298DFFFD02C482579F5001BA42D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-planner-East-Midlands-Power-6-Months_1658582.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently looking for three project planners to work on Coal Fired power station Shutdown projects for one of the largest energy companies in the UK.There a several large projects coming up which will allow the successful candidate to have a long lucrative contract.I am looking for three hands on planners that have strong site experience and a solid understanding of P6.Coal fired power station experience will be very useful as the projects are coal fired, similar experience on power stations will be useful.Working in a fast paced environment so you will need to be in good healthYou will need to have an engineering background and have the ability to commute to and from site.The contract will be for an initial 6 months with the option to renew.Contact me immediately so you do not miss out on this position. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Bristol  Contract  SUBSEA  Engineering]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1B2342338D6A0603482579F5001BA43C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Bristol-Contract-SUBSEA-Engineering_1658583.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerDesirable:and#149;Subsea experienceand#149;Subsea sensing equipmentRate: MarketLocation: Bristol and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Bristol  3 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4061BB85267721E5482579F5001BA449</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bristol-3-Months_1658584.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerDesirable:and#149;Subsea experienceand#149;Subsea sensing equipment This is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Please send your CV in for immediate consideration.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pro E  Gloucester  6 Month Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB8D68D3717C3FF8482579F5001BA45E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pro-E-Gloucester-6-Month-Contract_1658585.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Gloucester and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new projects regarding a new  product range as well as bespoke changes to existing products.Essential Skills:and#149;Experience with Pro Engineerand#149;Experience with Solidworksand#149;Work to British / Pan American Standardsand#149;5 Years experience within Mechanical Design Desirable Skills:and#149;Experience with Valve Systemsand#149;Experience with ActuatorsRole:and#149;Developing 3D Models of Valve componentsand#149;Produce Documentation ( BOM and Engineering Change Orders)and#149;Produce calculations in support of designs and#149;Liaise with ManufacturingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role.Rate: MarketLocation: GloucesterDuration: 6 Months with possible extension.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Design Engineer  Mechanical]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCD5A07DA32988953482579F5001BA46B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Principal-Design-Engineer-Mechanical_1658586.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Principal Mechanical Design EngineerLeicesterCirca and#163;40-45,000 and BenefitsInternational travel included. This growing business seeks a principal engineer to support the technical manager with existing workloads. You will be a senior member of the design team taking responsibility for existing and upcoming projects and working closely with key clients. You will work across a number of projects at any one time from existing product improvements to new product developments.   This will be a handand#146;s on role for an innovative engineer; with responsible for generation and delivery of concept and manufacturing designs. Responsibility will also be held for planning, controlling and delivering assignments to plan and within budget. You will need to work closely with customers and suppliers.  Skills Needed: FEA AnalysisMS Office and#38; MS Project 3D CAD experience: Pro-E/ Solid Works Experience in a fast moving industry: i.e. consumer electronics, food, packaging, dispensing equipment etc beneficial To apply for this vacancy please send in your CV ASAP to avoid disappointment.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Gloucester  Valves]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6DB76349968EC3E0482579F5001BA47A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Gloucester-Valves_1658587.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Gloucester and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new projects regarding a new  product range as well as bespoke changes to existing products.Essential Skills:and#149;Experience with Pro Engineerand#149;Experience with Solidworksand#149;Work to British / Pan American Standardsand#149;5 Years experience within Mechanical Design Desirable Skills:and#149;Experience with Valve Systemsand#149;Experience with ActuatorsRole:and#149;Developing 3D Models of Valve componentsand#149;Produce Documentation ( BOM and Engineering Change Orders)and#149;Produce calculations in support of designs and#149;Liaise with ManufacturingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role.Rate: MarketLocation: GloucesterDuration: 6 Months with possible extension.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Operations Manager  World Leading OEM  £60,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEE8C1BC61622B77D482579F5001BA485</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Operations-Manager-and-amp-SHARP150-World-Leading-OEM-and-amp-SHARP16360000_1658588.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you an experienced Operations Manager?Would you like the opportunity to work for a World Leading OEM?One of the top manufacturing and engineering companies in the UK are offering a select candidate the chance to be part of this technically intense and strategically focused firm. The company, who design, develop and manufacture on site, require a new Operations Manager to join the team. Interested in this opportunity? You will need to be a proven Operations Manager with experience within Welding, Fabrication or Machining environment. You will have 5 direct reports (Group Leaders) and a total of 284 indirect reports. You will report directly to the General Manager and be responsible for OEE, Capacity planning, efficiencies, TPM, labour cost and production improvements.With sites throughout the UK and the World, there is a huge amount of opportunity to develop your career. You will also be working at their state of the art site with onsite gym and over 2000 employees.  Despite that this is a company in which every employee has an overwhelming sense of identity, they are proud to work for our client and stop at nothing to deliver to the customer. With no exceptions you must bring the same ethos to the role.In return for you knowledge and expertise, you can expect the opportunity to develop a long term and challenging career within a secure and ever growing organisation. This position is offering a salary of circa and#163;60,000 plus benefits.So if you fit all of the above stated requirements and more, please get in touch ASAP. This is an urgent vacancy and you must hurry if you wish to join a company that is going from strength to strength.NB:May suit individuals with a background as (but not limited to): Operations Manager, Operations Director, Manufacturing Manager, Manufacturing Director, Production Manager, Production Director.This position is commutable from:Uttoxeter, Stoke on Trent, Birmingham, Burton on Trent, Derby, Nottingham, Loughborough, Leicester, Telford and Wolverhampton.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PRO E Design Engineer  East Midlands  £2530hr]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE29B9B7ACD9AC23A482579F5001BA491</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PRO-E-Design-Engineer-and-amp-SHARP150-East-Midlands-and-amp-SHARP16325-30-hr_1658589.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client based in the Midlands has an immediate requirement for a Design Engineer.Ideally the candidate will have previous experience of transmission, gears and engine design.The contract is initially for 6 months with a further 6 months thereafter and is paying an hourly rate of and#163;25-30/hour depending on experience.An Automotive or yellow goods (ie. JCB or Caterpillar) background would be a distinct advantage.My client is looking for a candidate who has a sound knowledge of Pro Engineer but would consider candidates who have good experience of Catia V5 along with an Automotive background.You will also have the option of completing your hours over 4 days and getting every Friday off.Must have good communication and presentation skills as the position will be required to liaise with the client and suppliers. Ideally educated to a degree level or the equivalent in experience. Interviewing NOW! and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Contract  SW]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3CC2043B0D8FECF8482579F5001BA49E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Contract-SW_1658590.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Gloucester and#150; 6 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new projects regarding a new  product range as well as bespoke changes to existing products.Essential Skills:and#149;Experience with Pro Engineerand#149;Experience with Solidworksand#149;Work to British / Pan American Standardsand#149;5 Years experience within Mechanical Design Desirable Skills:and#149;Experience with Valve Systemsand#149;Experience with ActuatorsRole:and#149;Developing 3D Models of Valve componentsand#149;Produce Documentation ( BOM and Engineering Change Orders)and#149;Produce calculations in support of designs and#149;Liaise with ManufacturingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role.Rate: MarketLocation: GloucesterDuration: 6 Months with possible extension.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lean Manager  Leading global company]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB5CDE7D9C989BD68482579F5001BA4AA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lean-Manager-and-amp-SHARP150-Leading-global-company_1658591.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is pleased to be working a an absolute market leader within Engineering who are looking for a new Lean Manager to join the site. This is an outstanding opportunity as it is a brand new role for the business so a real chance to make the role your own. Being part of a large group the opportunities are endless for the right person.This is a company with over 200 people on the site in Derbyshire where the role is based. Lean has always been a focus within the company but within other peoples roles. As a business they are now keen to take this to the next level and have a permanent person with a full focus in the role and this is backed fully by senior management.Interested? We are looking for some of the best Lean Managers within the industry. You must have proven experience in a similar role ideally implementing lean principles from scratch. Industry experience is flexible but any automotive, fmcg or manufacturing experience would be very desirable. On offer for the role is a starting salary of circa and#163;50,000 plus a generous benefits package which is flexible dependant on the successful candidates skills and experience. This is an urgent role with shortlisting occurring now so if you would like to be considered please apply online to Brooke Whitehead at Huxley Associates asap in order to avoid disappointment.NB This role may be suitable for, but is not limited to, the following job titles: Lean Manager, Continuous Improvement Manager, Six Sigma Black belt, Lean Practitioner or Business Improvement Manager.This role is commutable from: Derby, Sheffield, Chesterfield, Alfreton, Mansfield, Matlock, Nottingham, Derbyshire, Nottinghamshire, East Midlands. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Client Director  Central Government 100k OTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDCE00BF339390642482579F5001BA4B7</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Client-Director-Central-Government-100k-OTE_1658592.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to work for a Not for Profit organisation who have grown by 20% year on year since they were established. Providing Cloud and IT Services to the Public Sector my client has ambitious plans for future growth. Due to this growth they now have an excellent opportunity for a Client Director to look after one of there largest Government Accounts Reporting to the Business Development Director the role will be to further grow the Provision of Web services and hosting in addition to Cloud based services. You will be maintaining C Level,Director Level and Operational Level relationships within this Account. Looking for ways of growing the business/income opportunities within this key account is vital. You will also be responsible for developing the Account Strategy for this client. You will ideally have a proven track record in Consultative selling of IT Services/Application Development or Business Consultancy., with a proven track record in managing large Central Government Accounts A technical or Pre Sales background would also be desirable. Experience of the Education sector would also be desirable. Degree Educated would also be desirable This is an excellent opportunity to join a rapidly growing organisation who also offer a Final Salary Pension scheme. The ideally candidate will either be based in the South East or South West. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Business Manager  Central Gov Sales 100k OTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA1174855350C97D2482579F5001BA4C4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Business-Manager-Central-Gov-Sales-100k-OTE_1658593.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to work for a Not for Profit organisation who have grown by 20% year on year since they were established. Providing Cloud and IT Services to the Public Sector my client has ambitious plans for future growth. Due to this growth they now have an excellent opportunity for a New Business Manager to source new opportunities within Central and Local Government.  Reporting to the Business Development Director the role will be to further grow the Provision of Web services and hosting in addition to Cloud based services. Responsibilities: Leading the company sales strategy for Central and#38; Local Government Leading the identification of new sales opportunities in Government Owning the relationship with existing and new Government clients Your Experience: Experience of securing new business with Government or Public Sector clients Ability maintain strong relationships with clients Successful track record in Consultative selling of IT Services and Solutions Proven track record of exceeding Sales Targets This really is an excellent opportunity to grow a rapidly expanding company who also offer a Final Salary Pension scheme. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Design Engineer (Machinery) Hull  York]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob973F8A3D0537F1D6482579F5001BA4D1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Design-Engineer-Machinery-Hull-York_1658594.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Senior Mechanical Design Engineer: East Yorkshire (Hull / York / Scarborough)One of the UKand#146;s leading Special Purpose Machinery Houses are looking to recruit a Senior Mechanical Design Engineer on a permanent basis for their site based in East Yorkshire. An out and out Senior Design Engineer, the Senior Design Engineer should have experience / understanding of the full design lifecycle (concept and#62; modelling and#62; detail and#62; assembly) and from working in fast paced, dynamic environment. Ideally coming from an apprentice background, the Senior  Mechanical Design Engineer will have prior experience of fabrication and designing product / machines with and#147;moving partsand#148; (drives, motors, gears, switches etc), not just static products. In addition, the Mechanical Design Engineer should have experience of 3D Design and#38; Modelling (ideally in SolidEdge, through SolidWorks, AutoCAD, Inventor etc will also be required).  Prior experience of machine design / special purpose machinery / automated equipment is required for this Senior Mechanical Design Engineer role and the Senior Mechanical Design Engineer must have previous experience of taking ideas, researching them and bringing / developing new design / machines. In addition, Rand#38;D experience would be of benefit for this role. An articulate and effective communicator, the Senior Mechanical Design Engineer should be a confident, proactive individual who can work in a customer facing and demanding environment and be a driven individual, who wants to work at the cutting edge of machinery design . For the successful Senior Mechanical Design Engineer, a salary reflective of experience is on offer. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Group Quality Manager  Birmingham]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob47F48526352AFC17482579F5001BA4E1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Group-Quality-Manager-Birmingham_1658595.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is proud to be working with a leading global Automotive manufacturer based in Birmingham. As a business they are truly global with sites throughout the Americas, Europe and Asia. As a tier 1 Automotive company they supply to a large number of OEMs.Due to a promotion they are looking for a new Quality Manager to join their Senior Management team. The role will report directly to the Plant Director and be responsible for all aspects of Quality on site.We are looking for some of the best Quality Managers within the Automotive industry. Ideally you will have an Automotive background and a lead auditor to TS16949. Most importantly though you will need a and#147;can- doand#148; spirit and strong communication skills. This is a company which can not only offer security but also long term career progression to the right candidate.On offer for the role is a starting salary of circa and#163;55,000 plus a generous benefits package which is negotiable dependant on the successful candidate.Interested? This is an urgent role with interviews being lined up now so if you would like to be considered please apply online to Brooke Whitehead at Huxley Associates ASAP in order to avoid disappointment.NB This role may be suitable for, but is not limited to, the following job titles: Quality Manager, Quality Director, Senior Quality Engineer, QHSE Manager, SHEQ Manager.This role is commutable from: Birmingham, West Midlands, Worcestershire, Warwickshire, Coventry, Staffordshire, Telford, Leicestershire, Derbyshireand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ProjectSenior Design Engineer Opportunity]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAD7437D6D205CC50482579F5001BA4EF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Senior-Design-Engineer-Opportunity_1658596.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Role: Project/Senior Design Engineer Industry: 1st tier automotive Location: DudleyMy client an international manufacturer supplying to leading OEMand#146;s in the automotive industry seek a hands on design engineer for a project engineer vacancy. This will include cradle to grave project management and#150; working with the customer taking the design requirement, 3D CAD design and overseeing the New Product development through to delivery. A small amount of travel may be included. To be successful in this role you will be an experienced mechanical design engineer who has worked within the automotive industry, a strong understanding of mechanism design would be highly beneficial as would any experience of Catia V5. In return they are offering a competitive salary, pension contribution and private healthcare. To apply for this role please send in your CV ASAP.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0C9CB25C8912A16D482579F5001BA4FE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager_1658597.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Managerand#150; Berkshire - circa and#163;35,000 -and#163;45,000Huxley Associates are working with a large multinational organisation in Berkshire to recruit for Project Manager position. Our client operates within the food and beverage industry providing to a global region. They understand that employees are vital to the progression of the company and as such are seen as key assets.Job Details:The key responsibilities are manager engineer lifecycles from initial concept across supporting manufacture to commissioning.ExperienceThe main attributes to be seen on a CV are the following:-Background within the food industry-Experience in a project engineering or project management role and#150; at least 3 years-Degree qualified or equivalent within mechanical or chemicalYou may have experience in the following roles: Project Management, Project Leader, Delivery Project Manager, Project Engineer Salary: circa and#163;35,000 -and#163;45,000 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Siemens WinCCRockwell Engineer Bristol £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCCA5A5830F86177D482579F5001BA51B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Siemens-WinCC-Rockwell-Engineer-Bristol-and-amp-SHARP16340000_1658599.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a PLC/SKADA software engineers to be a permanent addition to their team. This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;40,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PLCSKADA Engineer Bristol £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9D5FD44565CCE9A482579F5001BA529</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PLC-SKADA-Engineer-Bristol-and-amp-SHARP16335000_1658600.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a PLC/SKADA software engineers to be a permanent addition to their team. This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;35,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Siemens WinCCRockwell Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1E1A94B63625F04D482579F5001BA53F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Siemens-WinCC-Rockwell-Engineer-Bristol_1658601.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a PLC/SKADA software engineers to be a permanent addition to their team. This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;35,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PLCSKADA Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3E355A749A95A229482579F5001BA554</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PLC-SKADA-Engineer-Bristol_1658602.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a PLC/SKADA software engineers to be a permanent addition to their team. This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;35,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CMM Engineer, Worcestershire, 6 Months, Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob47417D6079799AF0482579F5001BA563</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CMM-Engineer-Worcestershire-6-Months-Negotiable_1658603.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[CMM Engineer, Worcestershire, 6 Months, NegotiableMy Worcestershire based Aerospace client is currently recruiting for a highly skilled CMM Engineer for an initial 6 month contract. They are looking for candidates who are proficient in the use of Mitutoyo Cosmos. The role:Programming and running CMM MachinesComplete capability studies and Gauge Rand#38;R studies when requiredCompleting inspection reports using CMM machineThis is an immediate requirement. Interviews will be taking place next week with a view to an immediate start.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Applications Engineer (Mechanica) Huddersfield]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7F714D9B04BB79FE482579F5001BA576</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Applications-Engineer-Mechanica-Huddersfield_1658604.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Applications Engineer (Mechanical Engineering Design / Project) Wakefield / Huddersfield / HalifaxOne of the UKand#146;s leading suppliers to the Oil and#38; Gas Industry, providing engineering solutions for rotating equipment are looking to recruit an Applications Engineer (Mechanical Engineering) to join the Engineering Applications Team on a permanent basis at their West Yorkshire site. With the Applications Engineer (Mechanical Engineering) role being split 50/50 between Design and#38; Sales, the Applications Engineer (Mechanical Engineering) should have a strong client facing ability, possessing experience of the full design / project lifecycle, from initial client contact / specification through to delivery of product. A strong knowledge of 3D Design in AutoCAD and#38; SolidEdge is required for this role, as is prior experience of Calculations / FEA Data Analysis and#150; However, detailed design will be undertaken by design draughtsman.  Working on projects ranging from and#163;10k-100k, the Applications Engineer (Mechanical Engineering) will be working on multiple projects at any one time and must have a prior experience of working in a client facing environment and be an articulate, effective and confident communicator. A strong knowledge of Mechanical Engineering (ideally experience of coupling, rotating equipment, pumps, gears etc) is also required for this Applications Engineer role. For the successful Applications Engineer (Mechanical Engineering), a salary reflective of experience is on offer. To be considered for this Applications Engineer role, please apply via the link below. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Merchandiser, Fashion, regio Haarlem]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC2F6FB0DD0890C1D482579F5001BA587</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Merchandiser-Fashion-regio-Haarlem_1658605.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Onze opdrachtgeverVoor een van onze opdrachtgevers, een gerenommeerde kledingfabrikant, zijn we op zoek naar een nieuwe Merchandiser.De functieAls Merchandiser ben je verantwoordelijk voor een merkenpakket binnen het bedrijf. Je bent verantwoordelijk voor de gehele productiebegeleiding. Je bespreekt bestaande en nieuwe modellen met onze klant, verwerkt hetgeen besproken is and#38; communiceert deze terug naar de kantoren en fabrieken in de verschillende productielanden. Het is dus essentieel dat je modebewust bent en over technische kennis beschikt.  De functie-eisenVoor deze functie is ruime ervaring op het gebied van productie, productontwikkeling and#38; het opstellen van maatschemaand#146;s vereist. Je bent sterk in het onderhouden van contacten and#38; het onderhandelen met de fabrikanten. Je bent nauwkeurig en hands-on, bovendien ben je altijd op zoek naar verbeteringen. Je beschikt over een HBO werk-en denkniveau en je beheerst de Engelse taal uitstekend. Ben je enthousiast geworden na het lezen van deze vacature, en sluit jouw profiel aan op bovenstaande eisen? Reageer dan direct met een up-to-date cv via onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Productiemanager, Fashion, regio Haarlem]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB922B204716F6E10482579F5001BA597</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Productiemanager-Fashion-regio-Haarlem_1658606.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Onze opdrachtgeverVoor een van onze opdrachtgevers, een gerenommeerde kledingfabrikant, zijn we op zoek naar een nieuwe productiemanager.De functieAls productiemanager ben je verantwoordelijk voor een merkenpakket binnen het bedrijf. Je bent verantwoordelijk voor de gehele productiebegeleiding. Je bespreekt bestaande en nieuwe modellen met onze klant, verwerkt hetgeen besproken is and#38; communiceert deze terug naar de kantoren en fabrieken in de verschillende productielanden. Het is dus essentieel dat je modebewust bent en over technische kennis beschikt.  De functie-eisenVoor deze functie is ruime ervaring op het gebied van productie, productontwikkeling and#38; het opstellen van maatschemaand#146;s vereist. Je bent sterk in het onderhouden van contacten and#38; het onderhandelen met de fabrikanten. Je bent nauwkeurig en hands-on, bovendien ben je altijd op zoek naar verbeteringen. Je beschikt over een HBO werk-en denkniveau en je beheerst de Engelse taal uitstekend. Ben je enthousiast geworden na het lezen van deze vacature, en sluit jouw profiel aan op bovenstaande eisen? Reageer dan direct met een up-to-date cv via onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Production Engineer (Bournemouth) £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC026B2C36AB48A6A482579F5001BA5A5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Production-Engineer-Bournemouth-and-amp-SHARP16335000_1658607.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is a leading company in the Oil and#38; Gas.The JobMy client is looking for a Production Engineer to ensure that all production drawings and associated documents are accurate, complete and available for efficient and timely manufacture of products.Person Specification:Experience within a manufacturing company; background of work with manufacture and/or assembly of PCBs preferred.Comprehensive understanding of electro-mechanical manufacturing processes. Experience of using MRP/ERP business systems (SAP preferred) for production engineering.Qualified to at least HNC in engineering; degree qualification preferred.Strong analytical and problem solving skilGood inter-personnel skills including active listening but decisive and able to influence and convince others to adopt a specific course of action.Adaptable and flexible approach Salary: to and#163;35,000 Plus BenefitsTo apply, please attach your CV and/or call Akeela Tuffail on 0118 956 5545 for an immediate response.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Embedded Engineer  Oxfordshire  Circa £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9EB6FE5637821636482579F5001BA5BA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Embedded-Engineer-Oxfordshire-Circa-and-amp-SHARP16340000_1658608.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for a number of Embedded Engineerand#146;s to join my client based in Oxfordshire. Salary circa and#163;40,000.My client has built on its expertise in high speed memory to become a dominant player in the manufacturing and distribution of solid state drives (SSDs).My client also offers high performance components for computing devices and systems,including enterprise class power management products and industrial power accessories.The key to being a successful candidate for this role is to be a good problem solver. Without this you will not be considered.You will have experience in a demanding, resultsand#150;oriented environment closely related to that of the technology used by my client. You would have also been in positions which involve you talking down to the registers. You must have extensive experience in the following:- Extensive experience in C and/or Assembler - Experience in Embedded environments- Experience with ARM OR Cortex]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electronics Design Engineer  Surrey  Circa £50,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob77FEAB9F0C533A77482579F5001BA5C7</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electronics-Design-Engineer-Surrey-Circa-and-amp-SHARP16350000_1658609.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for an Electronics Design Engineer to work for a leading Automotive client of mine based in Surrey. Salary circa and#163;50,000You role will be based around Micro-controller design for Automotive components including Instrument Clusters, displays, body electronics, Multiplexing system components, Engine Management systems.  Requirement for this role are as follows:- 1st or upper 2nd Degree in Electronics or Electronics discipline- At least 4 Years Experience part of which should be within the Automotive industry- The candidate should have solid experience of the full design flow from initial design specification through to component testing and validation.- Core competences must include: analogue design, digital design, use of FPGAand#146;s.Desirable attributes include:- Working with embedded LCD Displays- High speed digital design with knowledge of signal integrity verificationPlease get in touch ASAP should this role be of interest.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Refrigeration Design & Development Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob533789AED0AF8F34482579F5001BA5D2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Refrigeration-Design-and-amp-SHARP38-Development-Engineer_1658610.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Refrigeration Design and#38; Development Engineer and#150; Middlesex - and#163;30-35,000 paThe ClientA leading Manufacturing company of refrigeration systems are looking to grow their team within the Design department and are in need of a Refrigeration Design and#38; Development Engineer. The RoleThe Refrigeration Design and#38; Development Engineer will be working on multiple projects at one time designing cooling systems using SolidWorks.The CandidateStrong Mechanical Design experience within similar industry and#150; Refrigeration, Glycol, Air conditioning systems, cooling systems, chilling systemsHands on technical experience of building prototypes and machiningSolidWorksThe Salaryand#163;30-35k pa How To ApplyIf you would like to apply for this position, please email your current CV and a covering letter to and/or call Lucy Heap on 0118 956 5545 for an immediate response. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR FEA ENGINEER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD988C189484F763F482579F5001BA5E5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-FEA-ENGINEER_1658611.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Senior FEA Engineer and#150; Surrey - and#163;40-55k paThe ClientA Global Engineering company of conductor systems who specialise in the design, analysis and management are looking to recruit for Senior Analyst Engineer to join their growing team based in Surrey. The RoleThe Senior FEA Engineer will be responsible for performing design calculations and analyses of subsea structures. You will need to liaise effectively with other engineers, clients and suppliers. The role may include occasional travel both in the UK and overseas. The CandidateMust have strong FEA Must be degree level educatedMinimum 3 years experience in mechanical and structural analysis in offshore oil and gas industryPreferable experience in risers, flowlines, subsea equipment, water platforms The Salaryand#163;40-55,000 pa How To ApplyIf you would like to apply for this position, please email your current CV and a covering letter to and/or call Lucy Heap on 0118 956 5545 for an immediate response.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR DESIGN ENGINEER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6B81A754FF63DAD7482579F5001BA5F5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-DESIGN-ENGINEER_1658612.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Senior Mechanical Design Engineer and#150; Luton - and#163;32-42,000 paThe Clientand#149;To provide technical leadership in design and development of water meter registersand#149;To prepare and review 3D models for clash detection and operation at extremes of tolerance and temperatureand#149;To supervise junior/temporary staff and#149;To assist in developing test, development and verification plans for registersand#149;To maintain the current register sub-system technical specifications and develop new versions as appropriate The Candidateand#149;Experience of Design and#38; Development of New Product preferably within a high volume manufacturing environment and#149;Experience in design calculations for stress, stiffness and thermal expansionand#149;Good 3D design skillsand#149;A good degree in Mechanical or HND in Mechanical EngineeringThis position would initially take on the key programme management and coordination role leading on to full design leadership.The Salaryand#163;32-42k How To ApplyIf you would like to apply for this position, please email your current CV and a covering letter to and/or call Lucy Heap on 0118 956 5545 for an immediate response.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PCB Design Engineer  Hampshire  Circa £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC376123BDDF17BC7482579F5001BA600</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PCB-Design-Engineer-Hampshire-Circa-and-amp-SHARP16335000_1658613.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently seeking a PCB design Engineer to work for my client based in Hampshire. Salary circa and#163;35,000.Your role will be to design cost effective products using cutting edge technologies for high volume manufacture. You should have high competence design skills in using E-cad software preferably Cadence schematic capture and Cadence PCB editor. You will be generating PCB designs of medium to high complexity, on two to four layered boards. EMC complaint and designed for manufacture. The ideal candidate will have experience in the following areas:-Experience of Cadence schematic capture-Experience of Cadence PCB editor version 16-Experience in the use of 2d drafting (Creo elements and#150; ME10)-Dimensioning and TolerancingAny experience of PCB Design within the Fire and Detection industry or with Fire detection products will be of great benefit. If this is of interested then please get in touch ASAP as it is an immediate requirement.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC7BD8BC8F6C81F94482579F5001BA60F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Engineer_1658614.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Engineer and#150; Berkshire - circa and#163;35,000 Huxley Associates are working with a large multinational organisation in Berkshire to recruit for Project Engineer.Our client operates within the food and beverage industry providing to a global region. They understand that employees are vital to the progression of the company and as such are seen as key assets.Job Details:The key responsibilities are manager engineer lifecycles from initial concept across supporting manufacture to commissioning.ExperienceThe main attributes to be seen on a CV are the following:-Background within the food industry-Experience in a project engineering or project management role and#150; at least 3 years-Degree qualified or equivalent within mechanical or chemicalYou may have experience in the following roles: Project Management, Project Leader, Delivery Project Manager, Project Engineer Salary: circa and#163;35,000  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Unit Manager, Aerospace]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3C6CFE6D80474567482579F5001BA61E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Unit-Manager-Aerospace_1664262.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Dear Gary, I have interview slots for Tuesday 8th and I need some solid Business Unit Managers to apply for a very exciting role. Dont panic if you arent free on the 8th, this is just a benchmark date. Now what I need is somebody who has operations management experience, within the Aerospace Sector and a degree. Youre looking at a potential salary of and#163;60k+. If you would like to know more, me an updated CV  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Test Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE4B806232E3F49C6482579F5001BA62C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Test-Engineer_1664263.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Tasks: Using data from Risk Analysis, FMEA and technical specifications, define and document test protocols for a  Class IIb medical device conforming to appropriate Global Standards.Verify and validate both System and individual components (as required).Will need to work to a deadline both independently and in close coordination with the existing project software and hardware engineers. Day to day responsibilities:- Be working with the Software and Hardware Engineers - Testing the hardware - Developing the Test Specs - Analysing and presenting the test results - Life Testing / functional testing - Designing and making the test jigs - Confirming the supplier specifications - Testing sub assemblies i.e. pump heads / motors - Testing the overall unit / system - Will be involved from components through to sub assemblies and full system - Will be defining test specsExperience:Previous medical experience in class IIb or above would be preferable.Experience of designing test rigs would be advantageous.Use of Solidworks would be an advantage but not essential to the right candidate.Start  and finish:Start is ASAP:Expected minimum contract for 6 months.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Assembly Engineer  West Mids  12 month contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob85C7D1AE759C3546482579F5001BA652</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Assembly-Engineer-West-Mids-12-month-contract_1664268.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[An excellent opportunity has arisen for an Assembly Engineers to work on an interim basis for a world leading Automotive component manufacturer.As the assembly engineer, you will:-Take project drawings and further develop the assembly process-Take products through the process route through suppliers and deliver a final solutionThe job purpose will be to develop the assembly line and establish the process needs. Our client, who are a leading automotive metal components supplier, deal mainly with pressed steel products, Body in White (BIW) and Chassis.As a successful assembly engineer, you will have a background from a First Tier Automotive company and have had exposure to working within a fast-paced assembly line - dealing in the delivery and installation of assembly line, worked with customer documentation and FMEA. Rate commensurate with skill-set and experience Contract length to be a  minimum of 12 months with a view to extend further.Please apply with an up to date version of your CVand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Catia V5 Design Engineer  up to 60 hrs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFDBC003835CB85E0482579F5001BA662</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Catia-V5-Design-Engineer-up-to-60-hrs_1664269.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client are the most diversified automotive supplier in the world. They design, develop and manufacture automotive systems, assemblies, modules and components, and engineer and assemble concept vehicles, primarily for sale to original equipment manufacturers (OEMs) of cars.Due to a major project they have just won with Nissan, Bentley, Lotus and McLaren, they require 3 to 4 Mechanical Design Engineers with experience of using CATIA V5 and exposure to the design of automotive parts on a contract basis for 6 months, possibly longer. To be successful, you will be an experienced Mechanical Design Engineer with experience of using CATIA V5 and exposure to the design of automotive interior parts or car body structures ideally within an automotive OEM or automotive 1st tier / first tier environment. In addition, you will also be required to work closely with the customer, suppliers and the on site manufacturing team, to follow a design through to production. My client is offering up to 60 hours per week.The role will be located within the West Midlands.Hourly rate is negotiable based up on previous experience.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Purchasing Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB49330CB0FDF9884482579F5001BA67D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Purchasing-Manager_1664271.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading design and manufacturing company is currently looking to employ a Technical Purchasing Manager. They are looking for someone to join the purchasing team, and develop Strategic purchasing within the company.The successful candidate will have:Mechanical Engineering background and#150; need to understand engineering processes, engineering suppliers and#38; read engineering drawingsExperience working in or alongside Rand#38;D and NPIStrong supplier work and#150; selecting new suppliers, understanding of RFQ Process and monitoring current suppliersFar East Sourcing ExperiencePurchasing knowledge and#150; purchasing for NPI and#38; current manufacturing requirements, supplier management, contract management and costingExperience with ERP/MRPCIPS is desirable, but not essential The role will involve, but duties are not limited to:Supporting NPIDevelop the purchasing strategy which will create cost downWorking very closely with suppliers: sourcing, selection and#38; developmentPurchasing samples for NPI and#150; most purchasing will be handled via the operational purchasing divisionDeveloping the Strategic Purchasing department to support additional membersThe successful candidate will benefit from a competitive salary If you are interested in applying for this position please attach your CV, including salary expectations, and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solid Works Design Engineer,Wolverhampton, 6 Months, Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2ECF3305E3F1FC64482579F5001BA72D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solid-Works-Design-EngineerWolverhampton-6-Months-Negotiable_1664282.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Solid Works Design Engineer,Wolverhampton, 6 Months, NegotiableMy Wolverhampton based client is currently recruiting for a Solid Works Design Engineer for an initial 3- 6 month contract. Candidates will be involved in the design of belt conveying and bucket elevator systems and heavy container handling equipment using Solid Works and Autocad. My client is a heavy manufacturing company that design and manufacture a wide range of foundry equipment, mechanical handling and bulk materials handling equipment and recycling equipment.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Composite Procurement Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob911BFDB07EBC0D8C482579F5001BA75E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Composite-Procurement-Manager_1664285.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading company in the Automotive sector based in the Thames Valley area to recruit an Interim Procurement Manager with strong Supply Chain skills.  We are looking for someone who has a proven career history as a Supply Chain Manager / Procurement Manager and can bring strong strategic knowledge to reduce costs and manage inventory levels to ensure they can deliver to clients needs.This will be a great role for an experienced candidate who wants to develop and implement procurement strategy, lead strategic sourcing, be involved in pricing and contract negotiation, manage inventory and stock levels to reduce cost, manage and grow supplier relationships and rationalise the supplier base and product lines.     To be considered we want to see you have the skills and experience to lead their Procurement team and bring about cost savings through the introduction of new Supply Chain and Procurement strategies.  It is very likely you will have a proven track record in the F1 Automotive/Composites industry. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Purchasing Manager  912 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9ADECE34345F372C482579F5001BA76B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Purchasing-Manager-9-12-Months_1664286.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading Construction company based in the South East to recruit an Interim Purchasing Manager to join their team for a period of 9-12 months.The main focus of the role is to take more of a consultative approach and look at the current purchasing processes that are being used, and advise and implement a strategic plan in order to become more lean and generate significant cost savings for the company.To be considered you will have experience in;- Change management- Risk assessment- Transformation- Strategic planning and implementation - External supplier management- Internal stakeholder management- Teaching and training would be an advantage- Experience in the Construction Industry would be an advantagePlease send me a copy of your up to date CV and I will call you back to discuss the role in more detail. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Senior Sourcing Manager  North London]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob11A686CFC17F7E85482579F5001BA778</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Senior-Sourcing-Manager-North-London_1664287.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is looking to take on an Interim Senior Sourcing Manager to join the UK division of their worldwide EPC Company. The successful candidate will join the ever growing Purchasing team which is based in North London. The candidate will have:- Project Purchasing experience- Strong negotiation skills- Supplier management skills- Stakeholder management skills- Sub-contract experience- Strong communication skills- Monitoring and reporting progress to board level- Experience in the Rail, Civils or Infrastructure is essential- MCIPS qualified is desiredThe role will include:- Negotiate with existing and new suppliers- Monitor and manage supplier performance- Manage internal stakeholders- Lean practices- Sub-contract ManagementPlease send me your up to date CV and desired daily rate and if you are successful I will call you back to discuss the role in further detail. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB2DCE1B29EE78B3E482579F5001BA787</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Engineer_1664288.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Engineer and#150; Gloucestershire to and#163;35,000A leading niche, luxury-manufacturing company is currently looking to recruit a Project Engineer to add to their successful team. Job Details:The Project Engineers key responsibilities are to project manage (NPI) new product introduction by bringing together all aspects of engineering to successfully deliver the finished product.ExperienceThe main attributes to be seen on a CV are the following:-Experience within a mechanical environment-Project management / project engineering experience from conception to completion-Ideally experience reading technical drawings-Ability to work in a multi-cross functional teamYou may have experience in the following roles: Project Engineer, Project Leader, Senior Project EngineerSalary: to and#163;35,000If this is of interest or you know someone who is looking please forward me a copy of your most recent CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Hardware Engineer  Hampshire  Fantastic Package]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB95768CC54D31F70482579F5001BA795</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Hardware-Engineer-Hampshire-Fantastic-Package_1664289.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for a Hardware Engineer to join a leading problem-solving electronics company based in Hampshire with a fantastic salary and benefits package. You role will be to work within the Research and Development team, innovating, designing, developing and supporting systems and electronics hardware solutions for a variety of standard and bespoke products. Generating documentation for and controlling designs both internally and for external releaseThe ideal candidate will have experience in the following:and#149;Demonstrable design experience of electronics hardware design for embedded systemsand#149;Circuit design to single transistor level for analogue and digital signal processingand#149;Good understanding of mechanical design principles and electronics packagingand#149;EMC and Environmental testingand#149;Use of laboratory equipment (Oscilloscopes, DVMs, signal generators etc)and#149;Proficiency in PADs or other similar ECAD softwareand#149;FPGA based design]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Engineer  Hampshire   Fantastic Package]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob874D58645585E85B482579F5001BA7A6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Engineer-Hampshire-Fantastic-Package_1664290.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for a Software Engineer to join a leading problem-solving electronics company based in Hampshire with a fantastic salary and benefits package.You will be working within the Research and Development team, designing, developing and supporting embedded electronics software solutions for a variety of standard and bespoke products using both high level and assembler based programming languages. Designing, developing and supporting Graphical User Interfaces for the above products.The ideal candidate should have experience in the following:and#149;Demonstrable experience real-time embedded software design in ANSI C and assembly language.and#149;Demonstrable design experience of Windows programming.and#149;System level design using OOD or UML.and#149;Production of documentation including specifications, release of software and user manuals.You should also hold or be able to achieve UK security clearance (SC).]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Manager  Coventry  Medical]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8D9B14F3915C2025482579F5001BA7B1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Manager-and-amp-SHARP150-Coventry-and-amp-SHARP150-Medical_1664291.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is pleased to be working with a leading manufacturer to the Medical industry based in Coventry. An excellent opportunity has come available for a Quality Manager to join their team. This is an opportunity to join a well- known market leader who are going from strength to strength within the industry. Interested? We are looking for some of the best Quality Managers within the industry. Ideally you will be from a medical device or pharmaceutical background but this is not essential- all industry experience will be considered. Most importantly you will need to be a team player as you will be managing a quality team of 3 experienced Quality technicians.  Feel you have what it takes? On offer for the role is a starting salary of circa and#163;45,000 plus bonus and contributory pension. This is an urgent role with shortlisting occurring now so if you would like to be considered please apply online to Brooke Whitehead at Huxley Associates ASAP in order to avoid disappointment.NB May suit individuals with a background as (but not limited to): Quality Manager, Quality Director, Senior Quality Engineer.This role is commutable from: Coventry, Birmingham, Warwickshire, Worcestershire, West Midlands, Leicestershire, Derbyshire, Nottinghamshire, Northamptonshire, East Midlands. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solidworks Engineer Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob922D146844FEB283482579F5001BA7C6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solidworks-Engineer-Bath-and-amp-SHARP16340000_1669769.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a Solidworks engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Siemens WinCCRockwell Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob401A1D5620B7A307482579F5001BA7D4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Siemens-WinCC-Rockwell-Engineer-Bristol_1669770.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a PLC/SCADA software engineers to join a market leading organisation based in Bristol.This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;35,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Automation Engineer Bristol £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC758A97AD8D4005F482579F5001BA7E3</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Automation-Engineer-Bristol-and-amp-SHARP16335000_1669771.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a automation engineers to join a market leading client based in Bristol. This is a fantastic opportunity to work with a very well established client who is in an exciting period of growth creating opportunities for progression. My client produces high level software products for systems integration and control systems for shop floor automation. Essentials: - Siemens WinCC/PCS7 or Rockwell Automation - Strong written capabilities - Willingness to travel to client sites- 20% travel Salary is on offer up to and#163;35,000 + benefits including a pension, starting on 25 days holiday + bank holidays and a flexitime scheme. This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088. The successful candidate may be required to work on one or more projects concurrently as agreed with the Software Engineering Manager. The Software Engineer is responsible for ensuring technical support is provided up to and through the manufacturing and test of the project deliverables. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Business Development Manager Oil and Gas]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC1B00C1960EA6A1E482579F5001BA7EF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Business-Development-Manager-Oil-and-Gas_1669772.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are delighted to be working with the market leader in the supply of pumps for use in the marine, power generation and oil and#38; gas industry markets across the globe. Founded just under 100 years ago they pride themselves on technical innovation. The Company is seeking to expand its presence in global oil and gas markets and is now seeking to appoint a high calibre, industry-experienced sales professional. As Business Development and Account Manager, the job holder will be expected to: -Lead the Oil and#38; Gas industry sales team and have responsibility for sales and account management globally. - Develop, negotiate and agree contract specifications with a variety of external groups, including engineering contractors and end-users. - Be the primary account manager for business in the oil and gas market sectors. - Develop and maintain relationships with the engineers and decision makers within the above organisations and control internal CRM processes. - Develop sales plans and appropriate targets as part of the Divisionand#146;s management team and achieve the necessary orders to fulfil these. - Have involvement in the preparation and generation of quotations - Promote internally the products and customer service necessary to achieve sales plans - Spend a reasonable portion of their time (approximately 40%) as the Companyand#146;s representative in our market areas. Capabilities, experience and education Applicants will be expected to have the following capabilities: - Will have a strong sales background within an engineering environment and preferably in pumps and rotating machinery. - Strong commercial experience and demonstrated skills in customer relations management (CRM). - International sales experience is essential plus knowledge of the culture aspects of selling into a worldwide market. - They must have had exposure to specification selling; they will ideally have a demonstrable track record of success within technical sales. - A degree level education or equivalent experience. - Knowledge of the oil and#38; gas industry arena, and ideally motor and/or pump design and operation. - Capable of demonstrating previous successful performance leading a sales team. The ideal candidate will build on their experience whilst challenging the boundaries of present market coverage with the support of electrical, mechanical and hydraulic design engineers.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Executive NHS & Local Government 90k 0TE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFDB7A4396F1F9372482579F5001BA822</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Executive-NHS-and-amp-SHARP38-Local-Government-90k-0TE_1669774.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to be part of an ambitious and entrepreneurial company who are looking to aggressively grow in size. They now have a requirement for a Sales Execs to join the company. The focus would either be on the NHS or Local Government Ideally you will have experience selling IT Software solutions and have worked in all parts of the sales process including Account Management and Business Development. Experience with selling CRM systems would also be beneficialThe company are looking to make an Initial Public Offering within the next 5 years and this role offers the candidate the opportunity to get involved with equity participation and eventual company directorship. The role would require the candidate to be based from Woking and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Production Planner]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6EEB71B794B6A0C0482579F5001BA82F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Production-Planner_1669775.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Production Planner and#150; Hampshire Huxley Associates are working with a leading precision manufacturing company based in Hampshire to recruit for a Master Scheduler / production planner. Job Details:The main purpose of the role is to champion production planning as lead master schedulerExperience:The main attributes to be seen on a CV are the following:and#149;Proven Experience as a Master Scheduler / production plannerand#149;Background within the manufacturing industryand#149;Ideally experience within a precision engineering environment but not essential.Salary: NegotiableIf this is of interest or you know someone who is looking please forward me a copy of your most recent CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[UK Sales Manager  Software Sales]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE32ACCB40E588F34482579F5001BA841</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/UK-Sales-Manager-Software-Sales_1669776.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[UK Sales Manager opportunity East Midlands and#163;50,000, + Bonus + Pension + Health Care Interviews; Week commencing 7th/14th May  My services have recently been required by a leading clean energy and transportation consultancy who have site locations globally. The company have developed groundbreaking technology, and with a clear path for progression and continued growth, this is a great company to join which can offer career progression to candidates who demonstrate the ability to work at a senior level. They have very specific growth plans this year are looking to grow 40% this year alone! As a result they are seeking sales driven/ commercial professionals who want to contribute towards this. The successful candidate will be reporting to the Commercial Director, and will be challenged with a number of tasks across the business in order to make improvements to their services. Tasks will include, sales planning for the UK Business, managing and developing existing UK Accounts whilst achieving annual/ quarterly targets. This position will enable the successful candidate to build a solid platform and understanding of the business allowing for career succession in a business that has planned/forecast growth. This vacancy has so much potential, the ideal candidate will relish a challenge and be willing to earn their stripes in an international company. To be considered for this position you must be degree qualified, and have a history working for reputable companies for periods of time that demonstrate your commitment. Software sales experience is essential preferably with ANSYS, Matlab, Simulink or Catia. Automotive, marine, rail or aerospace experience is essential, preferably with OEMs. Product experience of gearboxes, driveline or bearings would be desirable. Project/ Account Management skills are also essential. They are looking for someone who is Dynamic, a candidate that has a real ability to represent the company in the very best light, whether that is to customers or to members of the team including senior management. If you think you have the potential to assume this position. Provide yourself with the opportunity of generating an interview by forwarding me your CV.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[M&E Planner  London  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F851380112E37C7482579F5001BA84E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/M-and-amp-SHARP38E-Planner-London-Contract_1669777.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am looking for a Planner with building services experience to work in London. Candidates must have experience using ASTA Power and have a  mechanical and electrical background.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  URGENT  CONTRACT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob56B186DEB38C66A2482579F5001BA85E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-URGENT-CONTRACT_1669778.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Salisbury and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team in providing them with analysis for a number of new and existing products in their existing range for the Oil and Gas industry. Analysis is needed to bring their products up to BS EN 60812 qualification.Essential Skills:and#149;Experience with Autodesk Inventorand#149;AUTOCAD 2Dand#149;Stress Calculationsand#149;Hand calculationsand#149;Failure mode analysisDesirable Skills:and#149;Previous experience within the Oil and Gas Exploration industryand#149;Experience with hydraulics, piping instrument diagramsand#149;Working on a BS EN 60812 project beforeRate: MarketLocation: SalisburyDuration: 3 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Field Service Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob22CD23DC9D26869B482579F5001BA868</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Field-Service-Engineer_1669779.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[RF Engineer and#150; Hampshire and#150; and#163;25,000 + BONUSES (Second year ote and#163;30,000-and#163;32,000) Huxley Associates are working with a leading organisation based in Hampshire to recruit for a field based RF engineer. They understand that employees are vital to the progression of the company and as such are seen as key assets. Job Details: The main purpose of the role is to fault find and repair company equipment for clients on site Experience The main attributes to be seen on a CV are the following: - Experience as a field based engineer - Ideally experience as a RF Engineer - Experienced fault finding within electrical or mechanical - Competent customer facing experience - Willingness to travel - Strong initiative You may have experience in the following roles: RF Engineer, field service engineer Salary: and#163;25,000 + BONUSES (Second year ote and#163;30,000-and#163;32,000)  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Client Director  Central Government 100k OTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA5084F5841721DE0482579F5001BA877</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Client-Director-Central-Government-100k-OTE_1669780.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to work for a Not for Profit organisation who have grown by 20% year on year since they were established. Providing Cloud and IT Services to the Public Sector my client has ambitious plans for future growth. Due to this growth they now have an excellent opportunity for a Client Director to look after one of there largest Government Accounts Reporting to the Business Development Director the role will be to further grow the Provision of Web services and hosting in addition to Cloud based services. You will be maintaining C Level,Director Level and Operational Level relationships within this Account. Looking for ways of growing the business/income opportunities within this key account is vital. You will also be responsible for developing the Account Strategy for this client. You will ideally have a proven track record in Consultative selling of IT Services/Application Development or Business Consultancy., with a proven track record in managing large Central Government Accounts A technical or Pre Sales background would also be desirable. Experience of the Education sector would also be desirable. Degree Educated would also be desirable This is an excellent opportunity to join a rapidly growing organisation who also offer a Final Salary Pension scheme. The ideally candidate will either be based in the South East or South West. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Business Manager  Central Gov Sales 100k OTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC799BE93E413331D482579F5001BA88F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Business-Manager-Central-Gov-Sales-100k-OTE_1669781.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to work for a Not for Profit organisation who have grown by 20% year on year since they were established. Providing Cloud and IT Services to the Public Sector my client has ambitious plans for future growth. Due to this growth they now have an excellent opportunity for a New Business Manager to source new opportunities within Central and Local Government.  Reporting to the Business Development Director the role will be to further grow the Provision of Web services and hosting in addition to Cloud based services. Responsibilities: Leading the company sales strategy for Central and#38; Local Government Leading the identification of new sales opportunities in Government Owning the relationship with existing and new Government clients Your Experience: Experience of securing new business with Government or Public Sector clients Ability maintain strong relationships with clients Successful track record in Consultative selling of IT Services and Solutions Proven track record of exceeding Sales Targets This really is an excellent opportunity to grow a rapidly expanding company who also offer a Final Salary Pension scheme. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobABDDC162CD8CD1D0482579F5001BA899</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Engineer_1669782.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Manager and Project Engineer Opportunities and#150; Berkshire Head office Huxley Associates are working with a leading civil engineering organisation who specialise within the water/ waste water industry. They are looking to increase turnover by 50% over the next 2 years following a recent acquisition. They understand that employees are vital to the progression of the company and as such are seen as key assets.Job Details:The key responsibilities are to run Civil Engineering projects for the key clients.The main attributes to be seen on a CV are the following:-Experienced within  Civil Engineering -Experienced with water/wastewater projects-Experience within a Project Engineering/Management role-Possess business acumen and commercial awareness -Ability to motivate and lead an engineering teamYou may have experience in the following roles: Project Manager, Project Leader, Project Engineer, programme manager, programme leaderSalary: Competitive and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Valves  Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0A05C1CC3C402973482579F5001BA8AA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Valves-Bristol_1669783.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month rolling contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;Subsea experienceand#149;Subsea sensing equipmentand#149;Control Valvesand#149;Subsea Structuresand#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerRate: MarketLocation: BristolSTATUS: URGENT and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Valves  Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDF4DBA5A7DDD2A21482579F5001BA8C0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Valves-Bristol_1669784.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Salisbury and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team in providing them with analysis for a number of new and existing products in their existing range for the Oil and Gas industry. Analysis is needed to bring their products up to BS EN 60812 qualification.Essential Skills:and#149;Experience with Autodesk Inventorand#149;AUTOCAD 2Dand#149;Stress Calculationsand#149;Hand calculationsand#149;Failure mode analysisDesirable Skills:and#149;Previous experience within the Oil and Gas Exploration industryand#149;Experience with hydraulics, piping instrument diagramsand#149;Working on a BS EN 60812 project beforeRate: MarketLocation: SalisburyDuration: 3 Months with the possibility of an extension and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Export Sales Manager  Utilities  Meters]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA7632A4C0448505E482579F5001BA8F8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Export-Sales-Manager-Utilities-Meters_1669787.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Export Sales Manager. Working with a leading Meter manufacturer based in the UK.You will have a proven background of high value export sales selling technical products such as data loggers or meters.Key Skills:International export sales experience, ideally within a utilities related market* Commercial competence with experience of negotiating at a high level* Comprehensive commercial skills.* A sufficient technical background  - Metering and#38; data loggersA qualification in  Engineering would be beneficial, as well as additional languages and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4431CCF9AA25BF66482579F5001BA908</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer_1669788.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A Key client of ours is seeking two HV Electrical Design Engineers as well as one with LV experience. This is due to rapid growth having taken over a new site ca. 2 years ago, and following 3 new positions have been created to supplementing the Water and Gas design capabilities already in place.The company offers an excellent benefits package and invest heavily in their staffs development including specific training linked to your role, and lastly support a philosophy of giving their Design Engineers a lot of exposure to clients to understand their needs. It therefore becomes a more varied role including design, customer liaison, and assisting quotations.Electrical Design Engineer - HV (high voltage) and LV (low voltage) - ManchesterSeparate HV and LV roles.ROLEDevise, cost, quote and win single and multi-utility contestable connections and contracting projects and#150; including Wind grid connection, Generator connections, Private Networks and Primary Substation projects. -Prepare 33/132kV electrical designs and quotations for contestable utility and contracting projects.- Ensure that designs are fully compliant with host utility specifications.- Incorporate customer requirements and advise on loading profiles, design layout and delivery lead times.- Contribute to zero accident culture by ensuring that designs comply with safety legislation, including CDM regulations.- Ensure provision of all necessary consents and associated drawings.- Plan, organise and agree your own portfolio of quotations, site visits, customer visits.- Ensure all quotations are submitted strictly in accordance with an agreed customer date.- Ensure fully costed and compliant designs are handed over in a timely way to the relevant Project Manager or Construction Engineer.- Be responsible for managing and reporting enquiries and progress log.- Continue to support the delivery team throughout the life of a project, particularly in the event of significant variations or the need for re-design. YOU - Market and#38; pricing knowledge relating to 33/132kV electrical utility networks.- Supplier knowledge and understanding of procurement best practice and governance.- Technical/safety relating to 33/132kV electrical utility networks and construction generally.- Relevant electricity DNO Specifications, Codes of Practice and#38; Procedures.- Basic understanding of contract law and impact on own activities with regard to approach to risks.- Market and#38; pricing knowledge relating to electrical utility networks.- Minimum HNC in related discipline -Degree preferred.- Experience in sales or key account management an advantage.They WILL consider people without the DNO/District Network Operator experience, but you must have a strong HV background with extensive experience.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Valves  Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD0DFFA8E6E4111BB482579F5001BA91D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Valves-Bristol_1669789.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month rolling contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;Subsea experienceand#149;Subsea sensing equipmentand#149;Control Valvesand#149;Subsea Structuresand#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerRate: MarketLocation: BristolSTATUS: URGENT and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Inspector CMM Operator West Yorkshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8C53968017C02AA6482579F5001BA938</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Inspector-CMM-Operator-West-Yorkshire_1669790.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is currently recruiting for a Quality Inspector who has experience working as a CMM operator. The position is based with a manufacturing client in West Yorkshire and is available on an initial 6 month contract.The successful candidate will have a track record of quality inspection and will be tasked with providing audit inspection services to the project management and quality teams.The successful candidate will also have CMM operating experience working on the Mitutoyo COSMOS (MCOSMOS) software programme.We are able to offer an immediate start to the successful candidate with interviews scheduled to take place after the bank holidays. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Bristol  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9FECBD86E50DFE96482579F5001BA945</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bristol-URGENT_1669791.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month rolling contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;Subsea experienceand#149;Subsea sensing equipmentand#149;Control Valvesand#149;Subsea Structuresand#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerRate: MarketLocation: BristolSTATUS: URGENT and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Bristol  3 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob46035593FAB2C603482579F5001BA956</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bristol-3-Months_1669792.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Bristol  - 3 Month ContractHuxley associates are currently looking for a Mechanical Design Engineer on 3 month rolling contract.The role has come about to assist the design team with a number of new products to their existing range.Essential Skills:and#149;HNC / Degree / Or 5 Years experience working as a Mechanical Design Engineerand#149;Mechanical / Hydraulics experience is essentialand#149;Experience with AUTOCADand#149;Experience with Pro EngineerDesirable:and#149;Subsea experienceand#149;Subsea sensing equipmentand#149;Control Valvesand#149;Subsea StructuresRate: MarketLocation: BristolThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Please send your CV in for immediate consideration. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Engineer   Up to 45k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE9F00C2A89AF1763482579F5001BA965</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Engineer-and-amp-SHARP150-Up-to-45k_1669793.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Award wining Huxley Associates are proud to be working exclusively with one of UKand#146;s leading UPS manufacturers. Part of an international group they are a specialist in the design and manufacture of high power UPS systems. This company have established themselves as a market leader not only throughout the UK but on a global front. Due to internal promotion and a restructure in their sales team they now have 2 vacancies in their sales team. Working from home and reporting to the senior management team you will be selling to contractors and consultants predominantly in the London region focussing on the data centre and financial markets. This will be project based sales so typical gestation periods will be anywhere from 6 months to 3 years with order values typical in the region of and#163;2-4 million. It is therefore essential that you are used to this type of solution based sell and have a strong technical grasp of the product.  Key responsibilities will include:and#149;Search and prospect for new clients and develop existing client baseand#149;Travel to visit potential clients and provide technical site/installation/product based supportand#149;Preparing client quotations and proposalsand#149;Negotiating tender and contract termsand#149;Preparing sales and forecast reports on a regular basisMinimum requirements for the role are:and#149;Proven track record of technical sales and#150; within UPS, generators or switchgearand#149;Experience selling to consultant engineers and contractorsand#149;Experience in handling high value Mand#38;E contracts.and#149;Used to a long term, solution selland#149;Ability to negotiate commercial contracts.and#149;Proven relationship building skillsIn return you can expect a salary somewhere in the region of and#163;45k-and#163;50k with bonus, car, pension and healthcare on top. So if you are interested in taking your career that one step further and want to work for a dynamic and forward thinking organisation, please apply nowand#133;and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Master Scheduler]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCCD21BC1AF976F24482579F5001BA973</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Master-Scheduler_1669794.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Master Scheduler and#150; Hampshire Huxley Associates are working with a leading precision manufacturing company based in Hampshire to recruit for a Master Scheduler. Job Details:The main purpose of the role is to champion production planning as lead master schedulerExperience:The main attributes to be seen on a CV are the following:-Proven Experience as a Master Scheduler-Background within the manufacturing industry-Ideally experience within a precision engineering environment but not essential.Salary: NegotiableIf this is of interest or you know someone who is looking please forward me a copy of your most recent CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Unigraphics NX Design Engineer, Staffordshire, Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD0F08974BA36BA8D482579F5001BA981</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Unigraphics-NX-Design-Engineer-Staffordshire-Negotiable_1669795.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Unigraphics NX Design Engineer, Staffordshire, NegotiableMy Staffordshire based client is currently recruiting for an NX Design Engineer for a 6-12 month contract. They are looking for candidates who are skilled in the use of NX and have experience in the design of armoured or off road vehicles, hydraulics, engine installation, yellow goods. This is an immediate requirement and interviews will be happening next week.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Category Buyer  Guildford  12 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob684663558A58C1EA482579F5001BA98E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Category-Buyer-Guildford-12-Months_1669796.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client, a leading Manufacturing organisation based in Guildford with an excellent reputation, now requires a Senior Category Buyer to join them at the earliest opportunity.The successful candidate will be expected to lead on the procurement divisionand#146;s approach to managing and delivering successful regional procurement in identified key sub-categories, especially the complex / high value procurements (which will involve the full engagement of key stakeholders) and building effective and productive relationships with specific suppliers, as well as leading a procurement team.Key Accountabilities: Regional Development and ManagementCategory StrategyCategory SourcingCategory Management The successful candidate will have:and#149;Proven capability in business requirements/supply market analysisand#149;Proven procurement ability, ideally in category management with a sound knowledge of Public Procurement Law (OJEU)and#149;Excellent negotiating and influencing skillsand#149;Demonstrably capable of effective stakeholder and supplier managementand#149;Experience of working in a multi-organisational partnershipand#149;Financial / commercial awarenessand#149;Proven planning and organising skillsand#149;IT skillsand#149;Ability to work under pressure delivering a complex and demanding workloadand#149;Ability to work within strict timescales and deadlinesand#149;Ability to deliver results using own initiative, with minimal direct hands-on supervisionand#149;Graduate Level CIPS qualification (MCIPS), a Business Qualification e.g. MBA, or significant commercial experience with a proven track record of success in a similar discipline (Desirable).If you are interested in this role please send me your up to date CV and if you are successful I will call you back to discuss the role further. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Commerciele Process Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEE047C2501804326482579F5001BA99A</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Commerciele-Process-Engineer_1669797.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Commerciele Process EngineerBranche: Chemie (Plastic/Polymeer)Salaris: 50-70kLocatie: LimburgFulltimeVoor een internationale chemische speler in Limburg is Huxley Associates urgent op zoek naar een commerciele process engineer.Taken en verantwoordelijkheden:- Je draagt zorg voor de benchmark van het productieproces tegen processen van de concurrentie - Je analyseert (zowel in -als externs) mogelijke verbeteringen (inclusief uitbreidingen) van het productieproces- Je ontwikkelt nieuwe markttoepassingen van business concept naar commercieel succes.- Je ontwikkelt en implementeert de wereldwijde verkoop strategie voor de markt - Je ontwikkelt het jaarlijkse begrotingsplan- Je bezoekt klanten wereldwijdProfiel:- HBO/WO werk -en denkniveau richting chemie - Minimaal 3 jaar ervaring in de procesindustrie (plastic/polymeer is een pre)- Kennis van plastic/polymeren- Ervaring op het gebied van B2B (e.g. vaktechnische vragen van klanten)Interesse? Reageer dan nu ter attentie van Daniel de Keyzer van Huxley Associates via dde onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SHE Manager (HVK of MoSHE)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob55F5388544F36F67482579F5001BA9AA</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SHE-Manager-HVK-of-MoSHE_1669798.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: SHE Manager (HVK of MoSHE)Branche: Petrochemie - OnshoreSalaris: 90-140kFulltimeBereid 95% internationaal te reizen; langdurige projecten in het buitenlandVoor een petrochemisch bedrijf is Huxley Associates urgent op zoek naar een Safety Manager (HVK of MoSHE). Deze functie zal gepaard gaan met 95% internationaal reizen.Taken en verantwoordelijkheden:- Je bent verantwoordelijk voor de veiligheidheid in het bedrijf.- Je bent verantwoordelijk voor de algehele veiligheid van site projecten.- Je draagt zorgt voor de Veiligheid en Kwaliteit afdeling (20 medewerkers)- Je implementeert het OHSAS 18001-veiligheidssysteem (in combinatie met het betrokken personeel).- Je reviewed en implementeert het project Veiligheid Plan (JSAs - TRAs etc) en zorgt ervoor dat het veiligheidsmanagementsysteem is in overeenstemming met de opdrachtgever en Contract vereiste.- Je begeleidt en technische ondersteunt het personeel ter voorbereiding van het veiligheisplan. - Je zorgt ervoor dat de Veiligheidsrecords en statistieken in overeenstemming zijn met de ISO-eisen.- Je controleert en voert Safety Training programmas uitProfiel- HVK of MoSHE diploma- Minimaal 8 jaar ervaring met veiligheid in de petrochemie.- Minimaal 5 jaar ervaring met de veiligheid op managementniveau.- Lid van Professional Institute (pre).- Werkervaring met ISO 9001-2000 systemen en OSHAS 18001Interesse? Stuur je CV naar Daniel de Keyzer van Huxley Associates via de onderstaande linkand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Desing Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob52FC08AB4148E259482579F5001BA9BA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Desing-Engineer_1669799.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design/Project Engineer - SCADA/PLC - Energy / Oil and#38; Gas - South Yorkshire - PermanentA rapidly growing client of ours require Design/Project Engineers, due to continued growth, and secure prospects from clients. This will allow the Client to take on additional projects providing several years worth of work.CompanyThe UK office in South Yorkshire employs around 30 people, including existing Design/Project Engineers. The engineering side of the business had been split into Two groups, who will still be sharing engineers across the two. They are headed up by Business Group Managers; one for Power and Renewable Clients, and the second for Offshore clients, mainly North Sea Oil and Gas clients.Competitors include Cougar Automation and SCS Controls amongst other.The company design and supply bespoke control system development for clients as well as maintenance services - Integrated Process Central Electrical and Information Management Systems.  Clients include the likes of Veolia and Infinis with small scale generation plant destined for the grid, as well as North Sea oil and gas companies.Project values vary drastically and go up to 3million.Unique Selling Points of Company/Role Variety of the role as goes across the two business units.Follow project from start to finish and#150; concept, design, development, testing, delivery to site, possible maintenance.Heavy investment in the South Yorkshire site Proven growth track record, and excellent future prospects with secure clients.Safety training if choose to go offshoreHigh staff retention.RoleYou will report into a Business group Manager and#150; dependent on where you fit into the business. Based in the South Yorkshire office with an average of 15% travel to site. Travel general comes in blocks throughout the year, and a desire to work offshore for short periods of time would also be beneficial.A Senior candidate would be the main point of contact for the client.YOU- Will have controls and instrumentation experience either from a PLC (programming), SCADA system (configuration - Allan Bradley/Siemens etc) or electrical panel instrumentation perspective. - This should be from a safety critical industry such as Oil and Gas or Energy ideally.- An attitude of being willing to learn, adapt, keen on industry and being a team player.Essential:- Control systems- PLC and#38; SCADAIdeal:- Triconex (triple redundant PLC system for oil and gas safety systems)- TUV certification (safety validation body)- Offshore experienceYou need to have a minimum of a HND with matching experience, and ideally a relevant Degree.  Laslty a work of advise; If you are from a Client environment then the client is very doubtful it would work, as its too different an environment. Look forward to hearing from you.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[BDM  BDD  Industrial Automation, Control Systems]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3108D3AB08D2634C482579F5001BA9D4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/BDM-BDD-Industrial-Automation-Control-Systems_1669800.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Business Development Manager / Director DesignateIndustrial Automation, Control Systems, SCADA, Drives and#38; PLC SystemsAutomotive, Body and#38; White, LogisticsCompetitive Salary and packageAn excellent opportunity has for a Business Development Manager or a Business Development Director to join a world leader in industrial automation and control systems, including SCADA, Drives systems and PLC systems.They are now seeking to expand their business into the automotive sector where they do not have as much presence historically. This is a fantastic opportunity for a Business Development Manager who has sold industrial control systems into the automotive industry. They are also open to taken on a more senior candidate maybe at Business Development Director who is hands on and has the ability to grow a team in the future.  So this is an excellent opportunity for either a Business Development Manager or a Business Development Director with relevant experience selling into the automotive sector. Location is flexible but you will report to a Midlands based facility when required. Salary is dependant upon experience and level of seniority but it will be attractive in order to attract the right candidate.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Supply Chain Planner  612 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6A5A60278905766D482579F5001BA9E8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Supply-Chain-Planner-6-12-Months_1638487.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our Client have an outstanding opportunity for an experienced, entrepreneurial, and forward thinking Supply Chain Planner. Working with a tight knit team, you will have excellent experience of working in a Materials Management/Supply Chain environment. This role will be based in Hemel Hempstead and operating on a 40 hour week.The key responsibilities include but are not limited to the following:* Build, manage and own relationships with a diverse mix of worldwide suppliers to deliver optimal performance and adherence to commitments* To obtain, maintain and follow up on delivery commitments on a daily basis to improve customer satisfaction.* Daily production and#38; monitoring of metrics. Manipulate and#38; analyse data to drive corrective actions to conclusion * Identifying and solving problems within the whole supply chain - such as Warehousing, Hauliers and Purchasing across the business You should have the following: * Business related Degree or equivalent qualification* Experience within Materials Management/Supply Chain environment* Familiarisation and understanding of the complete supply chain (supplier to end customer)* Shown Initiative to identify and rectify supply chain deficiencies * Ability to build working business relationships* Presentations to leadership* European language advantageous * Full UK Driving license [Travel will be required]* Proven Performance improvements on individual and team KPIs to drive forward customer service* SAP/MLE experience - an advantage but not essentialand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Material Planning Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDA22DB99D82E3BE6482579F5001BA9F2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Material-Planning-Manager_1638488.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Hitchin is currently looking to hire a Planning and Logistics Manager You will be responsible for the flow of materials in and out of the business, ensuring that the Master Production Schedule is constantly supported. The successful candidate will have:Significant experience in a similar role in manufacturing or logisticsDetailed MRP experience (MPG pro desirable)Experience with SIOP (Sand#38;OP)Managed 3PLsExperience managing large and diverse teams, and be looking to further your career within this type of environmentThe successful applicant will:Be responsible for all material movement and stock levelsBe responsible for line management of several team leaders within this functionCreate and control the master schedule for all manufactured productsCoach and support value stream plannersEffectively manage suppliersEffectively manage the dispatch of finished goods to achieve on time delivery and minimise transport costs The successful candidate will benefit from a competitive salary and good package, and the chance to join a highly successful and expanding business. If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solid Edge Design Engineer, Derbyshire, 6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDB182A611B49010D482579F5001BAA02</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solid-Edge-Design-Engineer-Derbyshire-6-Months_1638489.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Solid Edge Design Engineer, Derbyshire, 6 MonthsMy Derbyshire based client is currently recruiting for a Solid Edge Design Engineer to assist with Design on a contract basis. Ideal candidates will have a knowledge of the Oil and#38; Gas or Water Industries. They will be proficient in the use of Solid Edge and be experienced in the design of Piping, including; flange pipes, ASME codes, and pressure ratings.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer Company trebling revenue!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE5570A22AF24E538482579F5001BAA13</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-Company-trebling-revenue_1638490.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is proud to be working exclusively with a global Automotive manufacturer based in the Derbyshire area. This a well- respected, leading business who has just won projects which will treble their revenue from and#163;4.5 million to and#163;13 million so this is an extremely exciting time to join the company. Would you like to be part of this success storey? Due to the new projects the company requires a new Quality Engineer on their team. This will be a key role in the business working for an already strong Quality team. We are looking for a strong Quality Engineer with good quality systems experience ideally of ISO9001 and/ or TS16949. You should also have a good understanding of NPI and a good all round Quality toolbox including PPAP, APQP, MSA and SPC. On offer for this role is a starting salary of circa and#163;32,000 which is flexible depending on the successful candidates skills and experience. It is also the chance to join a company at a very exciting time of growth which will offer exceptional opportunity and career progression for the right candidate. This is an urgent position with shortlisting occurring now so if you would like to be considered please apply online to Brooke Whitehead at Huxley Associates ASAP in order to avoid disappointment. NB This role may be suitable for, but is not limited to, the following job titles: Quality Engineer, Senior Quality Engineer, Quality Manager, Quality Inspector. This role is commutable from: Derbyshire, Nottinghamshire, Nottingham, Derby, Staffordshire, Birmingham, Leicestershire, East Midlands, West Midlands.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CAD Technician, 12 Months, Staffordshire 2022hour]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFF2F294C8A26CE1D482579F5001BAA22</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CAD-Technician-12-Months-Staffordshire-20-22-hour_1638491.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[CAD Technician, 12 Months, Staffordshire 20-22/hourMy Staffordshire based client is currently recruiting a 12 month contract for an NX Cad Technician. Ideal candidates will have up-to date knowledge of NX 7.5 and Teamcentre (not essential). Candidates will be involved in the draughting of various components for Off Road Vehicles. They will be required to have a knowledge of BOM creation.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regional Sales Manager  UPS  NorthScotland]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob314E215F68A3D0A6482579F5001BAA2F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regional-Sales-Manager-and-amp-SHARP150-UPS-and-amp-SHARP150-North-Scotland_1638492.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Regional Sales Manager and#150; UPS and#150; North/Scotland Regional SalesUPSNorth/Scotland and#163;45k+If you have proven track record within the power distribution/protection industry and are in the market for an exciting and challenging new role, then please read onand#133;My client is one of the Worlds leading independent manufacturers of specialist power distribution products and due to a replacement; they find themselves looking for a regional Sales Manager to cover the North of England. Turning over more than and#163;300m globally and having operations in more than 50 countries they are a true leader in the field. Experts in protection and switching solutions, they have a large product portfolio UPS protection systems, energy management systems and enclosures and cabinets. They are an extremely innovative company constantly launching new products and setting new standards in the industry. Working from home you will be responsible for the entire Northern and Scotland region calling on End Users, Consultants and Contractors within the Data Centers, Medical and Industrial market. Duties and responsibilities will be to support the current client base in the region as well as exploring potential new business in the region for all the companyand#146;s USP products. You will ideally be HNC/HND Electrically qualified but you must have at least 3 years of successful sales within power protection/distribution or allied industry. My client would look at candidates from the following areas; switchgear, UPS, fuses, metering, MCC, circuit breakers, drives, PLC etc. What is very important is that you are extremely target driven and have the hunger to go that extra mile to win the business. In return you can expect a salary in the region of and#163;45-55k plus bonus and car and be able to take pride in working for one of the key players in the industry. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  APQP  Derbyshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7EB84538DE839AD3482579F5001BAA43</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-APQP-Derbyshire_1638494.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A Derbyshire based supplier to the Automotive industry are urgently seeking a Quality Engineer to join their team, initially on a 3 month basis with a strong possibility of longer term.We are seeking people with the following skills and experience:-A background within the Automotive sector and experience of working within a JIT environment.-Extensive Quality experience and knowledge of Quality tools including APQP.-Experience within an electronics environment would be advantageous but is not essential.This is an urgent role suitable for people who are available at short or immediate notice.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCDB53911AEF71F14482579F5001BAA8D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Contract_1638498.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client are Oil and#38; Gas and Marine specialist based in London and due to new product development they are looking for additional support in the form of two mechanical designers Ideally you will have the following experience:Advanced working knowledge of AutoCAD 2D version 2010, Inventor 3D and a plus would be Solidworks.Knowledge of Microsoft Office applications Outlook, Word, Excel etc. Ability to interpret engineering drawings.Ability to develop concept designs to detailed design stage.Design skills, the ability to think and conceptualise in three dimensions. Demonstrate sound knowledge of mechanical analysis and design software.Experience of participating in teams of structural engineers and designersHydraulic Design experience.Relevant experience, preferably in the offshore oil and#38; gas industry.Installation and commissioning experience.The initial contract is for six months and this role has the potential to be very long term with excellent chances for extension.The rate on offer will depend on your experiences and skills.If the London location is not ideal then there is also a strong possibility to work out of the Portsmouth officeIf this role is of interest then please call me today.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer Exeter]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8ADC0F418567A152482579F5001BAAB6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Exeter_1638501.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Exeter area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? - Proven Mechanical Design Engineer- Solidworks - Preferably a degree in Product or Engineering DesignFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Steel works Bristol £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob44A8CB66A3B73B94482579F5001BAAC1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Steel-works-Bristol-and-amp-SHARP16340000_1638502.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focusses on designing, manufacturing and selling specialist products for the construction/ building services industry.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Steel/ Welding, Fabrication backgroundand#149;                     3D CAD, preferably Solidworksand#149;                     A design or engineering qualificationand#149;                     Creative thinking and problem solvingSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  My client is looking for an innovative, creative and bright engineer that will be involved solely with new product design. The right candidate will have to be creative in order to create concepts for new products as well as being involved with design right through to production.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Aerospace Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob95E4A81E21E3781A482579F5001BAACF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Aerospace-Engineer-Bristol_1638503.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Aerospace Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? - Proven Mechanical Design Engineer - Catia V5 Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Bath]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9201331A6AEBDE8C482579F5001BAADC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bath_1638504.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting, new opportunity in Bath for a Mechanical Design Engineer to join a highly regarded engineering company who are one of the most established companies involved in materials handling.If you would consider a new opportunity and you would be interested to work in this role, please apply here. Full job description is available upon request.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer, PCB  Bristol  £50,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob577622E7EA3DCC55482579F5001BAAEA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-PCB-and-amp-SHARP150-Bristol-and-amp-SHARP16350000_1638505.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Engineer needed - (excellent working environment and#150; successful, cutting edge team) I have an urgent role that has just come on to my books for a growing business that is looking to build their team with and bring in an experienced Mechanical Engineer to lead the team on new development of Switch-mode power supplies. This business has gone from strength to strength and they are market leaders in their industry in which they provide cutting-edge, scientific software solutions. Key Skills: 3D CAD DesignKnowledge of PCB LayoutA good knowledge of the electronics manufacturing processesA degree in mechanical design engineering would be highly beneficialSalary is on offer upto and#163;50,000If you are interested in this exciting role please send your updated CV to me or call Varinder Kandola on 0117 9388088.  The senior design engineer will work within a team of electronics design engineers in driving down complexity and manufacturing costs of new products and technologies and will be responsible for creating PCBand#146;s, moulded parts, sheet metal and enclosure drawings.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer RefridgerationHeating]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob728B9E777AAE0483482579F5001BAAF8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Refridgeration-Heating_1638506.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? -Experience of working within heating/refridgeration industry-Mechanical experience/backgroundFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ElectroMechanical Engineer  Bristol  £50,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4FB6CED9F3F0EDA9482579F5001BAB05</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Engineer-and-amp-SHARP150-Bristol-and-amp-SHARP16350000_1638507.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Electro-Mechanical Engineer needed - (excellent working environment and#150; successful, cutting edge team) I have an urgent role that has just come on to my books for a growing business that is looking to build their team with and bring in an experienced Mechanical Engineer to lead the team on new development of Switch-mode power supplies. This business has gone from strength to strength and they are market leaders in their industry in which they provide cutting-edge, scientific software solutions. Key Skills: 3D CAD DesignKnowledge of PCB LayoutA good knowledge of the electronics manufacturing processesA degree in mechanical design engineering would be highly beneficialSalary is on offer upto and#163;50,000If you are interested in this exciting role please send your updated CV to me or call Varinder Kandola on 0117 9388088.  The senior design engineer will work within a team of electronics design engineers in driving down complexity and manufacturing costs of new products and technologies and will be responsible for creating PCBand#146;s, moulded parts, sheet metal and enclosure drawings.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Bath]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDE4D64231BC7E0F4482579F5001BAB11</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bath_1638508.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bath area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? - Proven Mechanical Design Engineer- Solidworks - Preferably a degree in Product or Engineering DesignFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Bath]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEFFAAFA8742C451D482579F5001BAB21</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Bath_1638510.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bath area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? - Proven Mechanical Design Engineer- Solidworks - Preferably a degree in Product or Engineering DesignFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ISO14001,TS16949  Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBCB6DE8AC621C254482579F5001BAB2F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ISO14001TS16949-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638511.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Assurance and#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Renewables engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob285BF7410B7DEE8E482579F5001BAB3E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Renewables-engineer-Bristol_1638512.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focuses on designing and developing products for the renewable energy market.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Wind Turbine Experienceand#149;                     Offshore Structural ExperienceSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer (catia v5)  £2530hr]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB62B862E52509BC3482579F5001BAB55</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-catia-v5-and-amp-SHARP16325-30-hr_1638514.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client based in the Midlands has an immediate requirement for a Mechanical Design Engineer.Ideally the candidate will have previous experience within an Automotive Industry and familiar with Jaguar Landrover Processes.Primary responsibilities:and#149;Conducts CAD engineering vehicle package studies and analysesand#149;Documents the package issues in an issues tracker and tracks the progressand#149;Organizes a package reviews to get package issues resolutions. Logs the progress in Meeting minutesand#149;Makes design studies and Proposalsand#149;Analyses the Commodities Data for collisions and package issues. Logs the progress in Meeting minutes Skills:and#149;CAD Knowledge: C3PNG/Catia V5, C3PClassic/IDEAS, TCe (team centre) and TDMand#149;Able for Teamwork and Knowledge of CAD environmentsand#149;EDP knowledge (Microsoft office etc.)and#149;English language The contract will run for a duration of 6 months and is paying and#163;25-30 per hour dependant on experience.Interviews will take place week commencing 7th May.Please apply with an up to date version of your CV.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Mechanical  Stoke On Trent]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC86EC7B037D39126482579F5001BAB68</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Mechanical-Stoke-On-Trent_1638515.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Position: Design EngineerLocation: Stoke-on-TrentSalary: Flexible dependent on the candidateand#146;s experience. Competitive Key Skills: My client are a privately owned company currently market leader in the manufacture and supply of a large range of branded products in the fast growing utility, construction and industrial sectors. To support their ongoing business growth they are looking to recruit a Mechanical design Engineer; in this role you would be responsible to the Group Operations Manager working along side other key members of the management team and in close connection to the managing director.You need to be a hands on design engineer looking to get involve from concept right through to production and able to work with all areas of the business. Customer facing you will manage projects for and work with some of the biggest names in industry including Bombardier, Perkins and Many more.  This role will evolve and progress dependent on you skills and ambitions so itand#146;s key that you are looking for a diverse and varied role. To register your interest in this position please send in your CV ASAP to avoid disappointment to Kirsty McKinnon at Huxley Associatesand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Design Engineer  Mechanical]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob953EBB8CA1DA97E3482579F5001BAB7D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Principal-Design-Engineer-Mechanical_1638517.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[This growing business seeks a principal engineer to support the technical manager with existing workloads. You will be a senior member of the design team taking responsibility for existing and upcoming projects and working closely with key clients. You will work across a number of projects at any one time from existing product improvements to new product developments.   This will be a handand#146;s on role for an innovative engineer; with responsible for generation and delivery of concept and manufacturing designs. Responsibility will also be held for planning, controlling and delivering assignments to plan and within budget. You will need to work closely with customers and suppliers. Skills Needed: FEA AnalysisMS Office and#38; MS Project 3D CAD experience: Pro-E/ Solid Works Experience in a fast moving industry: i.e. consumer electronics, food, packaging, dispensing equipment etc beneficial  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Automotive Exeter]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob407B506C09665D8C482579F5001BAB95</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Automotive-Exeter_1638519.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Exeter area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? - Proven Mechanical Design Engineer- Catia V5- Automotive industry experienceFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Renewables Mechanical Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB1A47702A119A8B2482579F5001BABA8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Renewables-Mechanical-Engineer-Bristol_1638520.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focuses on designing and developing products for the renewable energy market.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Wind Turbine Experienceand#149;                     Offshore Structural ExperienceSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Site Quality Lead  8 Month contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB16E85631106B861482579F5001BABC0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Site-Quality-Lead-8-Month-contract_1638522.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client has an immediate Vacancy for a Project Site Quality Engineer to work on a 8 month contract based in the Midlands.The role will involve ensuring compliance with company policies and procedures throughout the project.The role will involves-Lead and support the site project team in Operational Quality Matters -Ensure upkeep of all Quality related documentation-Ensure escalation of any Quality related complaints or issues-Investigate and report all NCRand#146;s  and Quality Failures and Customer complaints and expedient  resolution of Quality issues-Prepare weekly performance summary and#38; monthly Quality performance reportsTraining and experience required-HNC in Quality Management-IEMA Certificate or equivalent-Minimum of 3 years experience within a Quality roleThe position will be based in the Nottinghamshire area and offered on an 8 month contract basis.  If you are interested in this role please forward a copy of your current CV.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Cheltenham]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4BD19AC9BBDC2AD8482579F5001BABD0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Cheltenham_1638523.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[NEW MECHANICAL DESIGN ROLE and#150; NPD and#150; GLOUCESTERSHIREA great opportunity has arisen to join a well established and well known manufacturing company who are about to undertake design for a brand new product range.My client is looking for a mechanical design engineer to join their team to work on the design and development of new products. This will be an interesting role where you will make a real contribution to this exciting new project and be involved from concept to completion.What they are looking for:-2/3 years mechanical design experiencePro E or UG CAD preferred (others considered)Experience in sheet metal or pressed metal idealIf you are looking for a new role in Mechanical Design please apply here for a swift response.This role not quite right? Please send me your CV or call me and I will be happy to discuss your ideal opportunity. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CAD Design Engineer  Pro Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9EFEF7FFF54E3B8A482579F5001BABE1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CAD-Design-Engineer-Pro-Engineer_1638525.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates and a world renowned engineering company in Gloucestershire are seeking a CAD Design Engineer.Your role will be to prepare and maintain project design layouts, production drawings considering methods or manufacture, tolerance and their effect on related parts or assemblies.You will prepare average complexity original mechanical layouts using the CAD system Pro Engineer and will prepare complex mechanical and average complexity electrical/electronic product/production drawings and other related documentation from layouts, sketches, or verbal instruction using the CAD system.Key Skills:- Understanding of mechanical and basic knowledge of electrical/ electronic product line - Pro Engineer- Electromechanical Design -  Manufacturing Technology -  Material Selection -  Mechanical System Design - Simulation and Modeling Please apply here for a swift response or please call Keira on 01179 388088 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Motors  up to £35k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0217BA677B015496482579F5001BABF0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Motors-up-to-and-amp-SHARP16335k_1638526.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am working with a successful manufacturing company based in Swindon who are part of a wider and#163;100m turnover group and are now looking for an Electromechanical Design Engineer. The company has a strong pipeline of work and opportunity for rapid expansion so therefore it will be great time to join and to enjoy career progression. In this role you will be working on the development of air movement products for general and bespoke requirements. Ideal Skills Sought: -Electro Mechanical Design Background -Sheet Metal Product Design -Product testing, approval and documentation -Reliability and failure mode analysis -CAD for electromechanical design My client would be interested in you if you have skills in:-- Motor Design- Rotating Machinery- Air Compression / Expansion- CastingsIt would be highly desirable if you have experience in design for air flow products.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob33B6CAC193DE5999482579F5001BAC01</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager_1638528.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Manager and Project Engineer Opportunities and#150; Berkshire Head office Huxley Associates are working with a leading civil engineering organisation who specialise within the water/ waste water industry. They are looking to increase turnover by 50% over the next 2 years following a recent acquisition. They understand that employees are vital to the progression of the company and as such are seen as key assets.Job Details:The key responsibilities are to run Civil Engineering projects for the key clients.The main attributes to be seen on a CV are the following:-Experienced within  Civil Engineering -Experienced with water/wastewater projects-Experience within a Project Engineering/Management role-Possess business acumen and commercial awareness -Ability to motivate and lead an engineering teamYou may have experience in the following roles: Project Manager, Project Leader, Project Engineer, programme manager, programme leaderSalary: Competitive and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Swindon  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob971DC477FCA03FC1482579F5001BAC0D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Swindon-Contract_1638529.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[POS Design Engineer and#150; Solidworks and#150; Swindon and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for 3 Month contract in Swindon.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. The role will require conceptual design all the way through to manufacture.Key Skills:and#149;Proficient with Inventorand#149;Proficient with Solidworksand#149;PhotoshopDay to Day:and#149;Designing products from laminate materials, sheet metals, fibreglass, wood and veneerIf you feel that you are a good fit for this role, then please send your CV in for immediate consideration.Rate: MarketDuration: 3 MonthsLocation: Swindon and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIORPRINCIPLE SOFTWARE ENGINEER CONTRACT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5F25EF945E5D31C3482579F5001BAC1D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/-SENIOR-PRINCIPLE-SOFTWARE-ENGINEER-CONTRACT_1638530.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My Client who are based in the Thames Valley area are looking for a senior/principle software engineer on a 3-6 month contract and to start next week! Essential Skills: - Coding c - c++ - Assembler/Assembley low lever programming - ARM - Multi Threading Desirer able Skills: - Cortex - Knowledge of OS structure If you are interested please call me today on 0118 956 5594  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Contract  Glasgow]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC34736C1092EEDBD482579F5001BAC2A</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Contract-Glasgow_1638531.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently looking for a Design Engineer to join a Subsea company in the Glasgow area; this is a brilliant opportunity to join a growing company.As the role of Design Engineer you will be expected to:and#149;Generate conceptual designsand#149;Write and check technical documentsand#149;Prepare reportsand#149;Verify designsand#149;Attend design reviews and check drawingsand#149;Prepare design layouts To be considered for this role you should have experience in the following:and#149;Degree in Mechanical Engineering or similar disciplineand#149;Understanding of test proceduresand#149;Soildworks, unigraphics (or similar package), MathCAD, FEA, Ansysand#149;Calculationsand#149;Working to industry standardsand#149;Technical documentsand#149;5 years + experience in roleand#149;Subsea equipmentand#149;Landing stringsand#149;Heavy engineering ( if no subsea exp) I am looking for someone who is responsible and not afraid to make their voice heard when working as part of a team. It is desirable if you have Oil and Gas experience however if you have transferable skills and the strong attributes you may be considered for this role. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solidworks Design Engineer  £2530hour]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFBC60F2ACF5028F4482579F5001BAC3B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solidworks-Design-Engineer-and-amp-SHARP16325-30-hour_1638532.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client based in the Midlands has an immediate requirement for a Design Engineer on a contract basis.Ideally the candidate will have previous experience of plastic injection moulded parts design. The majority of the work will be on injection moulded valve design with little work on sheet metal and machined parts. The work with plastics is central to the project and forms 90% of the work and 99% of the project risk.The contract will run for a minimum of 4 months and is paying and#163;25-30 per hour dependant on experience.My client is looking for a candidate who has a sound knowledge of Solidworks. Interviews will take place next week.Must have good communication and presentation skills as the position will be required to liaise with the client and suppliers. Ideally educated to a degree level or the equivalent in experience.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manufacturing Process Engineer  Medical  £55,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob05CC3EE90D979A98482579F5001BAC51</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Manufacturing-Process-Engineer-Medical-and-amp-SHARP16355000_1638533.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is a manufacturer of products for the diagnosis of infectious diseases.The JobMy client is looking for a Manufacturing Process Engineer to be the technical lead for the development of disposable cartridge manufacture . The primary responsibility will be to act as technical interface and project leader for our cartridge manufacture working on the manufacturing development project. Person Specification:The ideal candidate will bring with them/be:Degree or equivalent in mechanical engineering, electrical engineering or physicsAt least 5 years hands-on within a medical manufacturing environmentIVD/medical device semi-automatic/fully automatic manufacturingOperating to Quality Management and#38; Regulatory frameworks relevant to IVD/medical devicesProcess validation General Skills:Leading projectsOperating within multi-company matrixTechnical and progress data presentationStrong verbal and#38; written communicationComfortable working with Senior ManagementWilling to ask questions and challenge proposalsSalary: to and#163;55k Plus Package To apply, please attach your CV and/or call Akeela Tuffail on 0118 956 5545 for an immediate response.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Purchasing Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBFDA9D8F3DD062E7482579F5001BAC60</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Purchasing-Manager_1638534.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Southampton is currently looking to employ a Purchasing Manager. The successful candidate will have:Manufacturing background and#150; need to understand engineering processes, manufacturing planning and to maintain credibility within the businessStrong supplier work and#150; selecting new suppliers, lead supplier agreements and manage thesePurchasing knowledge and#150; purchasing for NPI and#38; current manufacturing requirements, supplier management, contract management and costingExperience with ERP/MRPCommunication skills: dealing with customers, suppliers and negotiation CIPS is desirable, but not essentialThe role will involve, but duties are not limited to:Strategic management of procurementDevelop the purchasing strategy which will create cost downWorking very closely with suppliers: sourcing, selection and#38; developmentDeveloping the Strategic Purchasing department to support additional membersDevelop purchasing team The successful candidate will benefit from a salary of up to and#163;45,000 and a good package If you are interested in applying for this position please attach your CV, including salary expectations, and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3389646740075F48482579F5001BAC6D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager_1638535.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Southampton is currently looking to employ a Procurement Manager. The successful candidate will have:Manufacturing background and#150; need to understand engineering processes, manufacturing planning and to maintain credibility within the businessStrong supplier work and#150; selecting new suppliers, lead supplier agreements and manage thesePurchasing knowledge and#150; purchasing for NPI and#38; current manufacturing requirements, supplier management, contract management and costingExperience with ERP/MRPCommunication skills: dealing with customers, suppliers and negotiation The role will involve, but duties are not limited to:Strategic management of procurementDevelop the purchasing strategy which will create cost downWorking very closely with suppliers: sourcing, selection and#38; developmentDeveloping the Strategic Purchasing department to support additional membersDevelop purchasing team The successful candidate will benefit from a salary of up to and#163;45,000 and a good package If you are interested in applying for this position please attach your CV, including salary expectations, and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  PROE  Plymouth]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1A57735D10780F2A482579F5001BAC82</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-PROE-Plymouth_1638536.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Apologies is this requirement does not match your skill setMechanical Design Engineer and#150; Contract and#150; Plymouth and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range.Essentials:and#149;Pro Engineer as main CAD Package (Wildfire 4 Desirable)and#149;Injection Moulding experienceand#149;Plastics Experienceand#149;FMEA Experienceand#149;Experience of Design Reviewand#149;Excellent communication skills with the ability to interact at all levels and is a pro-active team member. and#149;Communication skills include written reports, presentations and cross-functional team activity. Responsibilities:and#149;Finishing off the 3D Designsand#149;Providing the Mechanical Analysisand#149;Providing the Design ReviewThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Rate: MarketLocation: PlymouthDuration: 3 Monthsand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[INTERIM SENIOR BUYER  SOUTHAMPTON   6 MONTHS]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob89EB5E609AEF5310482579F5001BACA1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/INTERIM-SENIOR-BUYER-SOUTHAMPTON-6-MONTHS_1638538.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client, an industry leader in composite components have a versatile and varied opportunity for a Senior Buyer to join their busy Purchasing department on a long term interim basis. Key responsabilities:- Managing and controlling all the companys external suppliers- Ensure parts and materials are bought at the most competitive price and delivered on time for production -Identify new suppliers, agree terms and negotiate supply agreements where appropriate -Forge close working relationships with associated departments -Continually improve purchasing methods and drive down external spend As well as this you must have good general IT skills as well as the ability to develop relationships with people at all levels so superior communication skills are paramount. The ability to remain organised, to work effectively under pressure and to strict deadlines are also key attributes required to be successful in this position.  Please send me your up to date CV andif you are sucessful I will call you back to discuss the role in further detail. Please note we will only contact those candidates that we feel are suitable for the positions we have currently available. If you dont hear from us within 5 working days, please accept our apologies but we are unable to help you on this occasion.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Senior Buyer  South West  URGENT!!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6651FC3BAF1022E6482579F5001BACB4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Senior-Buyer-South-West-URGENT_1638540.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is looking to employ an Interim Senior Buyer, to be part of their purchasing department. The role is an exciting opportunity to join a successful business with solid and exciting growth plans.The successful candidate will: Purchasing raw materials to support projectsLiaise with site managers and purchasing team to ensure smooth flow of materialsNegotiate and manage large value and long-term contracts Help develop purchasing team, by supporting junior team membersBe involved with developing company and supporting growth plansYou will be able to demonstrate the below: Procurement: Strong, proven purchasing experience. Communication: need to be able to liaise between site managers and teamContract Management Industry understanding: experience within rail, highways or construction You must hold a full driving licence and be able to travel  PLease send me your up to date CV and if you are sucessful I will give you a call back to discuss the role further.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Plymouth  Pro E]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob61C20A9FC1459285482579F5001BACD5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Plymouth-Pro-E_1638542.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Mechanical Design Engineer and#150; Contract and#150; Plymouth and#150; 3 MonthsHuxley associates are currently looking for a Mechanical Design Engineer on 3 month contract.The role has come about to assist the design team with a number of new products to their existing range. Essentials:and#149;Pro Engineer as main CAD Package (Wildfire 4 Desirable)and#149;Injection Moulding experienceand#149;Plastics Experienceand#149;FMEA Experienceand#149;Experience of Design Reviewand#149;Excellent communication skills with the ability to interact at all levels and is a pro-active team member. and#149;Communication skills include written reports, presentations and cross-functional team activity.Responsibilities:and#149;Finishing off the 3D Designsand#149;Providing the Mechanical Analysisand#149;Providing the Design ReviewThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role, this role is due to start at the early part of next week.Rate: MarketLocation: PlymouthDuration: 3 Monthsand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Buyer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEC07F32D8DEB03AC482579F5001BACE1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Buyer_1638543.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is looking to employ a Senior Buyer, to be part of their purchasing department. The role is an exciting opportunity to join a successful business with solid and exciting growth plans.The successful candidate will: Purchasing raw materials to support projectsLiaise with site managers and purchasing team to ensure smooth flow of materialsNegotiate and manage large value and long-term contracts Help develop purchasing team, by supporting junior team membersBe involved with developing company and supporting growth plansYou will be able to demonstrate the below: Procurement: Strong, proven purchasing experience. Communication: need to be able to liaise between site managers and teamContract Management Industry understanding: experience within rail, highways or construction You must hold a full driving licence and be able to travel The successful candidate will benefit from a competitive salary of up to and#163;50,000 plus a good package  If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Manager London  UK wide 40k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBC24366DB810B420482579F5001BACEE</referencenumber>
<City><![CDATA[UK WIDE]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Manager-London-UK-wide-40k_1638544.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Award wining Huxley Associates are proud to be working exclusively with one of UKand#146;s leading UPS manufacturers. Part of an international group they are a specialist in the design and manufacture of high power UPS systems. This company have established themselves as a market leader not only throughout the UK but on a global front. Due to internal promotion and a restructure in their sales team they now have a vacancy in their sales team. Working from home and reporting to the senior management team you will be selling to contractors and consultants predominantly in the London region (but also UK wide) focusing on the data centre and financial markets. Key responsibilities will include: and#149; Search and prospect for new clients and develop existing client base and#149; Travel to visit potential clients and provide technical site/installation/product based support and#149; Preparing client quotations and proposals and#149; Negotiating tender and contract terms  Minimum requirements for the role are: and#149; Proven track record of technical sales and#150; within UPS, generators or switchgear and#149; An electrical or building services engineer qualified to degree level and#149; Ability to negotiate commercial contracts. and#149; Proven relationship building skills In return you can expect a salary somewhere in the region of and#163;30-40k with car, pension and healthcare on top. So if you are interested in taking your career that one step further and want to work for a dynamic and forward thinking organisation, please apply nowand#133; and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  CONTRACT  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBBF0452379F38E5B482579F5001BACFF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-CONTRACT-URGENT_1638545.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[POS Design Engineer and#150; Solidworks and#150; Swindon and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for 3 Month contract in Swindon.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. The role will require conceptual design all the way through to manufacture.Key Skills:and#149;Proficient with Inventorand#149;Proficient with Solidworksand#149;PhotoshopDay to Day:and#149;Designing products from laminate materials, sheet metals, fibreglass, wood and veneerIf you feel that you are a good fit for this role, then please send your CV in for immediate consideration.Rate: MarketDuration: 3 MonthsLocation: Swindon and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[POS Design Engineer  Swindon  3 Month Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob824BA2E63A047B5B482579F5001BAD0C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/POS-Design-Engineer-Swindon-3-Month-Contract_1638546.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[POS Design Engineer and#150; Solidworks and#150; Swindon and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for 3 Month contract in Swindon.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. The role will require conceptual design all the way through to manufacture.Key Skills:and#149;Proficient with Inventorand#149;Proficient with Solidworksand#149;PhotoshopDay to Day:and#149;Designing products from laminate materials, sheet metals, fibreglass, wood and veneerIf you feel that you are a good fit for this role, then please send your CV in for immediate consideration.Rate: MarketDuration: 3 MonthsLocation: Swindon and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Plant Manager  Northampton  Manufacturing]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8C562B3ED767F4FE482579F5001BAD21</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Plant-Manager-and-amp-SHARP150-Northampton-and-amp-SHARP150-Manufacturing_1638547.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is proud to be working exclusively with a leading manufacturer which design and manufacture a variety of cutting edge products within the plastics industry.An opportunity has arisen for a new Site Manager to join their Northampton site which presents an excellent opportunity. This is an excellent chance to head up a site currently with and#163;8 million turnover and 60 employees who are currently very successful. What is really positive about this company though is that there is a huge amount of opportunity on this plant to take it to the next level.Interested? I am looking for some of the strongest Plant Managers / Operations Managers within the engineering or manufacturing industry. The most important aspect of this role is that you are an excellent man manager who is genuinely strong at leading and getting the best out of a team. Any experience in the plastics industry and/ or lean experience would be desirable but is not essential.  On offer for the role is a starting salary of and#163;45,000- and#163;50,000 which is flexible dependant on the successful candidates skills and experience. There is also a generous benefits package which includes a company car or car allowance (and#163;7500), bonus, contributory pension and healthcare.Interested? This is an urgent role with shortlisting occurring now so please apply online to Brooke Whitehead at Huxley Associates ASAP in order to avoid disappointment. NB. This role may be suitable for, but is not limited to, the following job titles: Site Manager, Plant Manager, Operations Manager, Operations Director, Manufacturing Manager, Production Manager.This role is commutable from: Northampton, Northamptonshire, Rugby, Corby, Coventry, Milton Keynes, Peterborough, Wellingborough, East Midlands, Midlands.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Renewables Mechanical Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob79AA40A95A58A05A482579F5001BAD2D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Renewables-Mechanical-Engineer-Bristol_1638548.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focuses on designing and developing products for the renewable energy market.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Wind Turbine Experienceand#149;                     Offshore Structural ExperienceSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Renewables engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob59C5A6BB75A0D1F6482579F5001BAD3B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Renewables-engineer-Bristol_1638549.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focuses on designing and developing products for the renewable energy market.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Wind Turbine Experienceand#149;                     Offshore Structural ExperienceSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Renewables Mechanical Engineer Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5EDB1CEEB02C3973482579F5001BAD4C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Renewables-Mechanical-Engineer-Bristol_1638550.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an exciting new opportunity for a senior mechanical design engineer to join a well established business based in Bristol.My client focuses on designing and developing products for the renewable energy market.This is fantastic opportunity for an ambitious individual to work as part of a well established business and contribute to itand#146;s success and growth through the development of new products.What they are looking for? and#149;                     Wind Turbine Experienceand#149;                     Offshore Structural ExperienceSalary is on offer upto and#163;40,000 + benefits.Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Director  (Hampshire) £85k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob227A4CA8F42A60F8482579F5001BAD5A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electrical-Director-Hampshire-and-amp-SHARP16385k_1638551.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[The Company: Our client is a leading Renewable Energy company based in the Hampshire and are looking to recruit for a Head of Electrical Engineering. The Job The Engineering Director will have management and technical responsibility for all aspects of electrical and communications engineering. The key objective of this role will be to further develop my clients expertise and project delivery of the electrical engineering during all phases of the Project development cycle. Experience Required: Studied to degree level or higher within Electrical Engineering/Systems Experience within the wind, renewables or solar industry Experienced within the Electrical Industry Knowledge and experience of Grid code/ Grid Integration Experience in managing budgets Design , procurement and construction of electrical balance of plant Electrical systems design, integration and analysis Construction Health and Safety legislation and Rules applicable to electrical engineering Salary: and#163;85,000 plus Life insurance/Medical/ 30 days holiday/10% pension contribution and#38;15 % bonus To apply, please attach your CV and/or call Akeela Tuffail on 0118 956 5545 for an immediate response. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Inspector Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCD96F869BC95DC2E482579F5001BAD71</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Inspector-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638552.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Inspectorand#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob106D8D9C477DC5FD482579F5001BAD7D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager_1638553.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A small but successful project business based in Sussex is currently looking to recruit a Commercial Manager. This is a new position within the company to ensure continued development of the company and developing strong purchasing techniques The successful candidate will have:Experience working on projects, ensuring they come in under costExperience liaising between Project Managers and other key members of the teamStrong vendor management and contract negotiation experienceBe used to working with high value contractsThe successful applicant will be responsible for:Cost control across all projectsMonthly applications for all projects (where applicable)Procurement of all project purchasesDiscount incentive schemes with major suppliersMaximising invoice potential per monthAgreement with Contractors where applications disputed The successful candidate will benefit from a salary of up to and#163;35,000If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer RefridgerationHeating]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF28ACF42524CAEBA482579F5001BAD8D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Refridgeration-Heating_1638554.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? -Experience of working within heating/refridgeration industry-Mechanical experience/backgroundFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HeatingRefridgeration Experience Bristol £45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D59B66632B54043482579F5001BAD9A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Heating-Refridgeration-Experience-Bristol-and-amp-SHARP16345000_1638555.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? -Experience of working within heating/refridgeration industry-Mechanical experience/backgroundFull company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Commercial Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7309CE64081FCEE4482579F5001BADA9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Commercial-Manager_1638556.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A small but successful project business based in Sussex is currently looking to recruit a Commercial Manager. This is a new position within the company to ensure continued development of the company and developing strong purchasing techniques The successful candidate will have:Experience working on projects, ensuring they come in under costExperience liaising between Project Managers and other key members of the teamStrong vendor management and contract negotiation experienceBe used to working with high value contractsThe successful applicant will be responsible for:Cost control across all projectsMonthly applications for all projects (where applicable)Procurement of all project purchasesDiscount incentive schemes with major suppliersMaximising invoice potential per monthAgreement with Contractors where applications disputed The successful candidate will benefit from a salary of up to and#163;35,000If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBD491AC7F7D75DAE482579F5001BADB5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager_1638557.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Manager and/or Project Engineer and#150; Berkshire - circa and#163;35,000 -and#163;45,000Huxley Associates are working with a large multinational organisation in Berkshire to recruit for Project Manager / Project Engineering positions. Our client operates within the food and beverage industry providing to a global region. They understand that employees are vital to the progression of the company and as such are seen as key assets.Job Details:The key responsibilities are manager engineer lifecycles from initial concept across supporting manufacture to commissioning.The main attributes to be seen on a CV are the following:-Background within the food industry-Experience in a project engineering or project management role and#150; at least 3 years-Degree qualified or equivalent within mechanical or chemicalYou may have experience in the following roles: Project Management, Project Leader, Delivery Project Manager, Project Engineer Salary: circa and#163;35,000 -and#163;45,000 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurenemt Manager  Thames Valley  9 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEF4DCD97DC5BB3BE482579F5001BADC4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurenemt-Manager-Thames-Valley-9-Months_1638559.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading company in the Automotive sector based in the Thames Valley area to recruit an Interim Procurement Manager with strong Supply Chain skills.  We are looking for someone who has a proven career history as a Supply Chain Manager / Procurement Manager and can bring strong strategic knowledge to reduce costs and manage inventory levels to ensure they can deliver to clients needs.This will be a great role for an experienced candidate who wants to develop and implement procurement strategy, lead strategic sourcing, be involved in pricing and contract negotiation, manage inventory and stock levels to reduce cost, manage and grow supplier relationships and rationalise the supplier base and product lines.    To be considered we want to see you have the skills and experience to lead their Procurement team and bring about cost savings through the introduction of new Supply Chain and Procurement strategies.  It is very likely you will have a proven track record in the Automotive/Composites industry.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interim Supply Chain Planner  612 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDD32230E6E5ACAFE482579F5001BADD1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interim-Supply-Chain-Planner-6-12-Months_1638560.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturing company based in Guildford is currently looking to hire an Interim Supply Chain Planner. This is an excellent opportunity to join a hugely successful, global company with impressive career progression opportunities. The successful candidate will have:- Significant experience in a similar Supply Chain role in manufacturing- Experience working with and developing Kanban and OTD- Detailed MRP experience - Very strong inventory management experience - Experience managing teamsKey responsabilities include:- Responsible for all material movement and stock levels- Responsible for Inventory Management- Help improve OTD- Responsible for line management of several team leaders within this function- Create and control the master schedule for all manufactured products- Coach and support teamand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Export Sales Manager  Utilities  Meters]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0231C713CA5ED69D482579F5001BADE2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Export-Sales-Manager-Utilities-Meters_1638561.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Export Sales Manager. Working with a leading Meter manufacturer based in the UK.You will have a proven background of high value export sales selling technical products such as data loggers or meters.Key Skills:International export sales experience, ideally within a utilities related market* Commercial competence with experience of negotiating at a high level* Comprehensive commercial skills.* A sufficient technical background  - Metering and#38; data loggersA qualification in  Engineering would be beneficial, as well as additional languages and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Planner & Allocator (Fashion), regio Maastricht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDBABFE56C2A7AC22482579F5001BAE12</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Planner-and-amp-SHARP38-Allocator-Fashion-regio-Maastricht_1638566.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Onze opdrachtgeverVoor een toonaangevend bedrijf in de fashion-branche ben ik op zoek naar een planner and#38; allocator in de regio Maastricht.De functie Als Planner and#38; Allocator ben je verantwoordelijk voor het realiseren van een optimale omzet en marge door het sturen van de goederenstroom van all segmenten in de winkels, je rapporteert direct aan de Country Manager.Taken and#38; verwantwoordelijkheden- opstellen van inkoopbudgetten and#38; afprijsbudgetten voo de winkels- bewaken and#38; analyseren van de KPIand#146;s and#38; op basis hiervan verbeteringen voorstellen- forecasts mbt omzet, voorraad, afprijzingen maken- optimale goederenverdelingen- samenwerking met de merchandisers, marketing, stockaccounting en planning and#38; allocation- doorvoeren van afprijzingen in de systemen Functie-eisenVoor deze functie is minimaal een HBO opleiding vereist, aangevuld met min. 3 jaar werkervaring binnen de fashion/retail branche. Bekend met Excel, futura en SAP. Je beheerst de Nederlandse, Engelse en Duitse taal goed en je hebt een sterk cijfermatig inzicht. Je bent analytisch en hebt oog voor de klant. Je bent pro-actief en flexibel. Geinteresseerd? Reageer direct via onderstaande link met een up to date cv of bel tav Sanne Wissels op 020 522 1333 voor meer informatie. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solidworks  Design Engineer  Cheltenham]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob62B5CBCF32BC2540482579F5001BAE21</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solidworks-Design-Engineer-Cheltenham_1638567.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Asscociates are currently looking for a number of Design Draughtsman in the Cheltenham area.Our client, a market leading special purpose machinery manufacturing company are looking for Engineers on a rolling contracts. The Engineers will be working across a number of industries throughout the world with a variety of clients and products.  The roles will involve working along side all other departments within the company supporting the project manager as the senior design engineers. Working with solidworks and later Inventor, depending on your experience you could be updating, modifying detailing developing and creating conceptual designs of electro-mechanical PLC controlled pieces of equipment. You will co-ordinate and liaise with manufacturing and sit in on design review meetings to discuss NPI. The work will be a mixture of new orders that have come in and will be manufactured next year and also work that is going to be integrated into already installed systems on clients sites.  You will also be responsible for being the deputy within the team, supervising and even managing design draughtsman and workload.The technical aspects of being able to understand the kit and the systems are essential.  You will be given full induction and training on the systems thouh you must have some technical electro-mechanical systems manufacturing background.  Someone with good hands on experience from a solid production/manufacturing background with the ability to create and work with large bill of materials as well. A high level of enthusiasm, professionalism and taking pride in the work you do are also required. The successful candidate: and#149; Solidworks at least 3 years experience in Industryand#149; HNC Qualified and#149; Electro-mechanical Systems Product backgroundRate: MarketDuration: 6 MonthsLocation: Cheltenhamand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  CONTRACT  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7F99836B7093D1FF482579F5001BAE31</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-CONTRACT-URGENT_1638568.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design Engineer and#150; Solidworks and#150; Cornwall and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for a 6 Month contract in Cornwall.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. Also they will be produce detailed design drawings for fabrications and machined parts.Day to Day Roles:Production of conceptual design schemes in 2D and 3D.and#149; Production of detailed design schemes in 2D and 3D.and#149; Production of detailed engineering hand calculations and FE analysis.and#149; Production and submission of 3rd party design verification reports.and#149; Production of detailed 2D engineering drawings for manufacture.and#149; Participate in regular formal design reviews as required.and#149; Creation and adherence to project schedules as required Essential Skills: Qualified to Degree/HND level.and#149; Minimum of 5 years experience in heavy engineering, preferably drilling related.and#149; Proficient in the use of SolidWorks 3D design package.and#149; Proficient in the use of AutoCAD 2D for conceptual design set outs.and#149; Preferably familiar and proficient with Staad Pro.and#149; Proficient in the production of hand calculations.and#149; Familiar in the use of engineering analysis software, preferably SolidWorks Simulation.and#149; Computer literate in Microsoft office suite.and#149; Display good time keeping.and#149; Display a willingness to integrate and work within a team.Location: CornwallDuration: 6 MonthsRate: Marketand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanhical Design Engineer  Cornwall  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA0BD8C2320B85D9D482579F5001BAE3F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanhical-Design-Engineer-Cornwall-6-Months_1638569.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design Engineer and#150; Solidworks and#150; Cornwall and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for a 6 Month contract in Cornwall.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. Also they will be produce detailed design drawings for fabrications and machined parts. Day to Day Roles:Production of conceptual design schemes in 2D and 3D.and#149; Production of detailed design schemes in 2D and 3D.and#149; Production of detailed engineering hand calculations and FE analysis.and#149; Production and submission of 3rd party design verification reports.and#149; Production of detailed 2D engineering drawings for manufacture.and#149; Participate in regular formal design reviews as required.and#149; Creation and adherence to project schedules as requiredEssential Skills: Qualified to Degree/HND level.and#149; Minimum of 5 years experience in heavy engineering, preferably drilling related.and#149; Proficient in the use of SolidWorks 3D design package.and#149; Proficient in the use of AutoCAD 2D for conceptual design set outs.and#149; Preferably familiar and proficient with Staad Pro.and#149; Proficient in the production of hand calculations.and#149; Familiar in the use of engineering analysis software, preferably SolidWorks Simulation.and#149; Computer literate in Microsoft office suite.and#149; Display good time keeping.and#149; Display a willingness to integrate and work within a team.Location: CornwallDuration: 6 MonthsRate: Marketand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  South West  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD416F5D73F71ED9C482579F5001BAE4E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-South-West-6-Months_1638570.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design Engineer and#150; Solidworks and#150; Cornwall and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for a 6 Month contract in Cornwall.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. Also they will be produce detailed design drawings for fabrications and machined parts. Day to Day Roles:Production of conceptual design schemes in 2D and 3D.and#149; Production of detailed design schemes in 2D and 3D.and#149; Production of detailed engineering hand calculations and FE analysis.and#149; Production and submission of 3rd party design verification reports.and#149; Production of detailed 2D engineering drawings for manufacture.and#149; Participate in regular formal design reviews as required.and#149; Creation and adherence to project schedules as requiredEssential Skills: Qualified to Degree/HND level.and#149; Minimum of 5 years experience in heavy engineering, preferably drilling related.and#149; Proficient in the use of SolidWorks 3D design package.and#149; Proficient in the use of AutoCAD 2D for conceptual design set outs.and#149; Preferably familiar and proficient with Staad Pro.and#149; Proficient in the production of hand calculations.and#149; Familiar in the use of engineering analysis software, preferably SolidWorks Simulation.and#149; Computer literate in Microsoft office suite.and#149; Display good time keeping.and#149; Display a willingness to integrate and work within a team.Location: CornwallDuration: 6 MonthsRate: Marketand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PLC Controls Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3158D7FDF1F54C0C482579F5001BAE68</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/PLC-Controls-Engineer_1638571.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[PLC Controls Engineer - 6 month contract - DevonHuxley Associates has an immediate requirement for a PLC Controls Engineer to work on an initial 6 month contract for a client located in Devon.Controls Engineer with PLC experience to work on a safety circuit upgrade project.This project will run for a minimum of 6 months.The Controls Engineer will need to:-supervise the upgrade to Cat 3 PL D of approximately 50 machines.-plan the upgrade work in conjunction with the production team. -supervise modifications.-checking work before re-commissioning equipment.A certain amount of safety circuit design skills will be required.We need someone who can fault find and programme PLCs including Siemens and Mitsubishi.If you are interested in a new contract opportunity then please apply.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob12B2541B9D874369482579F5001BAE77</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electrical-Design-Engineer_1638572.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Electrical Design Engineer - 6 Month Contract - BristolHuxley Associates has an immediate requirement for an Electrical Design Engineer on a contract basis. As an Electrical Design Engineer you will work as part of a multi-disciplined team developing PLC-based control systems for exhaust gas management products.Key activities will include:-Development of control system specifications.-Specification of components.-Circuit protection design.-Preparation of electrical and control schematics.-Electrical panel design.-Preparation of bills of materials.-Preparation of design brief for electrical drafting.-Supervision and checking of drafting.-Organisation and supervision of third-party electrical safety assessments.-Organisation and supervision of prototype product fabrication.-Support of product in factory test and on customer sites.If you are interested in a new contract opportunity then please apply.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Thermodynamics  Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob31174A56BCE1230A482579F5001BAE84</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Thermodynamics-Bristol_1638573.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? -Thermodynamics- Catia V5Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Engineer Thermodynamics experience]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4E1C5EFBCB7A0B9E482579F5001BAE93</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Engineer-Thermodynamics-experience_1638574.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are currently working with an exciting SME based in the Bristol area who are now looking to recruit a Mechanical Design Engineer. You will join a small design team where you will be fully involved in the product development cycle and will make a real contribution to the team. Great career development opportunities available. What they are looking for? -Thermodynamics- Catia V5Full company details available upon request - I look forward to hearing from you.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC0C7232FB65B90C7482579F5001BAEA1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-Manager_1638577.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client is looking to employ a Contract Manager, to be part of their purchasing department. The role is an exciting opportunity to join a nationwide and highly successful business. The successful candidate will: Identify material requirements from involvement with projectsPlan purchasing strategy, identify suppliers, engage and implement procurement strategyProject specific supplier evaluation and selectionRepresent supplier agreements in SAP to enable accurate purchasingPrepare detailed bid documents for supply chain and project purchasingManage procurement process on a commission, throughout and to end of projectUse data to report on project procurement cost savings against allowance You will be able to demonstrate the below: Procurement: Strong, proven purchasing experience. Communication: being able to influence suppliers and#38; clients. Understanding business needs and goals to develop strategy and gain buy-in. Negotiation: Track record in ethical, firm and fair negotiationsCost SavingsIndustry understanding: experience within rail, highways or construction You must hold a full driving licence and be able to travel The successful candidate will benefit from a competitive salary of up to and#163;48,000 + Car + BonusesIf you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design EngineerProfessional Development Supported]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9DFA39943FFA554C482579F5001BAEB0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Professional-Development-Supported_1638578.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you an innovative Mechanical Design Engineer? Do you want to work for one of the UKand#146;s fastest growing Oil and#38; Gas manufacturers? Huxley Associates are working with a leading supplier to the Subsea industry in their search for a Mechanical Design Engineer. Based in Manchester, the company have increased their turnover by over 200% in five years and can offer excellent opportunity for Design Engineers with a strong mechanical understanding and a passion for engineering. Ideally Degree educated, the successful applicant will have a good knowledge of materials application and machining processes. There are no fixed criteria regarding industry or product background although experience of designing complex and precision parts would be beneficial. To give you some background, every Design Engineer I have placed here since 2006 has stayed with them because: 1) they listen to staff and implement their ideas2) the tedious parts of Design have been eliminated (e.g. BOMs, schematics) 3) they support staff in obtaining Chartered Status 4) they have revolutionised manufacturing in their field 5) they allow staff to share in the success which could lead to significant reward6) they invest heavily in NPD, new machinery, and staying ahead of the game 7) they have bypassed the recession and are one of the fastest growing companies in the field It sounds too good to be true but its not! To back this up, in the event of you receiving a job offer here, I would ask you to speak directly to a Design Engineer already working there to verify.For consideration, please send your CV to Liz Neidhardt at Huxley Associates. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5669588033BE2678482579F5001BAEBF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638579.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Engineer and#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance, Automotive Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob91966ECC57E29B59482579F5001BAED8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Automotive-and-amp-SHARP150Somerset_1638580.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Assurance and#150; Automotiveand#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Solid Works]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA10C17651877072F482579F5001BAEEA</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[Midlands East]]></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Solid-Works_1638582.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client has won a major role in a contract with the US Army for the design and build of a long endurance air vehicle surveillance solution. Based on lighter than air technology, this development programme opens a considerable market opportunity, with the demand for cost effective and highly flexible air vehicle solutions in both surveillance and heavy lift.As a result my client is looking to expand its work force and have an immediate requirement for a Design Engineer on a 3 month contract basis.Ideally you will be proficient in using Solid Works.My client will also obtain security clearance for the successful applicant.This is an immediate requirement.and#163;20-30 per hour with unlimited hours on offer. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Unigraphics Design Engineer  6 month contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob96C856DC0ABB4865482579F5001BAEF6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Unigraphics-Design-Engineer-and-amp-SHARP150-6-month-contract_1638583.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A key client based in the Midlands has an immediate requirement for a Design Engineer.Ideally the candidate will have previous experience of yellow goods within a heavy engineering capacity.The contract will run for duration of 6 months and is paying and#163;25-27 per hour dependant on experience.You will be required to undertake the administrative aspects of drawing release and product structuring. Candidate should have previous experience of mechanical design of components and systems.My client is looking for a candidate who has a sound knowledge of Unigraphics NX4 to 7.5. Interviews will take place next week.Must have good communication and presentation skills as the position will be required to liaise with the client and suppliers. Ideally educated to a degree level or the equivalent in experience.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Autodesk Inventor Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC7A6C7E0EEF3963E482579F5001BAF07</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Autodesk-Inventor-Contract_1638584.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a Design Engineer on 3 month contract.This role has arisen due to an increase in project that the company have taken on. The candidate will primarily be designing components using Autodesk Inventor.Requirements:and#149;Hard Work Ethicand#149;Innovative Thinkingand#149;Excellent communication skillsand#149;Working to pre defined set targetsResponsibilities:and#149;Working as part of the 3D Design Teamand#149;Working with Autodesk Inventorand#149;Liaising with design managerand#149;Liaising with suppliers and clientsand#149;Some 2D AutoCAD DrawingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role if you are interested.Rate: MarketLocation: SouthWestDuration: 3 Months and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[AutoDesk contract design engineerer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7E6710CDA02D29BF482579F5001BAF15</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/AutoDesk-contract-design-engineerer_1638585.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a Design Engineer on 3 month contract.This role has arisen due to an increase in project that the company have taken on. The right candidate will be making bespoke changes to an already existing product range to suit their customersand#146; requirements.Requirements:and#149;Hard Work Ethicand#149;Innovative Thinkingand#149;Excellent communication skillsand#149;Working to pre defined set targetsResponsibilities:and#149;Working as part of the 3D Design Teamand#149;Working with Autodesk Inventorand#149;Liaising with design managerand#149;Liaising with suppliers and clientsand#149;Some 2D AutoCAD DrawingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role if you are interested.Rate: MarketLocation: BristolDuration: 3 Months and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ISO14001,TS16949  Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob428E743911A18176482579F5001BAF22</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ISO14001TS16949-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638586.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Assurance and#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob046BEFF4DA6CBBDD482579F5001BAF2F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638587.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Assurance and#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Permanent Somerset]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob54C43F2BB86FEED4482579F5001BAF3F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-and-amp-SHARP150-Permanent-and-amp-SHARP150Somerset_1638588.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Quality Engineer and#150; Permanent and#150;SomersetHuxley associates are currently looking for a Quality Engineer to be a permanent addition to their team.My client produces specialised products for the automotive industry and is one of the most established companies within the business.  The main purpose of the role is to liaise with customers in all aspects of product quality and be able to report back accordingly.Essentials:-Understanding of Quality Systems- TS16949-Mechanical Understanding-Knowledge of ISO14001This is an urgent role for Huxley Associates so if you are interested please apply by sending across an up to date CV or call Varinder on 0117 9388088.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[AutoDesk Inventor  Contract  South West]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFB21E6031BA3724A482579F5001BAF54</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/AutoDesk-Inventor-Contract-South-West_1638589.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a Design Engineer on 3 month contract.This role has arisen due to an increase in project that the company have taken on. The right candidate will be making bespoke changes to an already existing product range to suit their customersand#146; requirements.Essentials:and#149;Experience with Autodesk Inventorand#149;3D Modelling Experienceand#149;Excellent communication skillsand#149;Working to pre defined set targetsResponsibilities:and#149;Working as part of the 3D Design Teamand#149;Component modellingand#149;Liaising with design managerand#149;Liaising with suppliers and clientsand#149;Some 2D Autocad DrawingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role if you are interested.Rate: MarketLocation: South WestDuration: 3 Months and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Contract  Bristol]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob70A4ADDE793994A9482579F5001BAF64</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Contract-Bristol_1638590.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley associates are currently looking for a Design Engineer on 3 month contract.This role has arisen due to an increase in project that the company have taken on. The right candidate will be making bespoke changes to an already existing product range to suit their customersand#146; requirements.Essentials:and#149;Experience with Autodesk Inventorand#149;3D Modelling Experienceand#149;Excellent communication skillsand#149;Working to pre defined set targetsResponsibilities:and#149;Working as part of the 3D Design Teamand#149;Component modellingand#149;Liaising with design managerand#149;Liaising with suppliers and clientsand#149;Some 2D Autocad DrawingThis is an urgent role for Huxley Associates and the client can only consider immediately available candidates. Send in your CV for immediate consideration for this role if you are interested.Rate: MarketLocation: BristolDuration: 3 Months and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Required Lancashire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobED3F710B82C8ECED482579F5001BAFA6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Required-Lancashire_1638593.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My exclusive client, a market-leading design and manufacture company within the Oil and#38; Gas industry, are looking to recruit a Mechanical Design Engineer on an initial 6 month contract having landed a major project which will guarantee work at the company for the foreseeable future.An immediate start is available for the right candidate and I am assured that the rate on offer is EXTREMELY COMPETITIVE.The ideal candidate should possess as many of the following as possible:- Inventor 3D CAD expertise- The ability to perform a range of structural calculations- Offshore Oil and#38; Gas/ Structural Design Experience- Degree in Mechanical Engineering- Enthusiasm/ Self-motivation/ Professionalism- A proven track record of successful project completionIf you feel you fit the outlined profile then I want to hear from you!Applications will not be considered after 5.00pm on the 25/04/2012. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Test and Validation Engineer  Brighton  Circa £33,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob59F70E0633AAA874482579F5001BAFB2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Test-and-Validation-Engineer-Brighton-Circa-and-amp-SHARP16333000_1638594.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for a Test and Validation Engineer to work for my client based in Brighton. Salary circa and#163;33,000.This role is to work alongside their Development team, to produce detailed and thorough product test specifications, both hardware (functional and environmental) and software.They are seeking an individual who can be creative, and discover how to make their products not work, by using the products as their customers do and then go beyond the specification to test the limits of the products.You will be involved in the steps required to help their products reach an exceptional level of reliability and usability.Requirements:and#149;Have an engineering degreeand#149;Experience of working on testing equipment and#150; Bench Testingand#149;Experience of using equipment as the user and#150; RTMand#149;It would be ideal if you have experience in Industrial or Temperature controllers]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Global Automotive  Rubery]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob509146AB43DF2A54482579F5001BAFC0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-and-amp-SHARP150-Global-Automotive-Rubery_1638595.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is proud to be working with an absolute key player in the Automotive industry with over a billion pounds worth of sales and an extremely positive outlook for 2012. The opportunity has come available for a new Quality Engineer at their Rubery site. This is an excellent chance to join a truly global company with a presence in over 20 countries which can offer long term career satisfaction and progression. As Quality Engineer you will be part of a strong team managing all Quality on site. This is a key role within the business and a real chance to prove yourself in a role.Interested? We are looking for some of the Quality Engineers in the Automotive industry. You must come from an Automotive background and have at least 2 years experience in a similar role. Most importantly though you must be up for the challenge of a life changing career change. On offer for the role is a starting salary of circa and#163;35,000 which is flexible dependant on the successful candidates skills and experience. There is also a generous benefits package. This is an urgent role with shortlisting occurring now so if you would like to be considered please apply online asap to Brooke Whitehead at Huxley Associates in order to avoid disappointment. NB This role may be suitable for, but is not limited to, the following job titles: Senior Quality Engineer, Quality Engineer, Quality Manager This role is commutable from: Rubery, Bromsgrove, Stourbridge, Redditch, Smethwick, Birmingham, Kiddeminster, Worcester, West Midlands, Worcestershire, Midlands.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer  Global Automotive Tier 1]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD20B74758937F41C482579F5001BAFDE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Quality-Engineer-and-amp-SHARP150-Global-Automotive-Tier-1_1638597.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is proud to be working with an absolute key player in the Automotive industry with over a billion pounds worth of sales and an extremely positive outlook for 2012. The opportunity has come available for a new Senior Quality Engineer at their Solihull site. This is an excellent chance to join a truly global company with a presence in over 20 countries which can offer long term career satisfaction and progression. As Senior Quality Engineer you will be part of a strong team managing all Quality on site. This is a key role within the business and a real chance to prove yourself in a role.Interested? We are looking for some of the Senior Quality Engineers in the Automotive industry. You must come from an Automotive background and have at least 2 years experience in a similar role. Most importantly though you must be up for the challenge of a life changing career change. On offer for the role is a starting salary of circa and#163;40,000 which is flexible dependant on the successful candidates skills and experience. There is also a generous benefits package. This is an urgent role with shortlisting occurring now so if you would like to be considered please apply online asap to Brooke Whitehead at Huxley Associates in order to avoid disappointment. NB This role may be suitable for, but is not limited to, the following job titles: Senior Quality Engineer, Quality Engineer, Quality Manager This role is commutable from: Birmingham, Stourbridge, Redditch, Kidderminster, Worcestershire, Warwickshire, Coventry, Solihull, Leicestershire, Derbyshire, West Midlands, East Midlands.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Autodesk Inventor Design Engineer, 6 Months, Leicestershire, 6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9B064B26ACB68DE9482579F5001BAFEA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Autodesk-Inventor-Design-Engineer-6-Months-Leicestershire-6-Months_1638598.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Autodesk Inventor Design Engineer, 6 Months, Leicestershire, 6 MonthsMy Leicestershire based client is currently recruiting for a Autodesk Inventor Design Engineer for a 6 month contract. I have summarised the role below. If this is of interest to you please forward me your most recent CV and I will contact you directly. Role: The project is to design and develop a retractable seating system, working with concepts through to detailed design, including structural analysis to ensure that all solutions are optimised and adhere to the standards and regulations required. The project will be taken from the concept stage through to prototyping, testing and the required certification to launch. Experience: and#149; Autodesk Inventor (essential) and#149; Confirming viability of structural members (including box steel structures, cantilevers and#38; cold rolled steel) and#149; Knowledge of motor driven systems and#149; Understanding of electronics]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Team Leader  Berkshire  £45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF2364FA6086CB6CB482579F5001BAFF9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Team-Leader-and-amp-SHARP150-Berkshire-and-amp-SHARP16345000_1638599.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[The Client: A leading Manufacturing Company who manufacturerand#146;s products for a vast range of Industries including Defence and Military Industries. The Person: and#149; Engineering Degree or equivalent (Mechanical or Electronics will be considered). and#149; Experience within the Defence Industry or any other structured industry and#149; 3D CAD designing and drafting or Solidworks and#149; Familiarity with electro-mechanical device design and manufacture. and#149; Experience of working with documentation change control systems (MTCB, FMECA). and#149; The ability to act as a bridge between mechanical and electronic disciplines and#149; Willing to go and#147;the extra mileand#148;, if necessary on short notice, in view of the fast turnaround nature of our business.  and#149; Experience of leading a team (project or department will be considered). Package: circa and#163;45,000 plus package. Apply: Please contact Akeela Tuffail on 0118 9565545 to apply for this vacancy and to discuss further or attach your CV through the apply link. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineering Team Leader  Berkshire  £45,0]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3EC361C27D325B79482579F5001BB008</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineering-Team-Leader-and-amp-SHARP150-Berkshire-and-amp-SHARP163450_1638600.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[The Client: A leading Manufacturing Company who manufacturerand#146;s products for a vast range of Industries including Defence and Military Industries. The Person: and#149;Engineering Degree or equivalent  (Mechanical or Electronics will be considered).and#149;Experience within the Defence Industry or any other structured industryand#149;3D CAD designing and drafting or Solidworksand#149;Familiarity with electro-mechanical device design and manufacture.and#149;The ability to act as a bridge between mechanical and electronic disciplines and#149;Experience and knowelge of Electrical components - PCB etcand#149;Knowledge of surface treatment  - casting, moulding, machining, finishingand#149;Experience of leading a team (project or department will be considered).Package: circa and#163;45,000 plus package. To Apply: Please contact Akeela Tuffail on 0118 9565545 to apply for this vacancy and to discuss further or attach your CV through the apply link.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Slough  £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob51DEC0AFD7468D25482579F5001BB022</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Slough-and-amp-SHARP16335000_1638601.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A global manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Slough office your main responsibilities are:and#149;Implement change orders to existing drawingsand#149;BoMs and documentationand#149;Liaise with other departmentsand#149;Ensure data packs are comprehensive, error-free and suitable for release to productionand#149;Work to Company procedures and standards, monitoring their effectiveness and proposing changes for improvement.and#149;Understand the complete range of products to provide comprehensive support service to the Group companies.Experience:and#149;2D/3D CAD (ProE preferred)and#149;Engineering change procedures in ISO9001 environmentThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.You will benefit from a salary from and#163;30,000 - and#163;35,000. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Commercial manager for Tidal device manufacturer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01FA7EA17E452696482579F5001BB02F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Commercial-manager-for-Tidal-device-manufacturer_1638602.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[An exciting new opportunity has recently became available within a leading tidal stream device manufacturer to represent them in the UK as a commercial manager. The company have ambitious plans to grow and become a leading developer in the tidal energy sector and have recently secured a large order for their equipment to be used for commercial applications.The role itself will involve representing the company into the UK market and will involve contacting developers, contractors, DNOand#146;s and consultancies and arranging meetings with them to discuss the companies exciting technology. You will be responsible for all project development and will be expected to manage the process from its inception. The ideal candidate will have a background in engineering and will be experienced in project management and development. It is required that the candidate has contacts within the DNOand#146;s and utility companies and will have experience working in Scotland, as this is the main target market for the company. It is preferable that the candidate has experience in the renewable sector and Wind and/or Wave experience will be a distinct advantage.In return you will be given the opportunity to join a rapidly expanding company and will receive a competitive salary along with bonus and package. If this is the type of challenge you are currently looking for then please apply at the earliest convenience to discuss this in more detail.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Slough  £30,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob321D8C67D0475CFC482579F5001BB03D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Slough-and-amp-SHARP16330000_1638603.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A global manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Slough office your main responsibilities are:and#149;Implement change orders to existing drawingsand#149;BoMs and documentationand#149;Liaise with other departmentsand#149;Ensure data packs are comprehensive, error-free and suitable for release to productionand#149;Work to Company procedures and standards, monitoring their effectiveness and proposing changes for improvement.and#149;Understand the complete range of products to provide comprehensive support service to the Group companies.Experience:and#149;2D/3D CAD (ProE preferred)and#149;Engineering change procedures in ISO9001 environmentThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.You will benefit from a salary from and#163;30,000 - and#163;35,000. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior CAD Draughtsman  Slough  £35,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD683B8F87F9D13CD482579F5001BB055</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-CAD-Draughtsman-Slough-and-amp-SHARP16335000_1638604.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A global manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Slough office your main responsibilities are:and#149;Implement change orders to existing drawingsand#149;BoMs and documentationand#149;Liaise with other departmentsand#149;Ensure data packs are comprehensive, error-free and suitable for release to productionand#149;Work to Company procedures and standards, monitoring their effectiveness and proposing changes for improvement.and#149;Understand the complete range of products to provide comprehensive support service to the Group companies.Experience:and#149;2D/3D CAD (ProE preferred)and#149;Engineering change procedures in ISO9001 environmentThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.You will benefit from a salary from and#163;30,000 - and#163;35,000. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior CAD Draughtsman  Slough  £30,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4B0E85A15FD6425E482579F5001BB064</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-CAD-Draughtsman-Slough-and-amp-SHARP16330000_1638605.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A global manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Slough office your main responsibilities are:and#149;Implement change orders to existing drawingsand#149;BoMs and documentationand#149;Liaise with other departmentsand#149;Ensure data packs are comprehensive, error-free and suitable for release to productionand#149;Work to Company procedures and standards, monitoring their effectiveness and proposing changes for improvement.and#149;Understand the complete range of products to provide comprehensive support service to the Group companies.Experience:and#149;2D/3D CAD (ProE preferred)and#149;Engineering change procedures in ISO9001 environmentThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.You will benefit from a salary from and#163;30,000 - and#163;35,000. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply chain coordinator, regio Adam]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1378AA227516AE74482579F5001BB072</referencenumber>
<City><![CDATA[Amsterdam]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supply-chain-coordinator-regio-Adam_1638606.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een toonaangevend bedrijf in de sports/fashion branche, zijn we op zoek naar een supply chain coordinator. De functieAls coordinator  ben je verantwoordelijk voor het managen van de inbound flow and#38; de inventory control van de producten. Je  begeleidt het gehele planning-proces. Ook zal je veel kennis opdoen van demand- en supply planning,  aangezien je als coordinator getraind zal worden om in te kunnen vallen voor de demand planners wanneer deze afwezig zijn. Als supply chain coordinator maak je deel uit van het Demand and#38; Supply planning team. Je rapporteert direct aan de Supply Chain Manager. Als  coordinator draag je verantwoordelijkheden voor werkzaamheden op verschillende gebieden, te weten: inbound logistiek, productie, inventory management and#38; demand planning. Je maakt rapporages and#38; planningen, en weet resultaten van bevindingen goed te communiceren/presenteren naar de verschillende afdelingen.  De functie-eisenMin. MBO+ HBO opleiding, aangevuld door 2-3 jaarwerkervaring in een soortgelijke functie. Kennis van ERP (SAP is een pre).Je bent communicatief and#38; analytisch sterk. Je bent ambitieus and#38; beheerst de Engelse taal uitstekend.Geinteresseerd? Stuur direct je cv + motivatie via onderstaande link. Voor meer informatie kunt u ook bellen naar Sanne Wissels: 020 522 1333.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA5344B8CCEEBFA59482579F5001BB08A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electrical-Design-Engineer_1638607.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Electrical Engineer - 6 month contract - Pontypridd. The client specialises in the design and manufacture of industrial control systems. Electrical Engineer will ideally have previous experience with the following:-Previous overhead and dockside crane experience.-Hands on experience with AC/DC motors, motor drives, PLC programming and relay logic.-EPLAN.Role:-Designing systems and products.-Reading design specifications and technical drawings.-Designing and conducting tests.-Qualifying the final product or system. -Commissioning equipment on site.If you are interested in a new contract opportunity please apply immediately to avoid missing out. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Gezocht: Planners  Merchandisers met RetailFashi]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob56CEA4BB16EE1E9F482579F5001BB0A1</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Gezocht:-Planners-Merchandisers-met-Retail-Fashi_1638608.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor verschillende retailers uit de fashion branche ben ik op zoek naar planners / merchandisers met ervaring.Ben jij minimaal HBO opgeleid? Heb je ervaring binnen de retail/fashion als planner/allocator/merchandiser? Ervaring met ERP-systemen en Excell? En ben je op zoek naar een nieuwe uitdaging? Reageer dan nu! Voor verschillende klanten in de regio Amsterdam, Utrecht and#38; Maastricht ben ik op zoek naar kandidaten met dit profiel.Geinteresseerd en voldoe je aan bovenstaande eisen? Reageer dan direct via onderstaande link met een up-to-date cv of bel t.a.v. Sanne Wissels en dan bespreken we de mogelijkheden. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Reliability Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0E0EA12F307FC96A482579F5001BB0AF</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Reliability-Engineer_1638609.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Reliability EngineerType functie: fulltimeBranche: ChemieLocatie: RotterdamVoor een chemisch bedrijf in de regio Rotterdam is Huxley Asssociates urgent op zoek naar een Reliability Engineer.Taken en verantwoordelijkheden:-  Je bent verantwoordelijk voor het realiseren van een hoge betrouwbaarheid van de installaties- Je zorgt voor het opstellen en optimaliseren van het preventieve onderhoudsprogramma van de installaties en productieprocessen met als doel de betrouwbaarheid te verhogen en de kosten te verlagen- Je waarborgt de technische kwaliteit van alle installaties en productieprocessen en verbetert de fabrieksperformance- Je maakt kritische analyses (FMECA studies) en storingsanalyses- Je bepaalt critical en capital spare parts- Je initieand#235;rt restlevensduurstudies - Je werkt mee aan de realisatie van verbeterplannen en projectenProfiel:- Diploma wertktuigbouwkunde  (Mechanical Engineering) - Minimaal 5 -10 jaar werkervaring; - Kennis van GMP en EHS; - Ervaring met het opstellen van onderhoudsprogrammaand#146;s en RE analyses (RCM, Six Sigma en TPM) Interesse? Reageer dan nu ter attentie van Daniel de Keyzer van Huxley Associates via de aangegeven link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Reliability Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFD2F69EF0513DF18482579F5001BB0BE</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Reliability-Engineer_1638610.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Reliability EngineerType functie: fulltimeBranche: ChemieLocatie: RotterdamVoor een chemisch bedrijf in de regio Rotterdam is Huxley Asssociates urgent op zoek naar een Reliability Engineer.Taken en verantwoordelijkheden:-  Je bent verantwoordelijk voor het realiseren van een hoge betrouwbaarheid van de installaties- Je zorgt voor het opstellen en optimaliseren van het preventieve onderhoudsprogramma van de installaties en productieprocessen met als doel de betrouwbaarheid te verhogen en de kosten te verlagen- Je waarborgt de technische kwaliteit van alle installaties en productieprocessen en verbetert de fabrieksperformance- Je maakt kritische analyses (FMECA studies) en storingsanalyses- Je bepaalt critical en capital spare parts- Je initieand#235;rt restlevensduurstudies - Je werkt mee aan de realisatie van verbeterplannen en projectenProfiel:- Diploma wertktuigbouwkunde  (Mechanical Engineering) - Minimaal 3 jaar werkervaring; - Kennis van GMP en EHS; - Ervaring met het opstellen van onderhoudsprogrammaand#146;s en RE analyses (RCM, Six Sigma en TPM) Interesse? Reageer dan nu ter attentie van Daniel de Keyzer van Huxley Associates via de aangegeven link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CONTRACTINDUSTRIALISATION EXPERT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3A53D3DF52101AE3482579F5001BB0CB</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/-CONTRACT-INDUSTRIALISATION-EXPERT-_1638611.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A hertfordshire based client is looking for an Industrialisation/Manufacturing Engineer, the candidates will need to be highly experienced in the medical devices and pharmaceutical industry and they need to be proficient in:Injection MouldingAssembly LinesValidation and QualificationManufacturing DesignHandling ISO Documents, reviewing reportsPlease apply immediately to avoid missing out the chance to work alongside a group of talented individuals for a well known client in the Pharmaceutical Industry. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Wind Farm Civils Site Manager  Scotland  6 month]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0CA79945FA436C30482579F5001BB0DD</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Wind-Farm-Civils-Site-Manager-Scotland-6-month_1638612.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Wind Farm Civils Site Manager - Scotland - 6 monthA client of ours has contacted me with regards to an opening they have for the above. They have won a contract to erect 5 turbines and are so looking for someone who has previous experience of Wind Farm builds. The RoleOversee the Laying of Access RoadsBuilding Controls BuildingInstallation of the Bases of the TurbinesDesirableSubstation Build ExperienceIf you have this experience and you are interested in the role please get in touch to discuss things in more detail. I look forward to hearing from you. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Solidworks  Medical Device]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0DFD88DC2EEA8A2F482579F5001BB0ED</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Solidworks-Medical-Device_1638613.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[have an exciting opportunity to join a manufacturing company in the Gloucestershire area who operate within the Medical Device market. They are looking for a Mechanical Design Engineer to join their growing team. Skills Sought: -Good Analytical Skills -An understanding of injection moulding tooling and manufacturing methodologies. -A good understanding of CAD and#38; PDM systems (SolidWorks) functionality would be an advantage. -Min 1 years experience If you have any exposure to Quality Management Systems (ISO) this would be highly desirable.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Opportunity to move to a Project Engineer role]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF2CF5E060461B803482579F5001BB0F9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Opportunity-to-move-to-a-Project-Engineer-role_1638614.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Project Engineer and#150; Gloucestershire to and#163;35,000Huxley Associates are working with a large multinational organisation in Gloucestershire to recruit a Project Engineer to add to a successful team. You could have come from mechanical engineering background and want to move to the next step. Job Details:The key responsibilities are to project manage (NPI) new product introduction by bringing together all aspects of engineering to successfully deliver the finished product.ExperienceThe main attributes to be seen on a CV are the following:-Experience within a mechanical environment-Ideally experience with NPI-Ability to work in a multi-cross functional teamYou may have experience in the following roles:  Mechanical engineer Project Engineer, Project Leader, Senior Project EngineerSalary: to and#163;35,000If this is of interest or you know someone who is looking please forward me a copy of your most recent CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD81CF2D64ADCCCB4482579F5001BB104</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager_1638615.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is looking for a Procurement Manager to join their team during an exciting period of growth. This role is an excellent opportunity to work for a leading energy company with a Global presence. The successful candidate will: Be involved with Category Management and Strategic Sourcing alongside operational procurementHave experience with IT or Category ManagementLead contract negotiation on high value, business critical contractsEnsure strong management of commercial activitiesEnsure that all contracts are to the highest qualityEnsure that contracts reduce the risk, whilst ensuring delivery of OTDDevelop sourcing strategy for key technology and servicesCreate supplier information sharing networksManage complete end-to-end sourcing process: From supply analysis, bid tender and through to writing contractsBe involved with resolving supplier/contract issue The successful candidate will benefit from a competitive salary of up to and#163;40,000 If you are interested in applying for this position please attach your CV and/or contact Becky Murphy on 01189 56 55 45. Closing date for this role is Wednesday 25th April. Please note that if you do not hear from us within 5 working days of application that, unfortunately, you have not been successful for this roleand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ElectroMechanical Design Engineer  £50,000  Benefits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB664A8F0FBF14453482579F5001BB111</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Design-Engineer-and-amp-SHARP16350000-Benefits_1638617.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Essex office you will be reporting to the Engineering Manager and will be responsible for the full product life cycle to assist with rapidly increasing demand.Experience:and#149;Mechanical Engineering Qualification (HNC/Degree)and#149;Thermal Analysis/CFD/CoolingThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.They will benefit from a highly competitive salary. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Embedded Engineer  Oxfordshire  Fantastic Package]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob55F1775FE9569FC9482579F5001BB122</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Embedded-Engineer-Oxfordshire-Fantastic-Package_1638618.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently recruiting for a number of Embedded Engineerand#146;s to join my client based in Oxfordshire who offer a fantastic salary and benefits package.My client has built on its expertise in highand#38;#8208;speed memory to become a dominant player in the manufacturing and distribution of solid state drives (SSDs).The key to being a successful candidate for this role is to be a good problem solver. Without this you will not be considered.You would have also been in positions which involve you talking down to the registers. Technical experience to includeand#38;#8208;and#38;#8208; Extensive experience in C and/or Assembler - Experience in Embedded environmentsand#38;#8208; Experience with ARM OR Cortex The following will also be desirable:and#38;#8208; Software design (preferably using UML)and#38;#8208; Experience of Software testing- Experience and knowledge of multi-threading.Experience of working for any storage companies will be of great advantage.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ElectroMechanical Design Engineer  £45,000  Benefits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB26E1426F5448AAA482579F5001BB131</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Design-Engineer-and-amp-SHARP16345000-Benefits_1638619.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Essex office you will be reporting to the Engineering Manager and will be responsible for the full product life cycle to assist with rapidly increasing demand.Experience:and#149;Mechanical Engineering Qualification (HNC/Degree)and#149;Thermal Analysis/CFD/CoolingThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.They will benefit from a highly competitive salary. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Planner  Water Industry  East Midlands]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC07FC7DD4D757E49482579F5001BB141</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Planner-Water-Industry-East-Midlands_1638620.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently working with several large companies that are constantly working through the AMP periods.I am currently looking for a strong, hands on project planner with ample experience within the water industry to use MSP on several upcoming projects.All my roles are contract and I aim to deal with Minimum 6 month contracts.If you have:* Water/ waste water/ clean water/ sewage/ sludge experience.* Primavera, P3, P3E, P5, P6, MSP (Microsoft Project)* Site experience* Good interpersonal skillsIf you want to be part of the growing companies, with lucrative packages, please send me your CV as soon as possible.I am currently looking for an experienced MSP Project Planner for the East Midlands.Please contact me immediately if you are interested. Over the next few months I will have many planning positions within the water industry coming available and I would like to hear from you if you have the relevant experience and are looking for a new challenging role.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Motors  up to £35k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob606091AC21D843CE482579F5001BB14E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Motors-up-to-and-amp-SHARP16335k_1638621.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am working with a successful manufacturing company based in Swindon who are part of a wider and#163;100m turnover group and are now looking for an Electromechanical Design Engineer. The company has a strong pipeline of work and opportunity for rapid expansion so therefore it will be great time to join and to enjoy career progression. In this role you will be working on the development of air movement products for general and bespoke requirements. Ideal Skills Sought: -Electro Mechanical Design Background -Sheet Metal Product Design -Product testing, approval and documentation -Reliability and failure mode analysis -CAD for electromechanical design My client would be interested in you if you have skills in:-- Motor Design- Rotating Machinery- Air Compression / Expansion- CastingsIt would be highly desirable if you have experience in design for air flow products.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ElectroMechanical Design Engineer  £35,000  Benefits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6350F79A2BC334E8482579F5001BB15C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Design-Engineer-and-amp-SHARP16335000-Benefits_1638622.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Essex office you will be reporting to the Engineering Manager and will be responsible for the full product life cycle to assist with rapidly increasing demand.Experience:and#149;Mechanical Engineering Qualification (HNC/Degree)and#149;Thermal Analysis/CFD/CoolingThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.They will benefit from a highly competitive salary. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electro Mechanical Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5E92F0E8733A94F0482579F5001BB181</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Design-Engineer_1638624.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am working with a successful manufacturing company based in Swindon who are part of a wider and#163;100m turnover group and are now looking for an Electromechanical Design Engineer.The company has a strong pipeline of work and opportunity for rapid expansion so therefore it will be great time to join and to enjoy career progression.In this role you will be working on the development of air movement products for general and bespoke requirements. Ideal Skills Sought:-Electro Mechanical Design Background-Sheet Metal Product Design-Product testing, approval and documentation-Reliability and failure mode analysis-CAD for electromechanical designIt would be highly desirable if you have experience in design for air flow products.Please apply here for a swift response and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ElectroMechanical Design Engineer  £30,000  Benefits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8F7D9EA9C11AD9D7482579F5001BB190</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electro-Mechanical-Design-Engineer-and-amp-SHARP16330000-Benefits_1638625.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading manufacturer is currently looking to recruit a Mechanical Design Engineer to add to their highly successful team. Based in the Essex office you will be reporting to the Engineering Manager and will be responsible for the full product life cycle to assist with rapidly increasing demand.Experience:and#149;Mechanical Engineering Qualification (HNC/Degree)and#149;Thermal Analysis/CFD/CoolingThey are looking for someone who is an independent, self-starter with strong leadership qualities for future lead design opportunities.They will benefit from a highly competitive salary. To apply, please attach your CV and/or call Ehsan Khan on 01189 56 55 45.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Buyer  Thames Valley  6  12 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB386DBD03B23F7AB482579F5001BB1A1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Buyer-Thames-Valley-6-12-Months_1638626.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My Client looking for an Interim Senior Buyer to join their purchasing team in the Thames Vally, during a very busy period of business.Key responsibilities include:and#149;Risk assessment to discover external supply risk from supplier selection through to contract execution and management.and#149;Using knowledge of commercial contract law to develop and sign off contractual terms and conditionsand#149;Leading commercial / contractual discussions with suppliersand#149;Identifies, implements and realizes value through effective and#145;strategic cost managementand#146; utilizing best practise methods and tools and evaluates business risk through ensuring rigorous contract management controlsand#149;Routinely communicates to key business stakeholders to ensure alignment of the Supply Chain and the internal customer Requirements:and#149;Experience required in standard Supply Chain Managementand#149;Systems and tools in project performance and category management.and#149;Previous experience in Engineering industry (in Civil Engineering would be preferable)and#149;Ability to work proactively with minimum supervisionand#149;Ability to set and meet own objectives and deadlinesand#149;Good teamwork skills and experience of working in multi-discipline and multi-company teamsand#149;High level of self-motivation and enthusiasmand#149;Track record of delivery in a project environmentand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Design Engineer  Solidworks  Cornwall]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob29ABB039B186EB73482579F5001BB1AE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Design-Engineer-Solidworks-Cornwall_1638627.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Design Engineer and#150; Solidworks and#150; Cornwall and#150; 6 Month ContractHuxley Associates are currently looking for a contract Design Engineer for a 6 Month contract in Cornwall.The candidate will be joining the existing design team and assist with the development of conceptual design and engineering calculations. Also they will be produce detailed design drawings for fabrications and machined parts.Day to Day Roles:Production of conceptual design schemes in 2D and 3D.and#149; Production of detailed design schemes in 2D and 3D.and#149; Production of detailed engineering hand calculations and FE analysis.and#149; Production and submission of 3rd party design verification reports.and#149; Production of detailed 2D engineering drawings for manufacture.and#149; Participate in regular formal design reviews as required.and#149; Creation and adherence to project schedules as required Essential Skills: Qualified to Degree/HND level.and#149; Minimum of 5 years experience in heavy engineering, preferably drilling related.and#149; Proficient in the use of SolidWorks 3D design package.and#149; Proficient in the use of AutoCAD 2D for conceptual design set outs.and#149; Preferably familiar and proficient with Staad Pro.and#149; Proficient in the production of hand calculations.and#149; Familiar in the use of engineering analysis software, preferably SolidWorks Simulation.and#149; Computer literate in Microsoft office suite.and#149; Display good time keeping.and#149; Display a willingness to integrate and work within a team.Location: CornwallDuration: 6 MonthsRate: Marketand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Development Manager up to 80k  Bonus]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob013937488AD80F3A482579F5001BB1BC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Development-Manager-up-to-80k-Bonus_1638628.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[How would you like to be part of a Business who are looking to Double their turnover in the next 3 years?Interested?Due to the MDand#146;s entrepreneurial approach, mergers and acquisitions and a passion for customer service and innovation they company are now looking for a Senior Business Development manager with a view to becoming a Director after a short period.Operating in a niche market my client is a highly successful Technical Outsourcing Support Company. Your role will be to define Market strategies and client relationships. Development of new pipeline business and management of existing Outsourced business. Your role is to ultimately help with the aggressive growth plans to Double in Size over the next 3 years.You will also work with the Internal/External Channel team and resellers to develop and improve marketing activities.The candidate will have a proven track record in developing new business within a Technology environment and be able to act upon market intelligence and identify new strategic partnerships. You will also have experience of operating at Senior level and be able to influence the development of the strategic agenda alongside the MD and Non Execs.Experience of Mergers and Acquisitions would also be desirable but is not essential. International experience would also be desirable.Degree would also be desirable.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement Manager  Gloucester  12 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD6EA732F151AAB24482579F5001BB1CA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager-Gloucester-12-Months_1638629.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A leading Engineering company is looking to take on an Interim Procurement Manager to oversee the entire procurement process during a busy period of business.They will primarily be responsible for:and#149; Strategic process planning, including warehousing and distributionand#149; Overseeing strategy with suppliers with the focus on building long term relationshipsand#149; monitor and delegate the supporting team of buyersand#149; Strategic Sourcingand#149; Development of long term supply and service contractsand#149; Inventory decisions, including quantity, location, and quality of inventoryand#149; Benchmarking of all operations against competitors and implementation of best practiceand#149; Organizing department effectively to ensure satisfaction of internal and external suppliers and customersand#149; Manage vendor purchase order issuance and executionand#149; Receive, track, review and/or approve required vendor document submittals utilizing document control processes and procedures This will be a 12 month interim position with the possibility to go permanent.Please send me your up to date CV and if you are sucessful I will give you a call back to discuss the role further.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Manager  Aerospace Solutions Sales  £45k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5D839C34D29AB145482579F5001BB1D7</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Manager-Aerospace-Solutions-Sales-and-amp-SHARP16345k_1638631.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Sales ManagerAerospace Solutions Sales Manufacturer of Gears, Gearboxes and Power Transmission Products South East or Midlands Based Key Customers like BAE Systems, Goodrich and MOD.and#163;45,000 basic plus bonus and packageAn excellent opportunity for a Sales Manager from the Aerospace and Defence sector to join a leading UK manufacturer of gears, gearboxes and power transmission products. For this role industry experience is more essential than product experience, so it isnand#146;t essential that you will have sold gears of gearboxes but what is essential is that you have proven sales experience selling solutions (not box shift/off the shelf products) into the Aerospace and Defence sector.Typical key clients are organisations such as BAE Systems, Goodrich and the MOD. So previous experience selling into these or similar organisations is required. Due to the location of the organisation and their key customers, we are seeking a Sales Manager who is either based in the South East or the Midlands.For the successful candidate the anticipated remuneration will be a basic of and#163;45,000 plus car package, bonus and usual tools of the trade. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Process Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD56884F0E41D8DE3482579F5001BB225</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Process-Engineer_1638636.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Process EngineerBranche: Chemie (Plastic)Locatie: Zuid-HollandSalaris: 40-70kFulltimeBereid 50% internationaal te reizen Voor een internationaal gerenomeerd chemische bedrijf in de polymer industrie is Huxley Associates urgent op zoek naar een process engineer. Taken en verantwoordelijkheden:- Je  draagt zorg voor de benchmark van het productieproces tegen processen van de concurrentie- Je analyseert (zowel in -als externs) mogelijke verbeteringen (inclusief uitbreidingen) van het productieproces - Je bent bekend op het gebeid van Rand#38;D wanneer het gaat om de proces ontwikkeling - Je bent bereid tot 50% internationaal te reizen voor het beantwoorden van vaktechnische vragen van klanten.  Profiel:- HBO/WO werk-en denkniveau richting chemie- Minimaal 3 jaar ervaring in de productie- Kennis van polymeren is een enorme pre - Uitstekende beheersing van de Nederlandse en Engels taal in woord en geschrift (een derde taal is een pre)- Communicatief vaardigInteresse? Stuur dan je CV naar Daniel de Keyzer van Huxley Associates via de onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Process Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA1C13E7C6F64C332482579F5001BB244</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Process-Engineer_1638638.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Functie: Process EngineerBranche: Chemie (Plastic)Locatie: Zuid-HollandSalaris: 50-70kFulltimeBereid 50% internationaal te reizen Voor een internationaal gerenomeerd chemische bedrijf in de polymer industrie is Huxley Associates urgent op zoek naar een process engineer. Taken en verantwoordelijkheden:- Je  draagt zorg voor de benchmark van het productieproces tegen processen van de concurrentie- Je analyseert (zowel in -als externs) mogelijke verbeteringen (inclusief uitbreidingen) van het productieproces - Je bent bekend op het gebeid van Rand#38;D wanneer het gaat om de proces ontwikkeling - Je bent bereid tot 50% internationaal te reizen voor het beantwoorden van vaktechnische vragen van klanten.  Profiel:- HBO/WO werk-en denkniveau richting chemie- Minimaal 3 jaar ervaring in de productie- Kennis van polymeren is een enorme pre - Uitstekende beheersing van de Nederlandse en Engels taal in woord en geschrift (een derde taal is een pre)- Communicatief vaardigInteresse? Stuur dan je CV naar Daniel de Keyzer van Huxley Associates via de onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lean Manufacturing Best Practice Consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4794B0F2C7B6AA72482579F5001BBD4F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lean-Manufacturing-Best-Practice-Consultant_1642727.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Manufacturing organisation based in the North West is currently recruiting for a Best Practice Lean Consultant who is available for a 9 month interim assignment. The company in question are an international organisation and this role will see the successful manager spend most of their time at various sites across Europe.Your role will be to ensure the development and implementation of best practice procedures across the companies various sites. You will be responsible for project management, process improvement and training with a focus on ensuring that projects come in on time and to budget.You will play in active part in key decision making, identifying areas for improvement, problem solving and eliminating waste. The successful candidate will have a track record either as a process improvement specialist or operations manager and will have performed roles that incorporate both a strategic and practical element. You will have an expert knowledge of the lean manufacturing tool set as well has a sound understanding of the principals behind Six Sigma.This is an exciting opportunity for a skill consultant who is flexible with regards to location. Please apply for further information.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Operations Manager  Nottingham  £50000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB9FA9310E9A90EB2482579F5001BBD65</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Operations-Manager-Nottingham-and-amp-SHARP16350000_1642728.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is pleased to be working alongside one of the leading Manufacturers within FMCG, with a circa and#163;10 million turnover. They are looking for someone to head up all Operations at their Nottingham site.As Operations Manager you will have full responsibility for all staff on site which requires proven man management skills. You will be responsible for Production, Logistics, Purchasing and all other Operations. This requires driving productivity and efficiency and managing day to day manufacturing. What is exciting about this opportunity is that the company wants to go to the next level, allowing the right candidate to establish an exceptional career. The starting salary is circa and#163;50,000 + Car + Health insurance + 5% bonus. This is also flexible dependant on the successful candidatesand#146; skills and experience.This is an urgent role with shortlisting occurring now so if you would like to be considered please apply online to Azeem Jabar at Huxley Associates ASAP in order to avoid disappointment. NB This role may be suitable for, but is not limited to, the following job titles: Operations Manager, Production Manager, Manufacturing Manager, Site ManagerThis role is commutable from: Derby, Birmingham, Loughborough, Birmingham, Coventry, Leicestershire, Derbyshire, West Midlands, East Midlands.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Product Design Role Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob38862227CD8FE938482579F5001BBD72</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Product-Design-Role-Bath-and-amp-SHARP16340000_1644808.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a senior product design engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Design Engineer Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4F36BF88AC393707482579F5001BBD7F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Design-Engineer-Bath-and-amp-SHARP16340000_1644809.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a product design engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Solidworks Engineer Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF4D82B7B3EFAC8A4482579F5001BBD95</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Solidworks-Engineer-Bath-and-amp-SHARP16340000_1644810.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a Solidworks engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Planner  Pembroke  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF756AE8099A113E4482579F5001BBDA5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Planner-Pembroke-Contract_1644811.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley are looking for Planning and#38; Scheduling Engineers  associated with Oil and#38; Gas (LNG/Refineries/Petrochemical Plants/CCGT Power stations) This will be a long contract based in Pembroke. Candidates must have the following expereince:Planning and#38; Scheduling, Earned value Analysis. Reporting: S-curves, Tabular, Slippage, Man power/Qty histograms Risk Analysis/ Crash schedules development etc Shutdowns/Turnarounds EPC Projects: Civil/Structural/Mand#38;E (Piping, Elec and#38; Instrumentation) and Commissioning and#38; FEED PROJECTS Offshore Assets Management Planning etc (North Sea) NEC contracts awareness and#38; Cost Control, EHS  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEF9C7B9D42788A39482579F5001BBDBF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Bath-and-amp-SHARP16340000_1644812.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a senior mechanical design engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Product Design Role Bath £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF3F2975C286227E4482579F5001BBDD2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Product-Design-Role-Bath-and-amp-SHARP16340000_1644813.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client based in Bath has an urgent need for a senior product design engineer on a permanent basis.My client works to produce specialist equipment for the petro-chemical, oil, and gas industry.Due to a number of projects the company require additional resource to join their already large design team.This is an exciting opportunity for the right candidate to be solely working on new product design.Key Skills:and#149;Solidworks, Pro-Engineerand#149;Formal qualification in mechanical engineeringDesirable Skills:and#149;Experience of working with pressure vessels, valves, fluid flow/flow analysis, precision engineeringand#149;Structural calculations - experience using FEA, MathCAD etc.Location: BathSalary: and#163;40,000Please send your CV in now for immediate consideration, this is an immediate requirement. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Product Development Newport £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7C76F515BAF7A4F7482579F5001BBDE1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Product-Development-Newport-and-amp-SHARP16340000_1651572.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is one of the worldand#146;s largest producers of Design radiators based in South Wales. and#149;Degree or Equivalent in Mechanical Engineering and#149;Previous experience within a new product introduction role within a manufacturing facility and#149;A good understanding of a broad range of physical principles, particularly in relation to electrical, thermal, mechanical and optical disciplines. and#149;Experience in managing several project simultaneously as well as technical leadership and project planning. and#149;Negotiation and#38; consensus-building skills combined with the ability to present information clearly and concisely. and#149;Strong numeracy and data analysis skills as well as an ability to draw clear conclusions. and#149;Broad technical and logistical problem solving capabilities.Salary is on offer up to and#163;40,000 + benefits. If you feel you are a suitable match for this role- please send an up to date CV across.  As part of an exciting growth strategy, my client is looking to recruit a new product engineer r to further develop and manage the NPD process including market analysis and value proposition development.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Newport £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB68AAC99275EC84F482579F5001BBDEE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Newport-and-amp-SHARP16340000_1651573.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is one of the worldand#146;s largest producers of Design radiators based in South Wales. and#149;Degree or Equivalent in Mechanical Engineering and#149;Previous experience within a new product introduction role within a manufacturing facility and#149;A good understanding of a broad range of physical principles, particularly in relation to electrical, thermal, mechanical and optical disciplines. and#149;Experience in managing several project simultaneously as well as technical leadership and project planning. and#149;Negotiation and#38; consensus-building skills combined with the ability to present information clearly and concisely. and#149;Strong numeracy and data analysis skills as well as an ability to draw clear conclusions. and#149;Broad technical and logistical problem solving capabilities.Salary is on offer up to and#163;40,000 + benefits. If you feel you are a suitable match for this role- please send an up to date CV across.  As part of an exciting growth strategy, my client is looking to recruit a new product engineer r to further develop and manage the NPD process including market analysis and value proposition development.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[New Product Development Newport £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE5125AF5A5B66627482579F5001BBE04</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/New-Product-Development-Newport-and-amp-SHARP16340000_1651574.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is one of the worldand#146;s largest producers of Design radiators based in South Wales. and#149;Degree or Equivalent in Mechanical Engineering and#149;Previous experience within a new product introduction role within a manufacturing facility and#149;A good understanding of a broad range of physical principles, particularly in relation to electrical, thermal, mechanical and optical disciplines. and#149;Experience in managing several project simultaneously as well as technical leadership and project planning. and#149;Negotiation and#38; consensus-building skills combined with the ability to present information clearly and concisely. and#149;Strong numeracy and data analysis skills as well as an ability to draw clear conclusions. and#149;Broad technical and logistical problem solving capabilities.Salary is on offer up to and#163;40,000 + benefits. If you feel you are a suitable match for this role- please send an up to date CV across.  As part of an exciting growth strategy, my client is looking to recruit a new product engineer r to further develop and manage the NPD process including market analysis and value proposition development.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer Newport £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob392C61A71F196177482579F5001BBE10</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Newport-and-amp-SHARP16340000_1651577.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is one of the worldand#146;s largest producers of Design radiators based in South Wales. and#149;Degree or Equivalent in Mechanical Engineering and#149;Previous experience within a new product introduction role within a manufacturing facility and#149;A good understanding of a broad range of physical principles, particularly in relation to electrical, thermal, mechanical and optical disciplines. and#149;Experience in managing several project simultaneously as well as technical leadership and project planning. and#149;Negotiation and#38; consensus-building skills combined with the ability to present information clearly and concisely. and#149;Strong numeracy and data analysis skills as well as an ability to draw clear conclusions. and#149;Broad technical and logistical problem solving capabilities.Salary is on offer up to and#163;40,000 + benefits. If you feel you are a suitable match for this role- please send an up to date CV across.  As part of an exciting growth strategy, my client is looking to recruit a new product engineer r to further develop and manage the NPD process including market analysis and value proposition development.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Construction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electronic Engineer PCB Design Downhole Oil and Gas]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6DF3A5453CDCA63E482579F5001C0048</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Electronic-Engineer-PCB-Design-Downhole-Oil-and-Gas_1639553.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[OPPORTNITY FOR A SENIOR ELECTRONIC ENGINEER TO PROGRESS AND BUILD UP SALLARY- FUTURE MANAGEMENT OPPORTUNITYAre you looking for a new position with a large Oil and Gas Company in Aberdeen who are known internationally? I am currently looking for a Senior Electronics Engineer/ Designer to join an established and growing company in Aberdeen. They are looking for someone to come on board and grow within the company. This is an urgent requirement. On top of the progression available, this company pay one of the highest salaries in Aberdeen for people with this background. This is a fantastic opportunity. PLEASE APPLY NOW!.  The Roleand#149;The right candidate will play a key role in the design, development and testing of new data acquisition products as well as working on existing productsand#149;You will play a key role in the department and#149;Coaching/ ManagementThe PersonEssential:and#149;Design experienceand#149;Strong Electronic backgroundand#149;Microcontroller software development experienceand#149;PCB Design experienceDesirable:and#149;Electronics degree or similar disciplineand#149;High Temperature electronic design experience Unfortunately there is no funding available for sponsorship. If you are interested please send me your CV ASAP. Interviews will be taking place Friday this week and Monday next week. They are looking to get the right person on board as soon as possible.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior design engineerprojects staffAberdeen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC6937F615D039EA7482579F5001C0053</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-design-engineer-projects-staff-Aberdeen_1639554.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A well established Subsea service company based in Aberdeen is looking to bring on board a senior design engineer on a staff basis. This is a project based engineering position and you will be looking after international and UK projects. In this position you are likely to be looking at more than one project and you will be required to interact with other departments supply chain, project management and manufacturing.Day to day role:-Generate conceptual designs or customise existing designs for proposals and projects.-Verify design where necessary using classical analysis-Prepare design layouts-Present design to engineering staff during internal design reviews-Prepare DBIand#146;s and review details drawing-Generate equipment assembly, test, FAT, handling and storage ETCExperience:-oil and gas experience-Subsea tree and wellhead would be advantageous-Design engineering experience-Experience with project design-DegreeSalary: open at the momentIf you are interested in this position please send me an up to date CV today and I can discuss this position with you.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project lead engineer Staff Aberdeen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC759AC4CCE2EA9BC482579F5001C006C</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-lead-engineer-Staff-Aberdeen_1639556.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A well established Subsea service company based in Aberdeen is looking to bring on board a project lead engineer on a staff basis.They require someone to come and work on their international projects while supervising/managing other members of the team.You will be required to work on a number of projects and you will need to be able to demonstrate you have the skills in project processes and design processes.Day to day role:-Deliver equipment with compliance to specification-Control product design for projects (including design review/approval)-Raise ECR-Review of projects-Managing design engineers and senior design engineersExperience:-oil and gas experience-previous design experience-projects experience-basic supervisory experience-proven practical engineering experience-experience executing projectsSalary: open at the momentIf you are interested in this role please can you send me your up to date CV today and I look forward to discussing this with you.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electronic Engineer Downhole High Temperature Design]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF017F44CA8E2A154482579F5001C007B</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Electronic-Engineer-Downhole-High-Temperature-Design_1639557.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you looking for a new opportunity in the Oil and Gas industry in Aberdeen?I am currently looking for a Senior Electronic Engineer to join a Field Service Company in Aberdeen. This company is part of a large international group of companies who have offices world wide. They are expanding rapidly and they are looking an innovative career minded candidate to join the company and help steer it forward.The Role:and#149;80% of your time will be spent testing and designing new prototypesand#149;20% of your time will be spent on existing productsand#149;You will be working on High Temperature Design and working out which components can be usedand#149;Design will be a large part of this role as wellThe Person:and#149;High Temperature Electronics experienceand#149;PCB Designand#149;Microcontroller experienceand#149;Experience in a senior role This is a fantastic opportunity that does not come around very often. You will be one of the most senior people in the department. In return for your skills the company is offering a very competitive pay structure and benefits package as well as a bonus. Interviews will be taking place next week. If you are interested please send me an updated CV ASAP.Unfortunately there is no funding available for sponsorship.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager Control Systems DCS]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA6C5AC5BA40C41DF482579F5001C008A</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager-Control-Systems-DCS_1639558.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you looking for your next opportunity in the Oil and Gas Industry? I am currently looking for a Project Manager to work for a large Vendor in the Aberdeen area. This is a fantastic opportunity for someone to join an expanding company who is involved in a lot of interesting projects. This is an opportunity for someone with several years Project Management experience or someone who has very strong technical experience. The Role:and#149;Managing Projects from start to finish and#149;Managing Systems Engineers and Field Engineerand#149;Manage the finances of the Projectsand#149;Work with the Engineering Manager on Projectsand#149;Travel within the UK and internationally if required The Person:and#149;Either a strong technical background in Control Systems or a strong Project Management experienceand#149;Experience with Computer based control systemsThis company is dramatically expanding. They can offer progression, training and a good financial package to the right candidate.If you are interested please send me your CV ASAP. Kind Regards,]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ROV Sales Manager  Aberdeen  Negotiable]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2D0D57534BD9629E482579F5001C0096</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ROV-Sales-Manager-Aberdeen-Negotiable_1639559.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading provider of services to the subsea sector who are looking for a regional sales manager. The sales manager will be tasked with increasing revenue and margins from customers in the European and North Sea market place. The day to day activities of the role will include building long term relationships with key clients, identifying opportunities across the region for the company and ensuring that the company are on relevant bid lists for all major projects. Key Requirements: -Demonstrable sales track record within oil and gas industry-Product knowledge of ROVand#146;s-Excellent interpersonal skillsThe role comes with an excellent base salary and benefits package. Ideally the role will be located in Aberdeen but flexible arrangements will be considered for outstanding candidates.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Engineer C C# Very competative package]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBEEED2F9C87DC90F482579F5001C0218</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Engineer-C-C-SHARP-Very-competative-package_1642750.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Are you looking for a new position within the Oil and Gas industry?I am currently looking for a Software Engineer to join an Oil and Gas company in Aberdeen. This is for a rapidly expanding company who are looking for a Software Engineer to become an integral part of their team.The Roleand#149;Writing new Softwareand#149;Using C++and#149;C#and#149;Opportunity for travel if desiredThe Personand#149;Experience with C++ and C#and#149;Experience as a Software EngineerThis company are looking for people who are interested in the application of the Software and people who want to make a real contribution to a company and who is happy to effect change in a company. You will be integral to the growth of the company and in return for this there is a very competitive package on offer. If you are interested please apply now.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Development Manager  SubSaharan Africa]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob58DBC89EF4091B08482579F5001C0226</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Development-Manager-Sub-Saharan-Africa_1651621.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working  with a small company that specialise in innovative completion technology who are looking for a business development manager to drive growth in the Sub Saharan Africa Region. The company have had excellent growth in Europe and North America and are looking to emulate this success across other regions and this position is the first appointment as part of the companies ambitious growth plans. Candidates for the position should have technical knowledge of the completions sector coupled with a strong sales track record. Candidates will also have a strong understanding of the market dynamics for the region. The position offers an excellent opportunity for career progression. The role will naturally grow into a region manager position with Pand#38;L responsibility and longer term there will be multiple avenue to progress to executive level. The role comes with excellent salary and package with generous bonus. For more information please contact Thom Partridge at Huxley Associates]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer with Hydraulics Experience Required]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEE92E70CF9A1A757482579F5001C0234</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-with-Hydraulics-Experience-Required_1664325.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is looking for a Mechanical Engineer to join their Global Oil and Gas Service Company on a Staff basis in Aberdeen.The role is as follows:and#149;Experience: Relevant engineering and#149;Qualifications: Relevant Degree, HND or engineering experienceand#149;Subsea or Downhole experienceand#149;Landing String / Xmas Tree Knowledge preferableand#149;Design ExperienceoCarry out detail calculations (Pressure Vessel etc) to prove integrity of componentsoCreate / Review technical documentation and#150; Design specifications, Reports, Test ProceduresoRoot Cause AnalysisoDesign for ManufactureoKnowledge of engineering standards (API 6A, API 14A, ISO 13628-7) and practicesoCompetent in reviewing 2D and#38; 3D drawings for manufactureand#149;Engineering Database knowledge preferableand#149;Able to use AutoCad, Inventor and MathCadand#149;Computer LiterateIf you are looking for a new role please get in touch as soon as possible - this company is one of My Key Accounts, which means they take my advice on who to interview as we have a close working relationship. This means by applying through myself you may be in a new and exciting role faster than you think!I look forward to hearing from you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Altens  Staff]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob04BDF51977D6FF2A482579F5001C0241</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Altens-Staff_1664326.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My Client is looking for Mechanical Engineers in Aberdeen on a staff basis.The role is highly sought after and they already have interviews taking place.The role includes:- The specification, design and#38; documentation of Mechanical and#38; Hydraulic Systems, or individual components.  - The specification, selection and#38; procurement of Materials and#38; Services- To provide material costing information for project quotes and#38; able to assess the cost and#38; time implications of design decisions.  - The production, execution and#38; analysis of Test specifications- To author Operations Manuals, Maintenance procedures and#38; other Technical documents.  - The application of Industry standards to all engineering and#38; project activities undertaken- To liaise with Clients, suppliers and#38; peers during normal day-to-day activities.  - To carry out offshore surveys, installation, commissioning and#38; faultfinding services.  - To oversee Junior Engineers and#38; Technicians during design, manufacturing and#38; testing activitiesIf you are looking to change roles and grow your own career with an expanding and exciting Oil and Gas company, get in touch as soon as possible!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Subsea  Aberdeen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob51A132AF8CB42118482579F5001C0263</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Subsea-Aberdeen_1664327.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am looking for enthusiastic Mechanical Design Engineers for a Staff role with a well known Subsea Company in Aberdeen As Soon As Possible!My client has a couple of vacancies open to join their expanding and successful team to help take them to the next level in terms of projects and revenue in the Industry.They are a Global company with a view to doubling their turnover within the year - an exciting opportunity for any Mechanical Design Engineer with Subsea Experience!Skills Necessary:- 2+ Years in Subsea Oil and Gas- North Sea Experience- 3D Modelling and Design- Hand Calculations - TIER 1 VISADesirable:- Hydraulics Experience- HND CertificateIf you are looking for a new step in your career please get in touch as soon as you can - this is a candidate driven market, so only YOU have the power to change your situation for the better!I look forward to hearing from you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Account Manager Production Chemistry  Aberdeen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF31D530DE039361E482579F5001C0270</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Account-Manager-Production-Chemistry-Aberdeen_1664328.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a company who specialise in chemical engineering services to the oil and gas industry who are looking for an account manager to be based in Aberdeen. The account manager will be assigned a specific operator account and will be expected to ensure that service levels are kept high as well as identifying opportunities to develop business further. Key Requirements:-Experience from the oil and gas industry-Demonstrable sales track record-Chemical engineering or related degree. -Ability to demonstrate commercial awareness-Excellent interpersonal skillsThe role offers an excellent opportunity to develop commercial skills and to progress within a growing organisation. For more information please contact Thom Partridge at Huxley Associates.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Kintore  Subsea]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB3DC530CA7251D3F482579F5001C027C</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Kintore-Subsea_1664329.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I have an urgent requirement for a Design Engineer in the Kintore area of Aberdeen on a Staff basis to work with Subsea components. My client is looking for Mechanical Design Engineers to join them to be able to get their projects on track for the year due to their extensive expansion plans and their capacity for growth in the coming months. Requirements for this role include: - HNC Mechanical Engineering (or similar) - Mechanical Design Background - Ideally 2+ years in the Oil and Gas Industry - Hydraulics/Subsea/Materials Selection - Hand Calculations/FEA Ansys If you are interested in this role and would like to learn more about it, please get in touch as soon as possible. I would like to put a shortlist together by tomorrow morning of candidates who are available and suitable for the role, so please respond with an up to date CV and your suitability to the above requirements. If you are not looking for a move please refer someone to me who is, as I am able to reward you under our Huxley Associates referral scheme! I look forward to hearing from you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Engineer C C# Very competative package]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAD157420EEE7F24C482579F5001C028C</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Engineer-C-C-SHARP-Very-competative-package_1664330.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[OPPORTUNITY FOR A SOFTWARE ENGINEER TO JOIN A COMPANY WHO WILL SIGNIFICANTLY INVEST IN THE RIGHT CANDIDATE.GOOD MONEY, GREAT TRAINING AND A UNIQUE OPPORTUNITYMy client is currently looking for a Software Engineer to join their team in Aberdeen. This company is a large service companY who are involved in different sectors of the Oil and Gas industry. They are a great believer in organic growth, therefore they heavily invest in training and they have very detailed progression plans in place for a company orientated individual. The Roleand#149;Provide technical support to the offshore Marine and Process Control division and#149;Carry out Installation, Commissioning and upgrades of products and#149;Conducts surveys of Installations in support of sales/ projectsand#149;Report problems and improvements back to product responsible departments and or product support coordinator via appropriate QMS procedures The Personand#149;Education in Electronics, computer science or applied science and#149;3 years experience hands on experience of electronics in the field or base and#149;Valid offshore survival certificateThis is an exciting opportunity that will have a lot of response. To secure an interview please send me an updated CV ASAP. Once I have received your CV I will give you a call to discuss the position in more detail. Unfortunately there is no funding available for visa sponsorship.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project lead engineer StaffAberdeen Subsea Design focused]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB1CCADA89E16130A482579F5001C029A</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-lead-engineer-Staff-Aberdeen-Subsea-Design-focused_1664331.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A well established Subsea service company based in Aberdeen is looking to bring on board a project lead engineer on a staff basis.They require someone to come and work on their international projects while supervising/managing other members of the team.You will be required to work on a number of projects and you will need to be able to demonstrate you have the skills in project processes and design processes.Day to day role:-Deliver equipment with compliance to specification-Control product design for projects (including design review/approval)-Raise ECR-Review of projects-Managing design engineers and senior design engineersExperience:-oil and gas experience-previous design experience-projects experience-basic supervisory experience-proven practical engineering experience-experience executing projectsSalary: open at the momentIf you are interested in this role please can you send me your up to date CV today and I look forward to discussing this with you.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mechanical Design Engineer  Aberdeen  Staff]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD0D3A7A35954E6AA482579F5001C02A7</referencenumber>
<City><![CDATA[Aberdeen]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mechanical-Design-Engineer-Aberdeen-Staff_1669837.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is a large Subsea Service and Rentals company looking for a Mechanical Engineer to help them with their projects for the up and coming year.Their recruitment drive this year has proved successful so far and they are looking for this Engineer to help take their Operations Department to a new level.The Role involves:and#149;Experience: Relevant engineering and#149;Qualifications: Relevant Degree, HND or engineering experienceand#149;Subsea or Downhole experienceand#149;Landing String / Xmas Tree Knowledge preferableand#149;Design ExperienceoCarry out detail calculations (Pressure Vessel etc) to prove integrity of componentsoCreate / Review technical documentation and#150; Design specifications, Reports, Test ProceduresoRoot Cause AnalysisoDesign for ManufactureoKnowledge of engineering standards (API 6A, API 14A, ISO 13628-7) and practicesoCompetent in reviewing 2D and#38; 3D drawings for manufactureand#149;Engineering Database knowledge preferableand#149;Able to use AutoCad, Inventor and MathCadand#149;Computer LiterateIf you are looking for a new role in Mechanical Engineering please get in touch as soon as possible.With a One Stage Interview Process in place, you could be working for a company with a competitve salary and great benefits package next week!I look forward to hearing from you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Energy &amp; Utilities</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Refining Analyst, London £competitive]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob96A38E0C9B41AB18482579F5001C02EC</referencenumber>
<City><![CDATA[London]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Refining-Analyst-London-and-amp-SHARP163competitive_1639595.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[As a senior Analyst working within the downstream research team of a leading Energy Consultancy you will focus on the refining and refined product markets in the EMEA region. To a lesser extent your analytics will allow you to cover various other areas of the globe including Asia and the US and you will be required to provide support to the firms analysts all over the world.Main responsibilities include but not limited to:-Supply analysis of the EMEA-Forecasting product supply at both regional and country levels-Analysis of future oil supply and demand balances and implications for the refining industryThe successful applicant should have a good in depth knowledge of the refining business gained from previous work experience as well as a strong understanding of the refined products markets. Further to this a strong analytical mindset is important.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Trade Control Analyst Global Commodity Trading House]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob467A6B983E43E9F1482579F5001C02F9</referencenumber>
<City><![CDATA[London]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Principal-Trade-Control-Analyst-Global-Commodity-Trading-House_1639596.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is a market leading Commodity Trading House whoand#146;s growth and success has lead to the need to hire a senior Trade Control Analyst to strengthen this growing team. In this Front Office facing role, you will demonstrate your command of commodity trading strategy, and Product Control, analysing and defining trading limits for both London and overseas trading operations. You be responsible for the production of the daily Pand#38;L for both the physical and spec commodity trading books. In this highly influential role you will provide analysis and reports to executive board members and help both management and trading drive performance. As my client continues to expand globally, they are in the process of implementing major accounting and trading systems giving you the opportunity to be involved in the shaping and defining of the business as this pivotal time.    Candidate Profile: -Experience working in a physical commodity trading environment-Minimum of 3 years product control experience -Must be a Qualified Accountant-System implementation experience -Softs/Ags product experience beneficial-Numerate Degree level education -Confident communicator This is a rare opportunity to join a market leading Commodity Trading House. Simply send in your CV to register your interest in this fantastic opportunity or call Matt Cvijan on 0207 469 5055]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior reservoir engineer for service, Company]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0C75809C6B291077482579F5001C030A</referencenumber>
<City><![CDATA[Dubai]]></City>
<Country><![CDATA[UAE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Senior-reservoir-engineer-for-service-Company_1639597.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[The role of the reservoir engineer will entail:A Senior Reservoir Engineer will have considerable experience and may be recognised as a peer expert internally. Capable of independent work and management of reservoir engineering projects. Good problem-solving skills, an ability to solve unusual problems and able to tap into expert resources across the organisation. Competence in the key reservoir engineering skill areas with capability in one or more specialist skill areas.  The candidate should have experience in:A degree in engineering or a relevant science discipline, such as geology, physics, chemistry or mathematicsCompetent or skilled in key areas of reservoir engineering:Reservoir characterisationOil well performanceGas well performanceWater influxHydrocarbon recovery mechanismsReservoir simulationField appraisal,Field development planningSecondary and tertiary recoveryFluid characterisationWell test analysisCarbonate reservoir engineeringCarbon capture and storageField developmentAble to mentor and coach less-experienced Reservoir EngineersThe ideal Candidate should speak ArabicYou should be a wizard at Eclipse and Petrel softwareIf you feel you  match the criteria please reply with a updated cv, or if you know of anyone who may fit the profile please free to pass on these details to anyone in your network.(Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[COUNTRY HSE ADVISOR (Onshore  Kurdistan)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAD15F344F2FE4274482579F5001C0318</referencenumber>
<City><![CDATA[Iraq]]></City>
<Country><![CDATA[MIDDLE EAST]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/COUNTRY-HSE-ADVISOR-Onshore-Kurdistan_1639598.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[LOCATION:Erbil, Kurdistan. Residential role. No rotation.PACKAGE:NegotiableOVERVIEW:Lead HSSE professional with international Eand#38;P experience required to work and live in Kurdistan.No rotation possible.ESSENTIAL REQUIREMENTS:-10-15yrs Oil and Gas Eand#38;P Sector.-5 years in HSE at Superintendent or senior level.-Onshore Rigs experience-Experience in implementation and management of HSE-MS-Similar position held before with/in a major Oil and#38; Gas Operator.-Strong H2S risk management experience-A minimum of a Diploma in Safety Management (NEBOSH, OSHA, NIOSH, NOSA, etc, or other international recognized QHSE qualifications)ROLE:-Provide required support to Country operations management team in all HSE matters-Liaise with relevant officials and representatives from Country authorities on all HSE mattersPrevention-Verify compliance with Regulatory Requirements and Company requirements-Carry out periodic inspections of, and prepare inspection reports for, Company equipment (including safety equipment)-Promote operational practice which safeguard the environment and ensure that measures, procedures and#38; facilities are in place to address an environmental incident should it occur.(Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[PROJECT CONTROL DIRECTOR]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1773CA351429C2CD482579F5001C0327</referencenumber>
<City><![CDATA[Saudi Arabia]]></City>
<Country><![CDATA[MIDDLE EAST]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/PROJECT-CONTROL-DIRECTOR_1639599.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[LOCATION: Dammam, Saudi ArabiaPACKAGE: NegotiableOVERVIEW: Project Controls Director reporting to the VP required to have extensive petrochemical/oil and#38; Gas plant experience. Overseeing PCMs on many projects in Eastern Province of Saudi and Yanbu.ESSENTIAL REQUIREMENTS:-Degree in Engineering discipline-At least 20yrs experience in Project Control of projects-Proficient man manager-Worked for a major petrochemical company-Previous Middle East experience-Must be familiar to all the phases of projects including technical plans, design, Procurement, technical studies, specifications, Manpower management, testing, and evaluate changes as called -Licensed Engineer-Fluent in English language-Proficient in Microsoft Excel, Primavera, Window Based PC packages and application. DESIRABLE:PMI CertificationFluency in Arabic would be an asset.ROLE:Directs, plan and organize the overall Project Control Management. Proactively manage project progress, sub-contractors, procurement, analyzing project schedules / Budget Deviations, investigates causes, plan and implements corrective actions where necessary. Manage multiple phases of project including but not limited to project initiation, planning and scheduling, Cost engineering, estimating and quality surveying.(Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[OCTG SALES SPECIALIST]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFC1581814AD02BB9482579F5001C0336</referencenumber>
<City><![CDATA[Dubai]]></City>
<Country><![CDATA[UAE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/OCTG-SALES-SPECIALIST_1639600.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[LOCATIONDubai, UAEPACKAGE:Negotiable1 year fixed term - will be ongoing.OVERVIEW:Oil Country Tubular Goods specialist who has ideally worked for a Japanese trading or steel products company required.Should have at least 10yrs experience in the field.ESSENTIAL REQUIREMENTS:OCTG knowledgeHave worked for an OCTG trading company or manufacturing company.Should have a technical background then moved onto sales. 10yrs experience of OCTG required.DESIRABLE:Degree qualifiedWorked in the UAEROLE:New position within the company to increase trade of OCTG steel pipes within the Middle East.Knowledge of the Middle East oil companies would be advantageous.Yearly contracts will be renewed.(Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Engineering manager EPC]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1983257D9D2FC829482579F5001C0341</referencenumber>
<City><![CDATA[Dubai]]></City>
<Country><![CDATA[UAE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Engineering-manager-EPC_1639601.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[My client is a EPC company in Saudi Arabia, they are looking for a Engineering manager with a minimum of 8 years experince.(8 years minimum as a engineering manager) job summary: Manages in directing. coordinating and exercising functional engineering authority for planning, organisation, control, Integration and completion of the project within area of assigned responsibility. Primary duties: Managing engineering staff Manages the implementation of project plans previously determined and agreed upon based om the specified time frame, funding limitations, procedures of accomplishing, staffing requirements.Closely coordinate activities of engineering crews to ensure project progress on schedule and within prescribed budProvide technical advice and to resolve problems. Comply with all safety regulations and procedures, Attend training courses seminars etc required by the company. Work Experience at least 8 to 10 years work experience as a engineering manager in oil, gas and petrochemical industries. Must be familiar with to specific phases of project, technical studies,designs, specifications, technical plans, testing and evaluate charges as called for. Middle east experience is an advantage. Education Masters/Bachelors Degree,diploma in Any engineering courses If you feel you match the criteria above please send me a updated version of your cv, or if you know of anyone who maybe interested please feel free to pass this on. (Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Emirati Accountant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF51482AB0195B5CD482579F5001C034E</referencenumber>
<City><![CDATA[Dubai]]></City>
<Country><![CDATA[UAE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.miningjob.net/job/Emirati-Accountant_1639602.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[The role of a financial accountant is to carry outa review of, evaluate and conclude on, financial information of the vendors/contractors application for pre-qualification and registratiom as laid dow in the group procedures for determining their financial capability for execution of projects/supply of materialsJob dimensions: number of contractors/vendors applications expected to be reviewed over the next one year 200 to 300Daily taske will include the below:Receive and log applications for contract /vendor prequalification and registrationEvaluate all financial information provided including the audited finacial statementsConclude on the evaluation to determine the financial capabilities of the applicants, also recommending, if prequalified, the extent of the value that can be awarded, taking into account various factors including existing contracts, and other aspects that may be evident from the annual /financial reportCoordinate/communicate with contracts and purchasing department.track all prequalification carried out, maintain record of evaluations, prepare weekly reportsCandidate skills and experience should have the below:You should be a graduate with a degree in economics or accountancy.Good working knowledge of computer system and accounting software and MS office programsAt least 5 years experience in Finance or in the area of financial economic analysis.If you feel you match the above criteria please send a updated version of your cv.(Huxley Associates Global Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Market Risk Data and Trade Control Analyst]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D4E17F729F9D9F3482579F5001C047E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Market-Risk-Data-and-Trade-Control-Analyst_1669838.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[BIG 6 Energy Major seeks Market Risk Analyst - London 30k  My Client is a leading BIG 6 Energy Major whos continued success has created a vacancy for a Market Risk Analyst to strengthen their growing Energy Market Risk Team. This is an entry point into Energy Risk reporting at one of the most respected companies in the industry. You will be responsible for producing and reviewing risk analysis, ensuring the integrity of the risk data. In this high visibility role you will independently review the forward curve making sure that it is market reflective. You will join a highly skilled team of risk specialists leading the implementation of risk indicators and controls within the business.  The following skills are required:  - Minimum 12-18months experience within the Energy Sector - Strong IT skills- VBA modelling ability - Good report writing ability  - Numerate Degree level education 2:1 or above  This is a fantastic opportunity for you to establish yourself as an Energy Risk professional with clear career progression within the business into Strategic positions and the potentially Front Office. The Salary is competitive and is coupled with an excellent bonus and benefits package. Submit your CV to register your interest.   To find out more about Huxley Associates please visit  www.huxley.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Mining &amp; Extraction</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Productie leider, Venlo]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5D2484C8F55B70A0482579F5001C048A</referencenumber>
<City><![CDATA[Limburg]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Productie-leider-Venlo_1639626.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A FMCG company is currently looking for a Production Leader for their production site in the area of Venlo. The Production Leader is responsible for production planning and coaching of the shift leaders and planners on the production site. Furthermore he/she is expected to initiate and lead improvement programs according to TPM within the department and production. Requirements: and#149;Bachelor Degree (HBO diploma)and#149;Production planning experienceand#149;Management experienceand#149;Excellent communication skills in English and Dutch Interested candidates send their profile to Monique Dressel at Huxley Associates. 020 522 1333 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[S&OP Planner FMCG]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE9280254C0460844482579F5001C0499</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/S-and-amp-SHARP38OP-Planner-FMCG_1639627.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A FMCG company in Noord-Brabant is currently looking for a Sand#38;OP planner. The Sand#38;OP planner is responsible for the sales and operational planning processes with respect to demand planning, preparation of production planning and sales targets. He/she works closely with sales and#38; marketing, finance, customer service and logistics. Further responsibilities include the planning of supply chain and Sand#38;OP processes for new product introductions what includes contact with Rand#38;D. Externally the planner will have contact with suppliers and customers. The role of the planner focuses on forecast accuracy, product availability, stock level control and optimisation and efficient new product to market processes.  The ideal candidate for this position has a Bachelor Degree and about three to six years of experience in a planning position within supply chain mainly covering forecasting and demand planning. Experience in an international FMCG environment is an advantage. Excellent communication skills in English are a must. Language skills in Dutch, Spanish or Portuguese are an advantage. Interested candidates end their profile to Monique Dressel at Huxley Associates. 020 522 1333and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Productie leider, Venlo]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF87B7AF4BD9FCCBE482579F5001C04A5</referencenumber>
<City><![CDATA[Limburg]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Productie-leider-Venlo_1639628.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A FMCG company is currently looking for a Production Leader for their production site in the area of Venlo. The Production Leader is responsible for production planning and coaching of the shift leaders and planners on the production site. Furthermore he/she is expected to initiate and lead improvement programs according to TPM within the department and production. Requirements: and#149;Bachelor Degree (HBO diploma)and#149;Production planning experienceand#149;Management experienceand#149;Excellent communication skills in English and Dutch Interested candidates send their profile to Monique Dressel at Huxley Associates. 020 522 1333 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SUPPLY CHAIN PLANNING MANAGER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob792E87CD993C09AE482579F5001C04B4</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SUPPLY-CHAIN-PLANNING-MANAGER_1639629.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een sterk groeiende innovatieve cliand#235;nt van formaat zijn wij per direct op zoek naar een SUPPLY CHAIN PLANNING MANAGER. De werkzaamheden in functie zijn o.a. : In deze nieuwe rol krijg je de volledige vrijheid om de SUPPLY CHAIN PLANNING AFDELING IN TE RICHTEN. Je stuurt een team van 2 planners aan en een grondstoffenbeheerder. Je organiseert en stuurt de operationele productieplanning, inkoopplanning aan. Je bewaakt onder andere de voorraadwaardes en leveranciersperformance. Daarnaast geef je actief leiding aan projecten. Je bent proactief, zelfstandig en hebt de juiste inhoudelijke kennis. Je hebt oog voor optimalisatie. Je rapporteert aan de SUPPLY CHAIN MANAGER. Deze rol kan bij succes jouw volgende stap betekenen. Je staat open voor verandering! Je wil groeien en jezelf bewijzen in deze kansrijke omgeving met doorgroeimogelijkheden!  Profiel: - Minimaal afgeronde HBO/WO opleiding of gelijkwaardig door ervaring - Een achtergrond in een productie/logistiek in FMCG/FOOD omgeving - Nuchter - Verantwoordelijkheid - Je bent zelfstandig - Kennis van Exact . Geboden wordt: Zakelijke, informele, plezierige werkomgeving met korte lijnen, waar genoeg ruimte is om je verder te ontwikkelen en je persoonlijke ambities te realiseren. Geand#239;nteresseerd? Een veelbelovende carriand#232;re en een vaste positie bij een snel groeiende organisatie! Stuur je CV in word.doc naar de link. Ben je geand#239;nteresseerd in een nieuwe uitdaging op een van deze gebieden en heb je een gedegen achtergrond in FOOD maar sluit de bovenstaande functie niet volledig bij je profiel aan, stuur dan ook je c.v. in word.doc naar de link. Huxley Associates: If not now, when? and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Demand Planner (S&OP), Den Bosch, 36K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE292806095DDFE0D482579F5001C04C7</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Demand-Planner-S-and-amp-SHARP38OP-Den-Bosch-36K_1639630.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[For a state of the art multinational we are searching for strong Demand specialists As a Demand Planner you are responsible for e.g. Demand planning and Sales target definition (Sand#38;OP). secure and deliver independent requirements which are forecasted by the demand planning department. You coordinate together with corporate and internal departments in order to create short and mid term plans. You focus on maintaining safety stock levels You will participate in cross functional project groups Profile Bachelor/masters degree with a minimum of 2 years experience Experience with Sand#38;OP Experience with SAP, Manugistics Languages, flawless in English written and#38; verbal FMCG experience is preferable Region Den Bosch  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sourcing Manager Vacancy  Gloucestershire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0900665C046BA92F482579F5001C04D2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sourcing-Manager-Vacancy-Gloucestershire_1639631.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Sourcing Manager Vacancy - GloucestershireKey responsibilities include:Analysing the supply chain to identify risks and opportunities Negotiate and manage contracts and to achieve the best price. Manage suppliers through agreed SLAs. Lead cost reduction activies and look to take cost out of all stages of the supply process. Liase with key business stakeholders to ensure business and supply chain goals are aligned. and#160;Requirements:Experience in strategic sourcing environment. Proven knowledge of purchasing strategy. Experience within an Engineering environmentAbility to work proactively with minimum supervisionAbility to set and meet own objectivesand#160;and deadlinesApply now for immediate consideration.Location: GloucestershireDuration: PermanentSalary: and#163;35,000 - and#163;40,000 + benefits]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior BuyerLeicestershirecirca £35,000£45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6CCC69E2FAA4B035482579F5001C04E1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Buyer-Leicestershire-circa-and-amp-SHARP16335000-and-amp-SHARP16345000_1639632.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client, a leading UK manufacturer based in the East Midlands currently requires a senior buyer. This is an excellent opportunity to take a step up in your career as this role will give you the opportunity for progression internally also.  Due to changes in the market and industry sector Procurement has now become a much more vital division within this business. My client is seeking a buyer with a strong strategic and project driven background ideally in a manufacturing environment. Whilst you will not have man management responsibility this is your chance to become a real leader in the team. To be successful in this role you will have worked in a fast paced manufacturing environment. Due to the nature of their business you will work closely with other divisions in the business including design. Ideally experience in electronics or lighting is desirable. This is a fast paced environment where the possibility of change is highly likely.  You must be adaptable to change but also have the ability to properly manage these changes effectively. To be considered for this role I will need an updated copy of your CV. Please note that shortlisting will be taking place throughout the week. Unfortunately feedback cannot be provided due the volume of applications received.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Category Buyer  Strategic Procurement  Wiltshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1B0B101761BFE235482579F5001C04ED</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Category-Buyer-Strategic-Procurement-Wiltshire_1639634.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Category Buyer - Strategic Procurement - WiltshireYour role as Category Buyer will include sourcing and selecting suppliers, developing, coordinating and implementing procurement strategies, negotiating terms, monitor KPIs and managing supplier arrangements and service level agreements.  This will be a strategic role so we are not just looking for someone that processes orders but looks to take cost out of the supply chain at all stages and maintain the reliability of supply within your categories on a national level.It is expected you will have a proven track record in a procurement environment to ensure the supply chain is robust, reliable and offers significant financial benefits to the organisation as a whole.  You will manage a category spend of over and#163;50m and manage contracts on a national basis so this will be a great role for an ambitious candidate who is looking to progress their career. Ideally you will hold or be working towards the MCIPS certification. For immediate consideration please apply NOW and I will call you to run through the role. Salary: and#163;33,000 - and#163;35,000 +benefitsDuration: PermanentLocation: Wiltshire]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Category Buyer  Strategic Procurment  Wiltshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob101949ED709A4C42482579F5001C04FA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Category-Buyer-Strategic-Procurment-Wiltshire_1639635.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Category Buyer - Procurement - WiltshireHuxley Associates are working with a leading organisation based in Wiltshire to recruit a Procurement Category Buyer to join their team.  This will be an opportunity to work for a leading organisation where you can take on a high level of responsibility from the start.  Your role will include supplier management, strategic sourcing, developing and implementing procurement strategies, contract negotiation, develop and monitor KPIs, work with key internal stakeholders to manage the needs of the business and rationalisation of the supplier base to realise cost savings and improvements in supplier relationships.To be considered we want to see you have a proven procurement background and want to continue to progress your career in this field.  Any experience of purchasing for Commercial Fleets would be highly beneficial as would CIPS certification.For immediate consideration please apply NOW. Salary - and#163;33,000 - and#163;35,000 Duration: PermanentLocation: Wiltshire]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Demand Planner (S&OP), Den Bosch, 36K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCFADB425B8A50626482579F5001C0504</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Demand-Planner-S-and-amp-SHARP38OP-Den-Bosch-36K_1639636.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[For a state of the art multinational we are searching for strong Demand specialists As a Demand Planner you are responsible for e.g. Demand planning and Sales target definition (Sand#38;OP). secure and deliver independent requirements which are forecasted by the demand planning department. You coordinate together with corporate and internal departments in order to create short and mid term plans. You focus on maintaining safety stock levels You will participate in cross functional project groups Profile Bachelor/masters degree with a minimum of 2 years experience Experience with Sand#38;OP Experience with SAP, Manugistics Languages, flawless in English written and#38; verbal FMCG experience is preferable Region Den Bosch  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Productie leider, Venlo]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7658B83B5DA1D028482579F5001C0510</referencenumber>
<City><![CDATA[Limburg]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Productie-leider-Venlo_1639637.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A FMCG company is currently looking for a Production Leader for their production site in the area of Venlo. The Production Leader is responsible for production planning and coaching of the shift leaders and planners on the production site. Furthermore he/she is expected to initiate and lead improvement programs according to TPM within the department and production. Requirements: and#149;Bachelor Degree (HBO diploma)and#149;Production planning experienceand#149;Management experienceand#149;Excellent communication skills in English and Dutch Interested candidates send their profile to Monique Dressel at Huxley Associates. 020 522 1333 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Purchasing Manager  Bristol  Manufacturing]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob32484CC17F32089D482579F5001C051B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Purchasing-Manager-Bristol-Manufacturing_1639638.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Purchasing Manager - Bristol - ManufacturingHuxley Associates are working with a multinational manufacturing / engineering company based in Bristol to help them find a Sourcing Manager / Purchasing Manager to join their team. This will be a varied and challenging role including defining the purchasing strategy, leading negotiations and formulating contracts with suppliers, identify opportunities and risks in the supply chain. Finally key to this role will be the ability to influence stakeholder both internally and externally. As the ideal candidate you will have a successful career history to date in a purchasing / supply chain / strategic sourcing role in a manufacturing or engineering environment. Ideally you will be working towards MCIPS or have a business management degree. Salary: and#163;35,000 - and#163;40,000 + bens Duration: Permanent Location: Bristol. For immediate consideration and interview this week please reply now with your updated CV and contact details and I will call you to run through the role.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Category Buyer  Procurement  Wiltshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob53D143215E5A70CA482579F5001C052B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Category-Buyer-Procurement-Wiltshire_1639639.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Category Buyer - Procurement - WiltshireHuxley Associates are working with a leading organisation based in Wiltshire to recruit a Procurement Category Buyer to join their team.  This will be an opportunity to work for a leading organisation where you can take on a high level of responsibility from the start.  Your role will include supplier management, strategic sourcing, developing and implementing procurement strategies, contract negotiation, develop and monitor KPIs, work with key internal stakeholders to manage the needs of the business and rationalisation of the supplier base to realise cost savings and improvements in supplier relationships.To be considered we want to see you have a proven procurement background and want to continue to progress your career in this field.  Any experience of purchasing for Commercial Fleets would be highly beneficial as would CIPS certification.For immediate consideration please apply NOW. Salary - and#163;33,000 - and#163;35,000 Duration: PermanentLocation: Wiltshire]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HBO starter position in production planning]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob02F65B1F7CEAFEAF482579F5001C0537</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/HBO-starter-position-in-production-planning_1639640.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[A food company in the area of Amsterdam is looking for a production planner. The position is excellent for someone who wants to learn everything about production planning in a fast-paced and challenging environment that has to ensure the production and delivery of a diversity of products on a daily basis. The production planner is part of the planning team that is responsible for the daily planning of production according to daily forecasts. The ideal candidate for this position matches the following requirements:and#149;Bachelor degree / HBO diploma and#149;Production planning experience (internship, stage, part-time job, first job) and#149;Excellent communication skill in English and Dutch Interested candidates send their profile to Monique Dressel at Huxley Associates. 020 522 1333 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Junior Productieplanner  32k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob11B2B19B337C5062482579F5001C0546</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Junior-Productieplanner-and-amp-SHARP150-32k_1639641.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Heb je een HBO Logistiek opleiding? Heb je ervaring in productie planning van ongeveer 2 jaar en ben je op zoek naar een uitdagende productie planning functie in een fast-paced omgeving? Een voedingsmiddelbedrijf in de regio Amsterdam zoekt jouw voor een productieplanner functie. In deze functie ben je onderdeel van een planningsteam dat dagelijks de planning voor doorgaande productie verzorgt. Er zijn tien verschillende ploegen en een veeltal aan producten welke dagelijks geproduceerd en geleverd moeten worden. Dit maakt deze functie uitdagend en veelzijdig. Functie eisen:and#149;HBO opleiding bij voorkeur in de logistiekand#149;Twee jaar ervaring in een productie planning functieand#149;Uitstekende communicatieve vaardigheiden in Engels en Nederlands Heb je interesse in deze functie? Stuur je CV dan tav Monique Dressel naar Huxley Associates. 020 522 1333 and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Customs Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3E0927C189B2292A482579F5001C0551</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Customs-Specialist_1639642.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een grote logistieke dienstverlener ben ik op zoek naar een customs specialist voor de vestiging in de omgeving Amsterdam.and#60;band#62;Verantwoordelijkheden:and#60;/band#62;- opstellen van douaneaangiften en de volledige afhandeling hiervan;- signaleren van fiscale risicoand#146;s;- zorgdragen dat openstaande posten aan rechten en belastingen tijdig worden ingelost;- douanetechnische problemen signaleren en oplossingen aandragen;- up-to-date houden van vaktechniek binnen de douane- en belastingwetgeving. and#60;band#62;Functievereisten:and#60;/band#62;- MBO+ werk- en denkniveau;- afgerond diploma Declarant (bv. EVO/Fenex);- enkele jaren ervaring op een douaneafdeling;- stressbestendig, accuraat en probleemoplossend vermogen;- zowel zelfstandig als in teamverband kunnen werken;- goede beheersing van de Nederlandse en Engelse taal in woord en geschrift.Interesse? Reageer dan met een actueel CV via de onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Declarant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA47B0AC48D71B735482579F5001C055F</referencenumber>
<City><![CDATA[Zuid]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Declarant_1639643.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een grote internationale logistieke dienstverlener zijn wij op zoek naar een Declarant voor de vestiging in de omgeving Rotterdam.and#60;band#62;Functieomschrijvingand#60;/band#62;De dagelijkse werkzaamheden bestaan onder meer uit het volgende: - zelfstandig maken van de verschillende aangiftes;- opmaken van verschillende douanedocumenten;- behandelen van niet-communautaire goederen (zowel inkomende als uitgaande goederen);- behandelen en indienen van UTBand#146;s, COEand#146;s;- maken van diverse verzoeken richting douane (bv. bezwaar maken, buiten werking stellen, e.d.);- diverse lichte administratieve werkzaamheden (bv. het administratief afhandelen van export- en importdossiers, e.d.). and#60;band#62;Functie eisen:and#60;/band#62;- MBO/HBO werk- en denk niveau;- Declaranten diploma;- relevante en recente ervaring als declarant;- beheersing van de Engelse en Nederlandse taal;- ervaring met douane aangifteprogrammas;- accuraat, stressbestendig, flexibele werkhouding, zowel zelfstandig als in teamverband kunnen werken;- ervaring met MS Outlook, MS Excel, MS Word.Interesse? Reageer met een up-to-date CV via de onderstaande link.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Recruitment consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob09008D494815112F482579F5001C0577</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Recruitment-consultant_1639644.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates is looking for recruitment consultants!Visit our websites, www.huxley.be/ and www.sthreecareers.com to learn more about the company itself, as well as our culture and its vision for the future. If you have any questions, please feel free to contact me by either mail or phone.What is the job about? - Actively find clients and maintain relationship with existing ones- Writing adverts- Searching our well established database for candidates - Preparing both candidates and clients for interview - Negotiating with candidates and clients - Taking verbal references - Building rapport and trust with your clients and candidates What person are we looking for? First and foremost, we are looking for a strong individual, that can work independently. Important is: - Commitment- Self-motivation- Strong minded- Competitve attitude- Clear and confident manner- Minimum bi-lingual: English and Dutch/French What does SThree offer?- A growing international company- An extensive 18 months training program - A basic salary + uncapped commission- A meritocratic system- A company which rewards its consultantsHave you recognized yourself in this description? Please do send your cv to kaat.verlinden @ huxley.be or call me at 02/557.71.03Thank you in advance and have a great day!and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Demand planner]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE95765F2BEEA2CA2482579F5001C0581</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Demand-planner_1639645.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Hi everyone!I am looking for a demand planner in the region of Brussels. Are you looking for a new challenge, and do you have experience with: - forecasting, making demand forecast models- interacting with sales, marketing and customer finance to understand the main drivers behind demand- Providing input to the Supply Planning organization in developing inventory strategies on existing items, new products, and product phase-outsIf you had such experience before, and are interested in knowing more about the job. Please do send me your CV to the e-mail below, and give me a call soon after to discuss your qualifications. Thanks in advance and have a great day. Best regards,    Kaatje Verlinden Supply Chain DivisionHuxley Associates00 32 2 557 7103k.verlinden @ huxley.behttp://www.huxley.com  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Customer support]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob62EC656234346F4E482579F5001C058F</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Customer-support_1639646.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[For a key client, I am currently looking for a Customer Support Supervisor. Do you have experience in customer support - supply chain related? Can you lead and coach a team?Do you speak Dutch and English? If you answered yes to all the questions above - please do call me at 02/557.71.77 or e-mail your cv to k . verlinden @ huxley . beIs this not applicable to your own profile, but you know someone else with these requirements - please do not hesitate to share my contact details. Thanks in advance and have a great day.Kaatje VerlindenHuxley AssociatesSupply Chain Recruitment02/557.71.77k.verlinden @ Huxley. be and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Consultant WMS]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob39EFBADEE5448948482579F5001C059A</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Consultant-WMS_1639647.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[I am currently looking for a WMS applications consultant. Do you have experience in WMS? Are you project oriented? Are you prepared to work as a consultant and visit external clients? If you answered yes to the above questions and you are looking for a new challenge, please do contact me on the number below after sending me your cv. Do you think this advert is not applicable to your situation, please do send it to people in your network that might be interested. Thanks in advance and have a great day!Best regards,      Kaatje Verlinden Supply Chain DivisionHuxley Associates00 32 2 557 7103k.verlinden @ huxley.behttp://www.huxley.com  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Warehouse teamleader]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob49FB62342522927C482579F5001C05A5</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Warehouse-teamleader_1639648.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Hello everyone!For a key client I am looking for a junior warehouse teamleader. - Do you speak Dutch and French? - Do you have warehouse experience?- Do you adapt easily to new environments and are social towards others? - Are you willing to manage a team?- Do you have a hands-on mentality? - Are you willing to learn? If you answered yes to the above questions and you are looking for a new challenge, please do contact me on the number below after sending me your cv. Do you think this advert is not applicable to your situation, please do send it to people in your network that might be interested.  Thanks in advance and have a great day!Kaatje VerlindenHuxley AssociatesSupply Chain Recruitment02/557.71.77k.verlinden @ Huxley. beand#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Importexport Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob903D9CFC3D3A6284482579F5001C05B3</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Import-export-Specialist_1639649.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Hi Everyone!For a big international company I am looking for an import and export specialist. Please do get in touch with me if you have experience with: - import/export compliance concerning IATA, Incoterms, WTO rulings, VAT- import/export to coutries/regions such as: Japan, China, Russia, Switzerland, USA, EU and South America. Also important: Do you speak English? Can you work independently? Are you self-motivated? If you think your profile matches what I am looking for, please send me your cv and I will contact you soon after. Ill be looking forward to working with you in the future. Thanks in advance and have a great day!Kaatje VerlindenHuxley AssociatesSupply Chain Recruitment02/557.71.77k.verlinden @ Huxley. be and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Improvement Consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1DDB4985EE146EB5482579F5001C06ED</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Improvement-Consultant_1651623.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Excellent opportunity for experienced business consultants form big consultancy firms who are looking for a smaller but highly professional environment that offers them the opportunity of more freedom, influence and involvement. This is a highly interesting position for professionals who have gained experience as consultant with a specialisation in procurement, supply chain or change management in one of the major consultancies and are looking for a new challenge.  The consultant in this role is working in long-term projects with multinational clients in the food and pharmaceutical industry. The projects include the whole process form analysis to execution and concern mainly supply chain and procurement processes or business processes related to this (e.g. purchase-to-pay, logistic chain, communication processes, and#133;). This is an essential difference to other consultancies in which the task of the consultants ends where it actually gets interesting. In this role it is expected that the consultant is analysing the current situation, develops and designs an appropriate project plan to achieve the established common goal and is deeply involved in executing this pan in co-operation with relevant internal parties on the client side. The company is looking for Consultants with about five years of experience covering supply chain, procurement and business improvement projects at clients in the Netherlands. The consultancy experience was preferably gained in a major consultancy company ensuring that the consultant has experience in dealing with projects on strategic level with big impact at international companies or  multinationals. Excellent communication skills in English and Dutch are expected. Interested candidates send their profile to Monique Dressel at Huxley Associates. 020 522 1333and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[IT Buyer  IT  Comms Systems  Gloucestershire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3300EA4A3C19F8B5482579F5001C06FE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/IT-Buyer-IT-Comms-Systems-Gloucestershire_1651624.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are recruiting for an IT Buyer to join a successful organisation in the Gloucestershire area.  We are looking for someone who has worked in a purchasing role for IT software and Hardware systems.  They work with all the big names and partner with them to ensure they can deliver the best services across the market.  You will join their large purchasing team and take responsibility for a few category areas working with supplier to reduce costs and manage key relationships.To be considered you will have:- A few years experience in a buying / purchasing role. - Experience in purchasing IT Systems and comms- Strong skills in managing supplier relationships- Good negotiation skills For immediate consideration please reply NOW with your updated CVand#163;30,000 - and#163;35,000 + benefits.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[MCIPS Certified Purchasing Manager Required  Wiltshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0611F5A7684D7D14482579F5001C0709</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/MCIPS-Certified-Purchasing-Manager-Required-Wiltshire_1651625.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are searching for an MCIPS certified Purchasing Manager to work for a Blue-Chip organisation in the Wiltshire area. You will be responsible for a budget of over and#163;50m per annum with over 25 suppliers to manage across several direct and#38; indirect commodity areas. You will be responsible for creating and implementing the procurement strategy for those commodities and also the planning and#38; execution of cost savings projects related to them. Furthermore you will manage and develop strategic supplier relationships, utilising KPI targets for cost, delivery and#38; quality through holding regular review meetings, supplier audits and industry benchmarking. Location: WiltshireDuration: PermanentSalary: and#163;33,000 - and#163;35,000For immediate consideration please apply NOW.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement ManagerGlobal Business circa £60,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob08D5E7F3E98DAAB4482579F5001C0718</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager-Global-Business-circa-and-amp-SHARP16360000_1651626.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Do you want to working for a market leading manufacturing organisation? Have you had global exposure and responsibilities?The ideal candidate will currently be working in a global business, working with a huge multi million pound spend over a very small number of products. You will have good eye for contracts and understand legal implications. This is an excellent opportunity for a senior procurement professional with a strong and successful track record of strategic contract negotiation. This is a business critical role offering career progression in the future to Procurement Director.As much as 50% of your time will be spent travelling to areas such as Australia, Russia, Europe, the United States and#38; Asia. To apply you will need an up to date CV.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Consultant  Den Haag]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4B64BE20D163900A482579F5001C0727</referencenumber>
<City><![CDATA[Den Haag]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Consultant-Den-Haag_1658645.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een electronics organisatie in de omgeving van Den Haag ben ik op zoek naar een Supply Chain Consultant. In deze rol ben je als rechterhand van de Supply Chain manager verantwoordelijk voor de ontwikkeling van de lange termijn visie en strategie van het supply chain management. Je vertaald hierbij de strategie naar heldere afdelingsdoelstellingen en jaarplannen. Je adviseert diverse management lagen en bent in staat het MT en Executive Board te overtuigen van je bevindingen.Profiel:- WO opgeleid- 5 jaar soortgelijke werkervaring - Ruime ervaring in advisering en presenteren op senior management niveau- Kennis van en ervaring in project management- CPIM APICS is een pre- SAP kennis- Ervaring in verander- en verbetermanagementVoldoe je aan bovenstaand profiel en wil je graag meer informatie ontvangen? Klik op de link om je CV naar me toe te sturen.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Inkoper, Amersfoort, Consumer Goods]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA061C962FEB87072482579F5001C0735</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Inkoper-Amersfoort-Consumer-Goods_1664332.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een retailer in de omgeving van Amersfoort ben ik op zoek naar een Senior Inkoper (50-60k). Je bent verantwoordelijk voor het inkooppakket van een productgroep. Je bepaalt hiervoor de inkoopstrategie, zorgt voor een optimaal commercieel resultaatProfiel:- Je beschikt over een HBO/WO opleiding - Je hebt 3-5 jaar werkervaring in de inkoop- Je beschikt over een Nevi 1 / 2 certificaat- Je bent commercieel gedreven- Je hebt retail ervaringVoldoe je aan bovenstaand profiel en heb je interesse? Stuur je CV via de link naar me toe!  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QC Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8AB884E4132176E9482579F5001C0742</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QC-Manager_1664333.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Manager Quality ControlLevensmiddelen industrie (vers)Full-time 40 uur per weekVaste aanstelling (1 jaar contract start)Salaris tussen de and#128; 45.000,- en and#128; 60.000,- per jaar Rapporteren aan Technologie Manager.Functie- Verantwoordelijk voor het dagelijks aansturen van de operationele kwaliteitsafdeling op de werkvloer, bestaande uit 15 mensen, waarbij persoonlijke en professionele ontwikkeling hoog in het vaandel staat- Monitoren van de naleving van procedures, voorschriften en wetgeving op gebied van kwaliteit  en indien nodig het (laten) opleiden en trainen van operators- Sturing geven aan kwaliteitsverbeterprojecten, zowel op eigen initiatief als naar aanleiding van analyses door de Manager QA- Opvolgen van niet-conforme producten en initiand#235;ren van correctieve acties - Waarnemen van trends en ontwikkelingen binnen kwaliteitszorg in zijn algemeenheid en binnen de vleesindustrie in zijn bijzonder Profiel:- HBO niveau opleiding Levensmiddelentechnologie of vergelijkbaar- Relevante ervaring in een vergelijkbare functie binnen een food productieomgeving- Daadkrachtige people manager die mensen motiveert en betrokkenheid optimaliseert - In staat om binnen korte tijd een netwerk op te bouwen en zaken gedaan te krijgen, stelt de juiste prioriteiten- Flexibel ingesteld en vindt het een uitdaging om een spilfunctie te vervullen, wordt gezien als autoriteit- Persoonskenmerken: analytisch, resultaatgericht, hoog probleemoplossend vermogen, stressbestendig, overtuigend, ambitieus, proactief en communicatief sterk.Een uitgebreid functieprofiel is beschikbaar wanneer we je CV in word.doc hebben ontvangen.Wil je meer informatie over deze en/of andere posities, neem dan direct contact op met Jan-Willem Broekhoven via nummer 020-5221333 en stuur je CV via de link op deze pagina.Huxley Associates Food is gespecialiseerd binnen de verschillende niches in de voedingsmiddelen industrie. - Productie/operationeel,- Planning,- Inkoop,- Sales and#38; Marketing,- QA/QC (HSE),- Rand#38;D/procestechnologie,- Maintenance.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QC Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob80ED1F338FA88EFC482579F5001C074F</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QC-Manager_1664334.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Manager Quality ControlLevensmiddelen industrie (vers)Full-time 40 uur per weekVaste aanstelling (1 jaar contract start)Salaris tussen de and#128; 45.000,- en and#128; 60.000,- per jaar Rapporteren aan Technologie Manager.Functie- Verantwoordelijk voor het dagelijks aansturen van de operationele kwaliteitsafdeling op de werkvloer, bestaande uit 15 mensen, waarbij persoonlijke en professionele ontwikkeling hoog in het vaandel staat- Monitoren van de naleving van procedures, voorschriften en wetgeving op gebied van kwaliteit  en indien nodig het (laten) opleiden en trainen van operators- Sturing geven aan kwaliteitsverbeterprojecten, zowel op eigen initiatief als naar aanleiding van analyses door de Manager QA- Opvolgen van niet-conforme producten en initiand#235;ren van correctieve acties - Waarnemen van trends en ontwikkelingen binnen kwaliteitszorg in zijn algemeenheid en binnen de vleesindustrie in zijn bijzonder- Intensief samenwerken met de Manager QA en de Manager Operations Profiel:- HBO niveau opleiding Levensmiddelentechnologie of vergelijkbaar- Relevante ervaring in een vergelijkbare functie binnen een food productieomgeving- Daadkrachtige people manager die mensen motiveert en betrokkenheid optimaliseert - In staat om binnen korte tijd een netwerk op te bouwen en zaken gedaan te krijgen, stelt de juiste prioriteiten- Flexibel ingesteld en vindt het een uitdaging om een spilfunctie te vervullen, wordt gezien als autoriteit- Persoonskenmerken: analytisch, resultaatgericht, hoog probleemoplossend vermogen, stressbestendig, overtuigend, ambitieus, proactief en communicatief sterk.Een uitgebreid functieprofiel is beschikbaar wanneer we je CV in word.doc hebben ontvangen.Wil je meer informatie over deze en/of andere posities, neem dan direct contact op met Jan-Willem Broekhoven via nummer 020-5221333 en stuur je CV via de link op deze pagina.Huxley Associates Food is gespecialiseerd binnen de verschillende niches in de voedingsmiddelen industrie. - Productie/operationeel,- Planning,- Inkoop,- Sales and#38; Marketing,- QA/QC (HSE),- Rand#38;D/procestechnologie,- Maintenance.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QA Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob97317DAC1FB2B3E1482579F5001C075E</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QA-Manager_1664335.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Manager Quality AssuranceLevensmiddelen industrie (vers)Full-time 40 uur per weekVaste aanstelling (1 jaar contract start)Salaris tussen de and#128; 45.000,- en and#128; 60.000,- per jaar Rapporteren aan Technologie Manager.Functie - Verantwoordelijk voor het beheren en verbeteren van kwaliteitssystemen- Verzorgen van periodieke rapportages aangaande zaken als kwaliteitssysteem, audits en klachtenafhandeling en dit vertalen naar verbetervoorstellen- Bijhouden en analyseren van actuele trends en toekomstige wijzigingen op het gebied van wet- en regelgeving en vertalen van de ontwikkelingen naar de organisatie- Voorbereiden, begeleiden en uit (laten) voeren van interne en externe audits.- Onderhouden van contact met klanten, leveranciers en audit- en controleorganisaties - Intensief samenwerken met Manager QC en de Manager Operations  Profiel - HBO/ Academisch werk- en denkniveau, bij voorkeur een opleiding Levensmiddelentechnologie of vergelijkbaar- Relevante werkervaring op QA gebied binnen een food productieomgeving - Gedegen kennis van actuele kwaliteitssystemen (HACCP, BRC)- Is flexibel ingesteld en vindt het een uitdaging om te werken binnen een dynamische groeiende onderneming- Bouwt een solide netwerk met zowel klanten als collegaand#146;s van verschillende afdelingen- Persoonskenmerken: analytisch vermogen, communicatief vaardig, stressbestendig, resultaatgericht, nauwkeurig, zelfstandig, ambitieus, leergierig.Een uitgebreid functieprofiel is beschikbaar wanneer we je CV in word.doc hebben ontvangen.Wil je meer informatie over deze en/of andere posities, neem dan direct contact op met Jan-Willem Broekhoven via nummer 020-5221333 en stuur je CV via de link op deze pagina.Huxley Associates Food is gespecialiseerd binnen de verschillende niches in de voedingsmiddelen industrie. - Productie/operationeel,- Planning,- Inkoop,- Sales and#38; Marketing,- QA/QC (HSE),- Rand#38;D/procestechnologie,- Maintenance.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technisch Inkoper, Helmond]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE51DAE8904F2A957482579F5001C0769</referencenumber>
<City><![CDATA[Limburg]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Technisch-Inkoper-Helmond_1664336.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een klant in de omgeving van Helmond ben ik op zoek naar een Technisch Inkoper. Je bent verantwoordelijk voor de inkoopprocessen en je optimaliseert de contracten en afspraken met leveranciers. Je werkt hierbij samen met productie afdelingen om zo tot een goed resultaat te komen. Je bent een ster in onderhandelen en hebt ervaring met sourcing en inkoop op internationaal niveau. Profiel:- je hebt 2 tot 5 jaar werkervaring in een gelijke functie- je hebt ervaring bij een bedrijf in consumentenproducten- je bent HBO/WO opgeleid- je hebt een sterke affiniteit met techniekVoldoe je aan bovenstaand profiel en heb je interesse? Stuur je CV via de link naar me toe!   and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Logistiek Leider, Geldermalsen, 3PL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob59E4DF1351073CAD482579F5001C0774</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Logistiek-Leider-Geldermalsen-3PL_1664337.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een grote speler binnen de consumer electronics branche in de omgeving van Geldermalsen ben ik op zoek naar een Logistiek Leider. In deze functie ben je verantwoordelijk voor de verzending van de producten en zorg je voor het logistieke proces hieromheen waaronder reverse logistics en voorraadbeheer. Ik ben op zoek naar iemand die zowel analytisch is als operationeel. Profiel:- affiniteit met consumer electronics- MBO logistieke opleiding- 2 tot 3 jaar werkervaring - Ervaring binnen een 3PLHeb je interesse en voldoe je aan bovenstaand profiel? Stuur je CV via de link naar me toe.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Procurement ManagerInternationalcirca £60,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2749653254D77EA2482579F5001C0781</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Procurement-Manager-International-circa-and-amp-SHARP16360000_1664338.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Do you want to working for a market leading manufacturing organisation? Have you had global exposure and responsibilities?The ideal candidate will currently be working in a global business, working with a huge multi million pound spend over a very small number of products. You will have good eye for contracts and understand legal implications. This is an excellent opportunity for a senior procurement professional with a strong and successful track record of strategic contract negotiation. This is a business critical role offering career progression in the future to Procurement Director.As much as 50% of your time will be spent travelling to areas such as Australia, Russia, Europe, and the United States and#38; Asia. To apply you will need an up to date CV.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Logistiek Supervisor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob56AF8FABB8ED0EE6482579F5001C078E</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Logistiek-Supervisor_1664339.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een grote speler in de retailbranche zijn wij op zoek naar een logistiek supervisor voor de productieafdeling van een distributiecentrum in de omgeving Den Bosch.Als logistiek supervisor ben je verantwoordelijk voor het volgende:- aansturing van je teamleiders, en indirect tussen de 50 en 170 magazijnmedewerkers;- het goed functioneren van je afdelingen;- zorgdragen voor de dagelijkse productieplanning, kwaliteit, managementinformatie, periodieke budgetopstelling en bewaking daarvan alsmede de opvolging van het ziekteverzuim;- deelname aan diverse vergaderingen;- rapportage aan de Logistiek Manager.Functieprofiel ideale kandidaat:- MBO+/HBO opleiding, bij voorkeur in logistieke richting;- enkele jaren relevante werkervaring;- aantoonbare leidinggevende ervaring;- goede communicatieve vaardigheden;- stressbestendig, besluitvaardig en passie voor het vak.Interesse? Reageer dan via de onderstaande link met een up-to-date CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supervisor Warehouse, Amersfoort, Retail]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6482229653287288482579F5001C079B</referencenumber>
<City><![CDATA[Amersfoort]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supervisor-Warehouse-Amersfoort-Retail_1664340.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een retail organisatie in de omgeving van Amersfoort ben ik op zoek naar een Warehouse Supervisor. In deze functie stuur je het warehouse personeel aan en zorg je ervoor dat het operationele proces gestructureerd en efficient verloopt. Je bent verantwoordelijk voor het formeren van een goed functionerend team, bewaakt het beleid, procedures en richtlijnen en ziet toe op de naleving hiervan. Je bent voortdurend bezig met het optimaliseren van de werkprocessen en rapporteert hierbij aan de Warehouse Manager. Functie-eisen- MBO / HBO opleiding in logistiek en transport- kennis van logistieke processen- 2- max 3 jaar leidinggevende ervaringVoldoe je aan bovenstaand profiel en heb je interesse? Stuur je CV via de link naar me toe!  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Teamleider Logistiek, Amsterdam en Utrecht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF66BC62C261A4404482579F5001C07AA</referencenumber>
<City><![CDATA[Amsterdam]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Teamleider-Logistiek-Amsterdam-en-Utrecht_1664341.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een retail organisatie in de omgeving van Amsterdam en Utrecht ben ik op zoek naar een teamleider logistiek. In deze functie stuur je de installateurs en chauffeurs aan en zorg je ervoor dat de service naar de klant toe geoptimaliseerd wordt. Je motiveert hiervoor circa 35 mensen en bent daarbij verantwoordelijk voor KPIand#146;s zoals kosten, klanttevredenheid, productiviteit en servicegraad. Je bent voortdurend bezig met het optimaliseren van de werkprocessen en beheert het wagenpark. Functie-eisen- MBO opleiding in logistiek en transport- kennis van logistieke processen- 2- max 3 jaar leidinggevende ervaringVoldoe je aan bovenstaand profiel en heb je interesse? Stuur je CV via de link naar me toe!  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Logistiek Supervisor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBC3E60F6085D7976482579F5001C07B7</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Logistiek-Supervisor_1664342.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor onze opdrachtgever zijn wij op zoek naar een logistiek supervisor voor de productieafdeling van een distributiecentrum in de omgeving van Utrecht.Als logistiek supervisor ben je verantwoordelijk voor het volgende:- aansturing van je teamleiders, en indirect tussen de 60 en 160 magazijnmedewerkers;- het goed functioneren van je afdelingen;- zorgdragen voor de dagelijkse productieplanning, kwaliteit, managementinformatie, periodieke budgetopstelling en bewaking daarvan alsmede de opvolging van het ziekteverzuim;- deelname aan diverse vergaderingen;- rapportage aan de Logistiek Manager.and#60;band#62;Functieprofiel ideale kandidaat:and#60;/band#62;- MBO+ opleiding, bij voorkeur in logistieke richting;- enkele jaren relevante werkervaring;- aantoonbare leidinggevende ervaring;- goede communicatieve vaardigheden;- stressbestendig, besluitvaardig en passie voor het vak.Interesse? Reageer dan via de onderstaande link met een up-to-date CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supervisor Logistiek, Tiel, 45k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1C8C61514EBEB4BB482579F5001C07C2</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supervisor-Logistiek-Tiel-45k_1664343.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een groot distributiecentrum in de omgeving van Tiel ben ik op zoek naar een supervisor logistiek. Je stuurt indirect tussen de 50-150 medewerkers aan. Je bent verantwoordelijk voor de productieplanning. Profiel:- MBO/HBO opgeleid- 3-5 jaar ervaring in leidinggeven in een soortgelijke functie- Communicatief vaardig- Affiniteit met consumer electronics Heb je interesse, voldoe je aan bovenstaand profiel en wil je meer informatie? Stuur je CV via de link naar me toe.  and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Production Planner  Materials Requirements]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3B802B542F58CFCB482579F5001C07D1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Production-Planner-Materials-Requirements_1664344.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading manufacturing company based in the Plymouth area to recruit a Production Planner to join the team.  We are looking for someone who can provide Planning support for their factory,  working for the logistics team (Central Planning) but also working closely with other business managers.You will be responsible for aligning plans for material requirements, provide factories and purchased stores with planned parts requirements which are aligned to lead-times, ensure the delivery of purchase and manufactured parts to meet build plans, ensure stock levels are maintained and ensure the ERP system is kept up to date to reflect ongoing process. To be be considered it is expected you will have Planning experience in a complex production environment,  ideally you will have received formal training in Production Planning and Control and will have experience of working with ERP systems.For immediate consideration please reply with your updated CV and contact detailsDuration: PermanentLocation: PlymouthSalary: Negotiable.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[IT Buyer  Purchasing  IT Systems  Gloucestershire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7AD7B1BD0EE44B79482579F5001C07DC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/IT-Buyer-Purchasing-IT-Systems-Gloucestershire_1669839.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are recruiting for an IT Buyer to join a successful organisation in the Gloucestershire area.  We are looking for someone who has worked in a purchasing role for IT software and Hardware systems.  They work with all the big names and partner with them to ensure they can deliver the best services across the market.  You will join their large purchasing team and take responsibility for a few category areas working with supplier to reduce costs and manage key relationships.To be considered you will have:- A few years experience in a buying / purchasing role. - Experience in purchasing IT Systems and comms- Strong skills in managing supplier relationships- Good negotiation skills For immediate consideration please reply NOW with your updated CVand#163;30,000 - and#163;35,000 + benefits.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Production Planner  Materials Scheduler  Plymouth]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF4D442CAB6F45CE3482579F5001C07E8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Production-Planner-Materials-Scheduler-Plymouth_1669840.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Huxley Associates are working with a leading manufacturer in Plymouth to recruit an experienced Production Planner / Materials Scheduler to join their team.Your role will involve aligning materials requirements to manufacturing schedules,  providing suppliers and stores managers with planned parts requirments, manage the delivery of parts to meet the manufacturing schedule, raise shortage and quality issues, minimise stock levels without impacting on delivery to reduce the amount of money tied up in stock , make sure ERP system planning data is kept up to date and raise change notes where required. We are looking for someone with proven experience of managing production materials schedules in a complex production environment.  Ideally you will have had some formal training in Production Planning and Control.  Finally it is expected you will have used MRP and supporting IT systems such as Excel.APPLY NOW]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior BuyerEast Midlandscirca £30,000£45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEA78FC190FC253D5482579F5001C07F4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Buyer-East-Midlands-circa-and-amp-SHARP16330000-and-amp-SHARP16345000_1669841.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Our client, a leading UK manufacturer based in the East Midlands currently requires a senior buyer. This is an excellent opportunity to take a step up in your career as this role will give you the opportunity for progression internally also.  Due to changes in the market and industry sector Procurement has now become a much more vital division within this business. My client is seeking a buyer with a strong strategic and project driven background ideally in a manufacturing environment. Whilst you will not have man management responsibility this is your chance to become a real leader in the team. To be successful in this role you will have worked in a fast paced manufacturing environment such as automotive etc. If you have experience in electronics, LEDs, plastics, metals, wood or overall raw materials then this will be extremely advantageous due to the level of in-house manufacturing taking place on site in the UK.   This is a fast paced environment where the possibility of change is highly likely.You must be adaptable to change but also have the ability to properly manage these changes effectively. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain ManagerWest Midlands circa £45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2897D6D1C09EFDD6482579F5001C07FF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Manager-West-Midlands-circa-and-amp-SHARP16345000_1669842.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Would you like the opportunity to join a world-leading company and become a key player in their business?Huxley Associates are delighted to be recruiting for a global manufacturer with excellent opportunities for progression both at home and abroad. To be considered for this role you will need to have a strong inventory management background with a strong focus on supplier development. You will be required to lead, develop and mentor a team of 4 people and therefore must have superb leadership experience and qualities. This role has become available due to a new business transformation plan and gives you the chance to be involved in the further development of this business division. As this is a Supply Chain role you should have excellent MRP knowledge. Much of this role will be about process improvement around supply chain principles including material flow, NPI and throughput efficiency.  This fantastic opportunity will suit an existing Supply Chain Manager, Inventory Manager or Logistics Manager who currently holds a and#147;hands onand#148; strategic role within a manufacturing organisation.  The successful applicant will be a problem solver with excellent analytical skills and the business acumen and awareness to spot potential opportunities. In addition to securing one of the best opportunities in the market you will be provided with some exceptional opportunities to develop your career on a local and international scale.If this sounds like you and you are interested in progressing, please send an updated copy of your CV.and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Operations Manager Air Freight]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA53BB9FF1BB180BD482579F5001C080B</referencenumber>
<City><![CDATA[Amsterdam]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Operations-Manager-Air-Freight_1669843.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Voor een grote logistieke dienstverlener in de omgeving van Amsterdam, zijn wij op zoek naar een Operations Manager voor de luchtvrachtafdeling.In deze rol ben je verantwoordelijk voor alle operationele activiteiten binnen de afdeling Air Freight. and#60;band#62;Verantwoordelijkheden:and#60;/band#62;- direct leiding geven aan de supervisors en indirect aan alle medewerkers;- budgetmanagement;- commercieel technische ondersteuning geven aan de verkoopafdeling;- proactief opstellen en uitvoeren van verbeterplannen t.b.v. de productiviteit en kwaliteit van de dienstverlening;- opmaken van performance rapportages. and#60;band#62;Functieprofiel ideale kandidaat:and#60;/band#62;- afgeronde HBO opleiding, bij voorkeur in logistieke richting;- aantal jaren relevante werkervaring binnen freight forwarding;- aantal jaren relevante aantoonbare leidinggevende ervaring;- operationele kennis en inzicht in freight forwarding (air en ocean), logistiek en supply chain management;- kennis van LEAN en 5S;- kennis van administratieve processen;- marktkennis van de logistieke dienstverlening, concurrentie, kansen en mogelijkheden;- goede kennis van de Engelse taal in woord en geschrift;- ervaring met MS Word, Excel en Powerpoint;- affiniteit met IT systemen.Interesse? Reageer dan via de onderstaande link met een up-to-date CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Planning ManagerWest Mids£42,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob878791293360E717482579F5001C0821</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Planning-Manager-West-Mids-and-amp-SHARP16342000_1669844.html</url>
<company><![CDATA[Huxley Associates]]></company>
<description><![CDATA[Would you like the opportunity to join a world-leading company and become a key player in their business? Huxley Associates are delighted to be recruiting for a global manufacturer with excellent opportunities for progression both at home and abroad. To be considered for this role you will need to have a strong inventory management background with a strong focus on supplier development. You will be required to lead, develop and mentor a team of 4 people and therefore must have superb leadership experience and qualities. This role has become available due to a new business transformation plan and gives you the chance to be involved in the further development of this business division. As this is a Supply Chain role you should have excellent MRP knowledge. Much of this role will be about process improvement around supply chain principles including material flow, NPI and throughput efficiency.  This fantastic opportunity will suit an existing Supply Chain Manager, Inventory Manager or Logistics Manager who currently holds a and#147;hands onand#148; strategic role within a manufacturing organisation. The successful applicant will be a problem solver with excellent analytical skills and the business acumen and awareness to spot potential opportunities. In addition to securing one of the best opportunities in the market you will be provided with some exceptional opportunities to develop your career on a local and international scale. If this sounds like you and you are interested in progressing, please send an updated copy of your CV. and#60;Br/and#62;and#60;Br/and#62;(Huxley Associates Limited acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Transport and Logistics</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager in Baden  Württemberg gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE3749F29829824D9482579F5001FA956</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Wrttemberg]]></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-in-Baden-and-amp-SHARP150-W-and-amp-SHARP252rttemberg-gesucht_1641087.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Aktuell suche ich fand#252;r ein mittelstand#228;ndisches, international tand#228;tiges Unternehmen der Medizintechnik einen Manager im Bereich Regulatory Affairs. Gesucht werden sowohl Mitarbeiter mit einschland#228;giger Berufserfahrung als auch Berufseinsteiger mit ersten Erfahrungen aus diesem Bereich.Zu Ihren Aufgaben gehand#246;rt die Planung, Durchfand#252;hrung und Betreuung von Zulassungsprozessen sowie die Erstellung der relevanten Dokumente. Sie werden verantwortlich fand#252;r die Koordination und Einhaltung der notwendigen nationalen und internationalen Regularien sein, und darand#252;ber hinaus Ansprechpartner fand#252;r jegliche Fragen aus diesem Bereich sein. Des Weiteren gehand#246;rt auch die and#220;berprand#252;fung der Vertriebsfand#228;higkeit der Produkte zu Ihren Aufgaben.Idealerweise haben Sie ein technisches Studium erfolgreich abgeschlossen, und bereits erste Erfahrungen in der praktischen Umsetzung und Pflege von Zulassungen gesammelt. Zu Ihren Qualifikationen zand#228;hlen sehr gute Englischkenntnisse sowie gute MS-Office-Kenntnisse. Ihr Profil wird durch Ihre Kommunikationsstand#228;rke, Durchsetzungsvermand#246;gen und Ihre Teamfand#228;higkeit abgerundet.Habe ich Ihr Interesse geweckt? Dann zand#246;gern Sie nicht, und kontaktieren mich!Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior QA Manager (Engineering)  Illinois]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7625BE8A9D9A9B04482579F5001FA962</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-QA-Manager-Engineering-Illinois_1641099.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Senior QA Manager (Engineering) - IllinoisSUMMARYMy client are looking for a Senior QA Manager with an Engineering background.The Senior Manager Quality Engineering at Libertyville, IL is responsible for managing a team of Quality Engineering professionals and for providing guidance on the application of Design Controls for project teams based at the Libertyville facility.  The Senior Manager provides guidance on the application of Quality and Reliability Engineering methods to groups and project teams at all facilities. RESPONSIBILITIESProvide guidance to corporate project teams with the application of Design ControlsLead Risk Analysis activities for evaluation of the product design.and#149;Facilitate the Risk Assessment meeting to evaluate the safety of a product design or design change, and to determine methods to eliminate or mitigate hazards.and#149;Document results.Work with NPD, Rand#38;D, and/or TSG on product design verification and validation activities.and#149;Participate in the development of the Traceability Matrix, which includes the product design Verification and Validation Plans.Work with the Plant QA managers to coordinate Plant Quality Engineering activities with corporate quality strategiesand#149;Communicates with QA managers regarding corporate QE strategies.and#149;Negotiates needed resubmissions or adjustments to documentation with plant and corporate management.Manages preproduction and first article processes at the corporate headquarters for evaluation, approval, and maintenance of recordsand#149;For First Articles, and for Preproductions that are not fully approved at the plant level:and#149;Coordinate evaluation process with required departments.Negotiates needed resubmissions or adjustments to documentation with plant and corporate management.Change/Work Request Systemand#149;When assigned and appropriate, review C/WRs and provide guidance on necessary deliverables.and#149;Collaborate with the C/WR project leader regarding any required test plans, experimental design, evaluation of data.and#149;Participate in the design control process, if required.and#149;Interface with the plants (QM, QE) to ensure plant perspective and requirements are taken into account.Product drawing evaluation and approvaland#149;Evaluate design to determine requirements for QA check points.and#149;Evaluate documentation for correctness.and#149;Alternate for product specification and ECN approval panels in QUMAS.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager of Quality Engineering  Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8DE5407C0BC445C9482579F5001FA96E</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Manager-of-Quality-Engineering-Medical-Devices_1641100.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Senior Manager Quality EngineeringSUMMARYThe Senior Manager Quality Engineering at Libertyville, IL is responsible for managing a team of Quality Engineering professionals and for providing guidance on the application of Design Controls for project teams based at the Libertyville facility.  The Senior Manager provides guidance on the application of Quality and Reliability Engineering methods to groups and project teams at all facilities. QUALIFICATIONSAcademic/Credentials/Certifications:B.S. Degree in Engineering or other related technical fieldLength of Experience:and#149;Minimum of 10 years of experience in supervision (management of quality engineering associates required)and#149;Minimum of 10 years in the quality fieldand#149;Minimum of 10 years in the medical products industry (medical device industry preferred)Specialized Skills/Technical Knowledge:ASQ Certified Quality EngineerASQ Certified Reliability EngineerKnowledge of applicable standards and regulations:- cGMP/21CFR820- EU MDD 93/42/EEC- ISO 14971- ISO 13485: 2003Ability to read and interpret product drawings and to set up and perform statistical and dimensional analyses.Preferred:MS in Technical Management, Statistics, or MBALicensed PEExperience in statistics, instrumentation, molding, electronicsAdvanced QA coursesExperience with electronic medical devicesExperience with plastics, films, and moldingOther Certifications:- Certified Quality Manager- Certified Software Quality Engineerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer  Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob75BF0DB37700EFFB482579F5001FA97B</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Engineer-Medical-Devices_1641101.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients, a world renown Medical Device company based in Libertyville, Chicago are looking for a Senior Quality Engineer to join their company. The Senior Quality Engineer will need to have a strong background in QA as well as a good education and will also have excellent communication skills. QUALIFICATIONS  Academic/Credentials/CertificationsB.S. Degree in Engineering or Engineering in Technology, or equivalent Length of experienceMinimum two years as a Quality Engineer in addition to four years industry experience in a quality related field. Specialized skills/technical knowledgeLaboratory expirenceAble to read and interpret product drawingsAble to set-up and perform dimensional analysisand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD58D6CD6BF46D7F0482579F5001FA985</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Quality-Engineer_1641102.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance Engineer supports new product development in Raw Material selection and qualification. Global cost saving projects on new Raw Materials and Global projects on harmonisation across plants on quality standards within own responsibility arear.The Quality Engineer is involved in vendor evaluation, qualification and performance as well as optimizing Raw materials Performance and Quality.Optimize current laboratory rutines, incomming inspection and Test methods in the QA lab. RESPONSIBILTIESSupport New Product Development (Raw Materials):   50%a) Represent Quality Management on product development teams (Raw Materials)b) Ensure that quality and reliability in current Test Methods and implementation of new  Test Methods in QA Laboratory. c)  Ensure that documentation is updated and new procedures implemented.d)  Coordinate raw materials inspection documents and training with the Raw Material Teame)  Assist with 0-series and +1 series review.f)  REACH and#150; update corporate document. Global projects and cost saving initiatives:   20%a) Review new CWR on new mateials for safety/ tox, efficacy, and reliability issues.b) Review the plan and results for new material qualification.Optimize Existing Raw Material Quality:   20%a) Provide material performance analysis based on Production input and venror performanceb) Perform internal audits and help to continuously improve the quality system.Vendor Evaluation and Performance:   10%a) Interface with other corporate departments and the plants to develop new potential vendors and assure their acceptabilityb) Participate in resolving specification questions leading to acceptance of Hollister specifications by vendorsc) Identify and communicate to the involved corporate departments information about the performance of existing vendors.  Recommend any necessary corrective actions.d)  Perform audits of potential and existing vendors, and rate their level of acceptability.If you want to apply - send over your resume today.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer  Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB46926A64A6162BC482579F5001FA992</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Engineer-Medical-Devices_1651706.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients, a world renown Medical Device company based in Libertyville, Chicago are looking for a Senior Quality Engineer to join their company. The Senior Quality Engineer will need to have a strong background in QA as well as a good education and will also have excellent communication skills. QUALIFICATIONS  Academic/Credentials/CertificationsB.S. Degree in Engineering or Engineering in Technology, or equivalent Length of experienceMinimum two years as a Quality Engineer in addition to four years industry experience in a quality related field. Specialized skills/technical knowledgeLaboratory expirenceAble to read and interpret product drawingsAble to set-up and perform dimensional analysisand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Statistiker mit Karrierechancen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3EB4129622862E5C482579F5001FA99E</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Statistiker-mit-Karrierechancen_1658682.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mand#246;chten Sie tagtand#228;glich Ihr Bestes geben und daneben Ihre Karriere vorantreiben indem Sie immer mehr dazulernen und dies von den Besten auf Ihren Gebiet? Dann ist diese Stelle genau das Richtige fand#252;r Sie!Das Unternehmen zand#228;hlt zu den grand#246;and#223;ten Arbeitgebern auf ihrem Bereich in der Region Basel und beschand#228;ftigt rund 5.000 Mitarbeiter. Mit dem Ziel tagtand#228;glich ihr Bestes zu geben setzt sich mein Kunde hohe Ziele um die Lebensqualitand#228;t tausender Patienten zu verbessern. Um die hohe Qualitand#228;t zu gewand#228;hrleisten setzt das Unternehmen vor allem auf seine Mitarbeiter in die sie sehr viel investieren. Von Mentorenprogrammen and#252;ber Coaching, sei es intern oder extern, wird sichergestellt, dass die Mitarbeiter den Patienten die bestmand#246;gliche Versorgung bieten kand#246;nnen.Um auch in Zukunft die hohe Qualitand#228;t bieten zu kand#246;nnen und die wachsenden Patientenzahl  behandeln zu kand#246;nnen sucht mein Kunde einen Senior Statistiker um das Epidemiologie und Statistiker Team zu unterstand#252;tzen.Das Unternehmen sucht einen Bewerber / eine Bewerberin mit einem Abgeschlossenen Medizinstudium oder einem Studium im verwandten Bereich. Weiterhin sind einige Jahre Erfahrung wand#252;nschenswert. Daneben sollten Sie sicher im Umgang mit SAS und / oder R sein und bereits erste Erfahrung mit der Fand#252;hrung von Teams gesammelt haben. Der richtige Bewerber ist weiterhin flieand#223;end in Englisch und kann sowohl Artikel auf Englisch verfassen als auch die Studienresultate auf Englisch prand#228;sentieren. Deutsch wand#228;re von Vorteil.  Mein Kunde bietet Ihnen ein sehr internationals Arbeitsumfeld in einem sehr internationalen Team. Das Team besteht momentan aus 3 Statistikern in einer Abteilung in der 20 Mitarbeiter arbeiten. Daneben bietet das Unternehmen sehr gute Karrieremand#246;glichkeiten, sowie stetige Weiterbildungen. Sei es internes und / oder externes Coaching oder Mentorenprogramme and#150; Bei diesem Unternehmen lernen Sie von den Besten auf Ihren Gebiet. Ich arbeite als Recruitment Consultant fand#252;r Real Pharma und bin fand#252;r den Bereich Biometrik und HEOR innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 435080972 zu erreichen. Ansonsten kand#246;nnen Sie mich auch gerne unter k.schirmer(at)realstaffing.com kontaktieren. Keywords: Epidemiologie, Epidemiology, Suisse, Schweiz, Switzerland, German, English, Deutsch, Englisch, Life Science, Basel, Biostat, Biostatistik, Biostatistician, Statistician, Klinische Forschung, clinical study, klinische Studie, Qualitand#228;t, Healthcare, Patienten, Patients, Karriere, Basel Stadt, BS, Basel Land, BLand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Entwickler Medizintechnik Hamburg Sofort zu besetzen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA37CC0824727ACEC482579F5001FA9B7</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Entwickler-Medizintechnik-Hamburg-Sofort-zu-besetzen_1641120.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist in Norddeutschland und in der Medizintechnik ansand#228;ssig. Das Unternehmen ist global tand#228;tig und bereits auf eine sehr langen Firmengeschichte zurand#252;ckgreifen. Aufgrund der stetigen Nachfrage nach deren Produkten, benand#246;tigt mein Kunde fand#252;r den schnellstmand#246;glichen Zeitpunkt einen Software Entwickler.Software-EntwicklerIhre Aufgaben:Sie sind fand#252;r Kleinprojekte verantwortlichSie betreuen zusand#228;tzlich externe DienstleisterEntwicklung von Computer-Softwareland#246;sungen C/C++ and#38; C# fand#252;r die MedizintechnikVerantwortlich fand#252;r Modul- und Test-StrategieErstellung von SpezifikationenIhr Profil:Studium der Informatik o. and#228;. Erfahrung in C/C++Erfahrung in C# und .NET Sie sollten ebenfalls Kenntnisse in grafischen Benutzeroberfland#228;chen besitzen sowie in SQL- DatenbankenBerufserfahrung ist wesentlich von VorteilSie mand#246;chten in einem Traditionsunternehmen neu Fuand#223; fassen? Sie wand#252;nschen sich Respekt und Anerkennung?Dann bewerben Sie sich jetzt als Software Entwickler!Schicken Sie mir umgehend Ihr CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Clinical Trial Assistant  Bayern  1.0 FTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA04D5D23CD093FCC482579F5001FA9C3</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Clinical-Trial-Assistant-and-amp-SHARP150-Bayern-10-FTE_1641137.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is an international specialty Pharma Company in the heart of Bayern with a truly great environment to work in. They are currently seeking a Freelance Clinical Trial Assistant for 6 months+. The role offers a great opportunity for those who may be looking for a new challenge in life. You should also have a very strong interpersonal skills and good experience in the Clinical Research area. Also excellent organizational and time management skills are required. Key Responsibilities:and#149;Is responsible for writing Agenda and#38; Minutes and#149;Support in organization of meetings and#149;Assists in the coordination of activities to ensure CRO and vendor delivery against the contracted scope of   work and#149;Provide practical support to the Clinical Operations group in the set up of the administration for the management of Clinical Trials and#149;Filing/archiving of documents in-house in line with GRT SOPand#146;s in close operation with the Clinical Trial Documentation and Archiving Unit and#149;Assist in ensuring that trial related documentation is accurate and up to date and#149;Assist in ordering trial related material and#149;Is responsible for tracking of all trial related information (e.g. CTMS)  Expertise and Complexity:and#149;Clinical experience preferredand#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilitySalary/ Duration:and#149;Negotiableand#149;Start 01.06.2012and#149;End  01.12.2012 (with option on extension)As a specialist recruiter in Clinical Research positions for Pharmaceutical clients in Germany and Switzerland, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.Apply now! Call Parminder Singh at +49 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Business Intelligence Analyst  Hull  Circa. £40K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3D65C59FED263C17482579F5001FA9D4</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Global-Business-Intelligence-Analyst-Hull-Circa-and-amp-SHARP16340K_1641247.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Global Business Intelligence and#150; Hull and#150; Major Healthcare Company  and#60;/band#62;The GBI team is responsible for strategic intelligence support and competitor intelligence provided primarily to Group staff, covering all of the major OTC categories. and#60;band#62;Scope of Roleand#60;/band#62; The role interfaces with all parts of the organisation  and#150; both inward-facing in its focus on  own brands and outward focused in tracking competitor / industry activity. The BI function, and outputs of their analysis, acts as an early warning system of competitor and industry activity, highlighting potential opportunities and threats. Learningand#146;s, conclusions and findings often input to key changes in RB processes, organisation and strategy.and#60;band#62;Responsibilitiesand#60;/band#62; Project-based research and analysis: Undertake a wide range of project-based requests from senior management. These can vary in length, subject and level of analysis required, but typically involve accessing different sources, validating and challenging data; delivering the output/conclusion in presentation formatTracking and reporting competitor innovation and key activitiesStrategic Planning: Work on internally focused projects such as Portfolio Analysis, forecasting opportunity sizes and assessing potential of new geographies.Benchmarking: Analyse key financials for competitive set and report regularly on performance. and#60;band#62;Experienceand#60;/band#62;Honours Degree  - either: 2 / 3 years experience in OTC Healthcare / Pharmaceuticals and#150; within a business / competitor / intelligence function OR consulting OR Strategic Planning.Experience of working within (or adjacent to) an international marketing environment would be useful. and#60;band#62;Skillsand#60;/band#62;and#149; Excellent analytical skills and#150; ability to scope and structure complex data and present and visualise the findings and conclusions at a strategic level.and#149; Ability to work with unstructured information from a wide variety of sources and synthesise in a highly summarised strategic format.and#149; Experience in working with and analysing large data sets is essential and#150; previous modelling, statistical analysis project would be useful.and#149; High level Excel skillsand#149; Familiarity with key elements of company Pand#38;Ls and financial ratios.and#149; Ability to manage and prioritise the ongoing monitoring / tracking activities required within GBI vs project demands.For further information contact Sarra Gwilym on 0207 758 7311 or forward your CV for direct application.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Statistiker mit Karrierechancen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1ABF3F5AE13A9B9A482579F5001FA9E3</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Statistiker-mit-Karrierechancen_1641300.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mand#246;chten Sie tagtand#228;glich Ihr Bestes geben und daneben Ihre Karriere vorantreiben indem Sie immer mehr dazulernen und dies von den Besten auf Ihren Gebiet? Dann ist diese Stelle genau das Richtige fand#252;r Sie!Das Unternehmen zand#228;hlt zu den grand#246;and#223;ten Arbeitgebern auf ihrem Bereich in der Region Basel und beschand#228;ftigt rund 5.000 Mitarbeiter. Mit dem Ziel tagtand#228;glich ihr Bestes zu geben setzt sich mein Kunde hohe Ziele um die Lebensqualitand#228;t tausender Patienten zu verbessern. Um die hohe Qualitand#228;t zu gewand#228;hrleisten setzt das Unternehmen vor allem auf seine Mitarbeiter in die sie sehr viel investieren. Von Mentorenprogrammen and#252;ber Coaching, sei es intern oder extern, wird sichergestellt, dass die Mitarbeiter den Patienten die bestmand#246;gliche Versorgung bieten kand#246;nnen.Um auch in Zukunft die hohe Qualitand#228;t bieten zu kand#246;nnen und die wachsenden Patientenzahl  behandeln zu kand#246;nnen sucht mein Kunde einen Senior Statistiker um das Epidemiologie und Statistiker Team zu unterstand#252;tzen.Das Unternehmen sucht einen Bewerber / eine Bewerberin mit einem Abgeschlossenen Medizinstudium oder einem Studium im verwandten Bereich. Weiterhin sind einige Jahre Erfahrung wand#252;nschenswert. Daneben sollten Sie sicher im Umgang mit SAS und / oder R sein und bereits erste Erfahrung mit der Fand#252;hrung von Teams gesammelt haben. Der richtige Bewerber ist weiterhin flieand#223;end in Englisch und kann sowohl Artikel auf Englisch verfassen als auch die Studienresultate auf Englisch prand#228;sentieren. Deutsch wand#228;re von Vorteil.  Mein Kunde bietet Ihnen ein sehr internationals Arbeitsumfeld in einem sehr internationalen Team. Das Team besteht momentan aus 3 Statistikern in einer Abteilung in der 20 Mitarbeiter arbeiten. Daneben bietet das Unternehmen sehr gute Karrieremand#246;glichkeiten, sowie stetige Weiterbildungen. Sei es internes und / oder externes Coaching oder Mentorenprogramme and#150; Bei diesem Unternehmen lernen Sie von den Besten auf Ihren Gebiet. Ich arbeite als Recruitment Consultant fand#252;r Real Pharma und bin fand#252;r den Bereich Biometrik und HEOR innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 435080972 zu erreichen. Ansonsten kand#246;nnen Sie mich auch gerne unter k.schirmer(at)realstaffing.com kontaktieren. Keywords: Epidemiologie, Epidemiology, Suisse, Schweiz, Switzerland, German, English, Deutsch, Englisch, Life Science, Basel, Biostat, Biostatistik, Biostatistician, Statistician, Klinische Forschung, clinical study, klinische Studie, Qualitand#228;t, Healthcare, Patienten, Patients, Karriere, Basel Stadt, BS, Basel Land, BLand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs  North  £65k  Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4DC4D12A2164EF1B482579F5001FA9F4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-North-and-amp-SHARP16365k-Medical-Devices_1641328.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Main tasks (primary responsibilities) of the position: Direct and prepare regulatory submissions as required for global approvals for IVDand#146;s, including preparation of reports and interaction with regulatory officials as required Manage  a highly effective Regulatory Affairs function, with line management responsibility for Senior Managers Review product labeling and promotional literature for regulatory compliance Research and interpret regulations, guidelines and precedents to support interdepartmental project teams in developing strategies, policies and procedures that ensure regulatory compliance with global regulatory agencies  Interface with regulatory agencies for inquiries and issues Review Rand#38;D protocols and technical reports and other company documents (including labeling and marketing materials, when applicable) for use in regulatory submissions and in response to queries from regulatory authorities Oversee and direct the preparation of regulatory documentation for country-specific registrations Develop regulatory process SOPs relevant for registration of IVD products or other regulatory aspectsPosition requirements, qualifications and experiences: Extensive experience in the medical device industry, preferably with IVD experience, and extensive regulatory experience, preferably in the area of IVDs, including the preparation and submission of 510(k), PMAs, PLAs, ELAs, IND, IDE, CE Design Dossiers, CE Technical Files, and CLIA Certificate applications.   A proven ability to lead and influence colleagues successfully in a dynamic and evolving matrix environment. Possess a working knowledge of the MDD and IVDD, applicable ISO standards, and US medical device/IVD regulation.   Demonstrated organisational, planning and prioritising abilities, as well as strong technical writing ability;  Must be able to exercise sound judgment for high-level decision-making responsibilities]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Data Manager  Contract  Pharmaceutical  Illinois]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF7F7A8CF012C4746482579F5001FABAA</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago North]]></State>
<url>http://www.engineerjob.us/job/Clinical-Data-Manager-Contract-Pharmaceutical-Illinois_1641126.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a leading Contract Research Organization based in Illinois, now has a fantastic opportunity for Clinical Data Manager to work on a variety of projects across Oncology, CNS and Cardio within Phases II and III.  This is a 12 month contract paying and65 - and70 per hour.The market leading CRO is seeking to hire a talented Clinical Data Manager to work on the full lifecycle of the data management aspect of Clinical Trials within Phases II and III.  This will involve assisting with the creation of the SAP and data plans through to the Database Lock phase.Candidates for this position must have the following skills and experience:- Bachelors degree or higher within Computer Science or related field- 3+ years Data Management experience within Pharmaceutical Medical Device Companies- Proven track record in query creation and resolution- Database Lock experienceApply now for immediate consideration or contact Tom Bakker on 312-453-9088. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produktmanager   Pharma  BadenWürttemberg  ab sofort zu besetzen!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8399A1F50C6F94D5482579F5001FABC7</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Wrttemberg]]></State>
<url>http://www.engineer-job.eu/job/Produktmanager-and-amp-SHARP150-Pharma-and-amp-SHARP150-Baden-W-and-amp-SHARP252rttemberg-and-amp-SHARP150-ab-sofort-zu-besetzen_1641130.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mand#246;chten Sie in einem mittelstand#228;ndischen Unternehmen beschand#228;ftigt sein, indem and#188; des Umsatzes in Forschung und Entwicklung investiert wird? Mein Kunde ist mit seiner Produktpalette in mehr als 15 Land#228;ndern der Welt prand#228;sent und konzentriert sich auf Produkte u.a. aus dem Bereich der Onkologie.Sind Sie bereit, mit Ihrem Wissen, Ihrer Erfahrung und Ihrer Persand#246;nlichkeit den Firmenerfolg voranzutreiben und Teil eines familiand#228;ren Teams zu sein?Dann sollten Sie als Produktmanager im Pharmabereich Interesse haben.Idealerweise erfand#252;llen Sie als interessierter Kandidat folgende Kriterien:and#149; abgeschlossenes Studium der BWL oder der Naturwissenschaftenand#149; sehr gute Marketing-Kenntnisse, vor allem im strategischen Marketingand#149; Erfahrung innerhalb der Pharmaindustrieand#149; idealerweise haben Sie Ihre Industriekenntnisse im Bereich der Onkologie bzw.   Intensivmedizin gesammeltand#149; verhandlungssicheres Englischand#149; ReisebereitschaftBewerben Sie sich noch heute und warten nicht zu lange. Denn es gibt hier nur eine Stelle zu besetzen. Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Wir freuen uns auf Sie.Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CTA dringend gesucht für die Schweiz]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5C8A905B174B2889482579F5001FABD4</referencenumber>
<City><![CDATA[Switzerland All]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CTA-dringend-gesucht-f-and-amp-SHARP252r-die-Schweiz_1641189.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Unser Kunde ist ein fand#252;hrendes Unternehmen im Bereich Medical Devices. Das Unternehmen besitzt ein interkulturelles Netzwerk von Mitarbeitern in and#252;ber 80 Standorten weltweit. Am Schweizer Standort mand#246;chte das global agierende Unternehmen sein Clinical Operation Team erweitern und sucht daher einen engagierten Clinical Trial Assistant. Das Arbeitsumfeld ist sehr motivierend und liegt inmitten der schand#246;nen Schweizer Bergwelt, die Ski fahren, wandern und vieles mehr ermand#246;glicht.Die Clinical Trial Assistant Position ist eine sehr spannende und abwechslungsreiche Stelle im Clinical Operation Bereich, dies bedeutet, Sie werden das klinische Team mit verschiedensten unterschiedlichen administrativen Aufgabenbereichen unterstand#252;tzen, wie das Generieren von Daten, Vorbereitung von Dokumente und Protokollen, das Bearbeiten von Patientendaten und die Dokumentenpflege klinischer Akten. Zusand#228;tzlich bieten sich Aufstiegsmand#246;glichkeiten zum Lead CTA oder CRA durch interne Weiterbildungsmand#246;glichkeiten fand#252;r motivierte Mitarbeiter an.  Ein CTA-Kandidat sollte daher folgende Eigenschaften mitbringen wie einen universitand#228;ren Abschluss im Bereich klinischer Forschung oder in einem and#228;hnlichen Bereich, gute kommunikative Fand#228;higkeiten besitzen, sowie flieand#223;end deutsch und englisch sprechen, jede weitere Fremdsprache ist ein Plus. Des Weiteren sollten Sie ein motivierter und positiv denkender Mensch sein, der selbstand#228;ndig wie auch in einem internationalen Team arbeiten kann.Falls Sie sich angesprochen fand#252;hlen, dann senden Sie so schnell wie mand#246;glich Ihre aussagekrand#228;ftigen Bewerbungsunterlagen in Word Format  an Nadja Beckert n.beckert(at)realstaffing.com oder falls noch weitere Fragen haben die offen sind dann rufen Sie mich doch unter +41 (0)4350809728 an. Schweiz, Luzern, Zand#252;rich, klinische Studien, clinical Trial, Clinical Trial Assistant, klinische Projektassistenz, klinische Forschung, CRO, CPA, CRA, CTA, Pharmabereich, Switzerland, klinische Forschung, klinische Untersuchungen, Clinical Trial Assistant, klinische Mitarbeiter, SCRA, Senior CRA, Principal CRA, Kanton Zand#252;rich, Clinical Operation, Nadja Beckert, Studienbegleitung, Clinical Data Associate, Clinical Research Associates, Clinical Trial Manager, Clinical Studies, Study Managers, Klinisches Monitoring, Monitoring, CRO, CRA, Senior CRA, Senior CRO, Director Clinical Research, Head of Medical Studies, Head of Clinical Research, Clinical Project Managerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Engagierter Market Access Manager mit nationalem Fokus]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA5042CE1EC3A60C3482579F5001FABE1</referencenumber>
<City><![CDATA[Berne]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Engagierter-Market-Access-Manager-mit-nationalem-Fokus_1641198.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Aufgrund der aktuellen Marktsituation sehen sich aktuell viele Unternehmen der Herausforderung gegenand#252;ber ein sehr starkes und wettbewerbsfand#228;higes Team im Bereich Market Access und Pricing and#38; Reimbursement zu haben. Aktuell unterstand#252;tze ich die Schweizer Niederlassung eines der grand#246;ssten Pharmaunternehmen weltweit bei der Identifikation von Talenten in Bereich Market Access, Governmental Affairs und Public Relation. Fand#252;r dieses Unternehmen suche ich einenMarket Access Manager mit einem Schweizer FokusDie Hauptaufgaben innerhalb dieser Funktion belaufen sich vor allem auf + Aufbau und Pflege eines starken Netzwerkes mit key stakeholder speziell mit dem BAG und verschiedenen Krankenversicherungen+ Entwicklung und Implementierung von Market Access Strategien fand#252;r neue Indikationen+ Zusammenarbeit mit verschiedenen internen Abteilungen sowie externen Organisationen um eine wettbewerbsfand#228;hige Market Access Strategie zu gewand#228;hrleisten + Entwicklung und Implementierung einer Pricing Strategie + Market Access Trainings fand#252;r verschiedene interne Abteilungen Fand#252;r diese Position suche ich eine engagierte Persand#246;nlichkeit, die bereits Erfahrung im Bereich Market Access in der Schweiz gesammelt hat. Sollten Sie bereits Erfahrung und ein Netzwerk in der Schweiz haben wand#228;re dies von Vorteil. Da sich die Position auf Onkologie fokussiert, suche ich vor allem jemanden, der bereits Erfahrung in diesem Bereich hat. Neben Sprachkenntnissen in Deutsch, Englisch und Franzand#246;sisch sollten Sie weiterhin noch einen Universitand#228;ren Abschluss, gerne im Bereich (Health) Economic, Law, etc. mitbringen. Wenn ich Ihr Interesse fand#252;r diese Position oder weitere Positionen im Bereich Biometrik und HEOR geweckt habe, freue ich mich and#252;ber eine Kontaktaufnahme um mit Ihnen verschiedene Mand#246;glichkeiten hier in der Schweiz zu besprechen. Sie kand#246;nnen mich unter +41 435080972 oder k.schirmer(at)realstaffing.com erreichen.Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, Market Access, Pricing, Reimbursement, pharma, Multinational Enterprise, MNE, Oncology, Onkologieand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mitarbeiter für meine Kunden in der Pharmaindustrie gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2430949E7CC25CCF482579F5001FABEC</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mitarbeiter-f-and-amp-SHARP252r-meine-Kunden-in-der-Pharmaindustrie-gesucht_1641275.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Meine Kunden sind Pharmaunternehmen, die verschiedene Indikationen und Bereiche abdecken, einige hiervon sind z.B. auch bekannte Generika Unternehmen, forschende Pharmaunternehmen sind natand#252;rlich ebenfalls in meinem Kundenstamm vertreten.Aufgrund der guten Marktsituation und des Wachstums der Unternehmen sind derzeit einige Stellen vakant die ich gerne besetzten mand#246;chte. and#220;berwiegend sind derzeit  Key Account Manager Positionen zu besetzten, diese in den unterschiedlichsten Bereichen sowie Indikationen. Sowohl die Definition des Key Account Manager als Innendiestmitarbeiter, also in eine kaufmand#228;nnische Richtung gehend, ist derzeit bei meinen Vakanzen vertreten als auch die eher typischen Key Account Manager Position im Auand#223;endienst, die z.B. die Aufgaben der Betreuung von Spezialkunden beinhaltet. Zudem suche ich verstand#228;rkt Brand Manager sowie Product Manager mit RX und/oder OTC Erfahrung ( 2 and#150; 3 Jahre Berufserfahrung sind Grundvoraussetzung) mit flieand#223;enden, verhandlungssicheren Englischkenntnissen in Wort und Schrift. Sie suchen derzeit eine neue Herausforderung in der Pharmaindustrie? Haben Ihr Studium der Medizin, Naturwissenschaft, BWL oder vergleichbaren erfolgreich abgeschlossen? Bringen einige Jahre Berufserfahrung aus der Pharmaindustrie mit?Dann schicken Sie bitte Ihre Bewerbungsunterlagen an: Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400Bei Fragen stehe ich Ihnen gerne zur Verfand#252;gung.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Manager Medizintechnik (wm) nahe Mannheim gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob648C9B3C16F4B502482579F5001FABFB</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Pfalz]]></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Manager-Medizintechnik-w-m-nahe-Mannheim-gesucht_1641278.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Zum Aufbau- und weiteren Ausbau des Geschand#228;ftsbereiches Medizintechnik, Biotech und Pharmazie meines Kunden, ein stark international geprand#228;gtes Unternehmen nahe Mannheim, wird nand#228;chstmand#246;glich ein kompetenter Supply Chain Manager gesucht. and#60;/band#62;and#60;band#62;Ihre Aufgabenand#60;/band#62;Sie sind fand#252;r das komplette Supply Chain Management, dessen Gestaltung und stetige Weiterentwicklung verantwortlich. Der Einkauf von C-Artikeln, Rohstoffen etc. sowie  das Erstellen von Fertigungsauftrand#228;gen gehand#246;rt ebenfalls zu Ihren Aufgaben. Das Lagerbestandsmanagement sowie die Preisverhandlungen runden Ihr Portfolio ab. Sie sind die Schnittstelle zur Muttergesellschaft.and#60;band#62;Ihr Profiland#60;/band#62;Sie bringen ein abgeschlossenes Studium im Bereich Wirtschaftsingenieurwesen mit Schwerpunkt Maschinenbau oder Betriebswirtschaft mit Schwerpunkt Supply Chain Management mit. Erste Berufserfahrung and#252;ber einschland#228;gige Praktika oder ein abgeschlossenes Traineeprogramm sind von Vorteil. Technisches Verstand#228;ndnis bei der Weiterentwicklung des Bereiches Supply Chain Management sowie Interesse an Fand#252;hrungsverantwortung fand#252;r Mitarbeiter ist wand#252;nschenswert.Wenn Sie sich dieser verantwortungsvollen Aufgabe stellen mand#246;chten, senden Sie uns bitte Ihre aussagekrand#228;ftigen Bewerbungsunterlagen an folgende Kontaktdaten zu.  a.wydra(at) realstaffing.com / Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Medical Information Officer  £45k  Benefits, Berkshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCA610FD66DF97001482579F5001FAC06</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Senior-Medical-Information-Officer-and-amp-SHARP16345k-Benefits-Berkshire_1651660.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has an outstanding reputation and is a leader in its field. With its vast product portfolio and exciting pipeline, Medical Information is a key focus area.I am looking for someone of strong medical information experience to join a team with great cohesion, motivation and work ethic. Stability, training and excellent benefits are on offer to the right candidate.- Life Science degree - Good working knowledge of the Code of Practice (ABPI)- Copy approval experience preferably on zinc- Excellent oral and written English - To have been involved with delivering training to internal staff and understand the needs of the Field Force- To be able to handle telephone and written enquiriesThis is a varied role with the opportunity to be involved across the board for medical information depending on experience. If you feel you suit the vacancy please send an updated CV to Taran - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director for Market Access urgent required]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3402F92A0B9A8497482579F5001FAC12</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Associate-Director-for-Market-Access-urgent-required_1658698.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[With all the healthcare companies focusing on Switzerland companies in this industry are facing high competition. In this competitive world of healthcare sales it is important to have an excellent market access strategy. I am currently searching for one of my clients, a big, international health care company, a Market Access specialist with an international focus. I am searching for individuals with experience in market access in Switzerland and who are fluent in English and German, to be fluent in French would be an advantage. The company is offering you a position in a global, broad based health care company in an international team located in the German speaking part of Switzerland. Working for this company means that you will be working for a company which is recognised as a good place to work and which received numerous local, national and international distinctions. As the Market Access specialist you will act as an area leadership member regarding market access subjects and you would contribute to the area strategy and tactic plans. Additionally this position is responsible for identifying and developing payer solutions to establish and strengthen the portfolio proposition with target payer customers. This position is a strategic and new role which is responsible for setting the new course to create payer customer specific value.   I am a recruitment consultant working in Switzerland. I am specialised in HEOR, Market Access and Biometrics. If you want to get further information regarding this positions, or on many more like this, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com. I am looking forward to receiving your current CV as a word document.  Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, good place to work, international, pricingand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[International Market Access Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB86675B19740DA03482579F5001FAC21</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/International-Market-Access-Manager_1658701.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[With all the healthcare companies focusing on Switzerland companies in this industry are facing high competition. In this competitive world of healthcare sales it is important to have an excellent market access strategy. I am currently searching for one of my clients, a big, international health care company, a Market Access specialist with an international focus. I am searching for individuals with experience in market access in Switzerland and who are fluent in English and German, to be fluent in French would be an advantage. The company is offering you a position in a global, broad based health care company in an international team located in the German speaking part of Switzerland. Working for this company means that you will be working for a company which is recognised as a good place to work and which received numerous local, national and international distinctions. As the Market Access specialist you will be responsible for acting as a leadership member regarding market access subjects and you will contribute to the area strategy as well as to the tactic plans. Additionally the market access manager will be responsible for identifying and developing innovative payer solutions to establish and strengthen the portfolio of the company.  This position is a very senior position within the market access department, responsible for overseeing the overall market access operation. Additionally this position would play a critical role in shaping the market access department into a proactive and integrated function. I am a recruitment consultant working in Switzerland. I am specialised in HEOR, Market Access and Biometrics. If you want to get further information regarding this positions, or on many more like this, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com. I am looking forward to receiving your current CV as a word document.  Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, good place to work, international, pricingand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. Design Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE33862D69F488FC0482579F5001FBA57</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Design-Engineer_1651656.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Job Description:and#60;/band#62;and#149;Provide quality oversight for medical device products and drug delivery systems manufactured at CMOsand#149;Interact with contractors and CMOs and act as the face of quality for this organizationand#149;Support release of finished clinical and commercial productsoIncluding: batch record review, resolutions of investigations/quality issues and assessment of change controlsand#149;Develop and maintain quality risk management plans and device control documentationand#149;Participate in regulatory inspections/ compliance audits to ensure time management of CAPAsand#149;Act as SME and trainer on Quality Systems, standards and processesand#60;band#62;Job Requirements:and#60;/band#62;and#149;BS Degree - mechanical engineer is preferred (life science degree is also accepted)and#149;Quality Engineer with 10+ years of hand-on design control experience in the medical device, pharmaceutical, or diganostics industryand#149;Certified Quality Engineer is preferredand#149;Hands-on expertise in the following areas is required: aseptic filling/lyophilization, secondary packaging, and medical device/combination product manufacturingand#149;Must have experience with early development medical devices and#149;Solid understanding of ISO 13485:2003 and ISO 14971 is requiredand#149;Excellent communication skills both verbal and written; must have experience and confidence with speaking to high level Executivesand#149;Excellent interpersonal/people skillsand#149;Must be organized, prioritized and have excellent time management skills]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. Validation Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob54CC4480453B8C4F482579F5001FBA67</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Validation-Engineer_1651657.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Job Duties:and#60;/band#62;and#149;Oversee all management functions for the validation groupand#149;Manage the workload of the validation teamand#149;Provide strategy sessions for the groupand#149;Revise validation plansand#149;Act as main point of contact for other sites and corporate functions on behalf of the teamand#149;Approve all critical validations reportsand#149;Conduct root cause analysis, review problems, and present findings to the teamand#149;Participate in the risk management team and attend relevant meetingsand#60;band#62;Job Requirements:and#60;/band#62;and#149;BA/BS degree, requiredand#149;10-12 years of validation and management experience in the pharmaceutical/biotech industry with solid sterile injectible experience and backgroundand#149;Must have knowledge of secondary packaging and isolator experienceand#149;Aseptic experience is requiredand#149;Must have completed black or green belt trainingand#149;Must solid understanding and experience of freeze drying processand#149;Knowledge of industry standard practicesand#149;Must be a team player with interpersonal skills]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[GCP Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob980A22989ABD4A6B482579F5001FBA72</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/GCP-Auditor_1651658.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Job Requirements:and#60;/band#62;and#149;Must have 5 solid years of GCP auditing experience (both clinical site and vendor auditing) in a pharmaceutical or biotech companyand#149;BA/BS in science related field, requiredand#149;GLP auditing experience, preferredand#149;Experience writing SOPs and reports, requiredand#149;Excellent communication and writing skillsand#149;Experience handling document reviews, requiredand#149;Must strive in a fast paced environmentand#149;Must strive as a member of a multi/cross functional teamand#149;Experience in a start up exposure is a plusand#149;Must be an effective listener and be able to collectively gather informationand#60;band#62;Job Duties:and#60;/band#62;and#149;Act as the main point of contact for GCP compliance questions for the project teamand#149;Attend regular meetings related to GCP complianceand#149;Act as a day to day resource for the GCP function and#149;Promote GCP awareness within the companyand#149;Plan, schedule, organize, map out and conduct all auditsand#149;Up to 30% domestic/international travel may be required]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[GCP Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob904C9CB015DED7B1482579F5001FBA7F</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/GCP-Auditor_1651659.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Job Requirements:and#60;/band#62;and#149;Must have 5 solid years of GCP auditing experience (both clinical site and vendor auditing) in a pharmaceutical or biotech companyand#149;BA/BS in science related field, requiredand#149;GLP auditing experience, preferredand#149;Experience writing SOPs and reports, requiredand#149;Excellent communication and writing skillsand#149;Experience handling document reviews, requiredand#149;Must strive in a fast paced environmentand#149;Must strive as a member of a multi/cross functional teamand#149;Experience in a start up exposure is a plusand#149;Must be an effective listener and be able to collectively gather informationand#60;band#62;Job Duties:and#60;/band#62;and#149;Act as the main point of contact for GCP compliance questions for the project teamand#149;Attend regular meetings related to GCP complianceand#149;Act as a day to day resource for the GCP function and#149;Promote GCP awareness within the companyand#149;Plan, schedule, organize, map out and conduct all auditsand#149;Up to 30% domestic/international travel may be required]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical QPPV Consultant  £90,000  Hertfordshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob68C221C008BF8589482579F5001FBA8B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-QPPV-Consultant-and-amp-SHARP16390000-Hertfordshire_1651661.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a reputable CRO with a heavy focus on pharmacovigilance.As part of ongoing expansion, I am looking to find a medically qualified professional with excellent rounded experience within drug safety processes.Expertise in narrative writing are as standard, with a qualitative approach. Successful candidates will thrive in a client focused environment - meaning that confidence and concise communication are as important as the necessary qualifications.MUST: Have 3+ years EU Pharmacovigilance experienceResponsibilities will vary depending on the project at hand - but will include:-Review and Approval of safety reports-Risk Management Plans-PSURs, DSURs and QC of other aggregated reporting-Provision of medical expertise -Training colleaguesCriteria:and#149;Doctorate in medicineand#149;5 plus years of pharmacovigilance experience in a Pharmacovigilance Departmentand#149;Knowledge of EU pharmacovigilance regulations, including writing SOPsand#149;Proven ability to meet deadlinesand#149;Highly motivation and flexibilityand#149;Client-oriented, fluent in English with strong communication skills (oral and written)and#149;Able to work in a multicultural environmentand#149;Proactive and enthusiastic approach to team workingand#149;Knowledge of MS Office (Word, Excel, PowerPoint) essentialIf you feel you suit the above criteria - please email your updated CV to t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[LIMS Administrator]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F159EA2C842899E482579F5001FBA97</referencenumber>
<City><![CDATA[Washington]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/LIMS-Administrator_1651662.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Job Duties:and#60;/band#62;and#149;Implement a brand new LIMS system from the ground upand#149;Perform training, design reports and workflows and#149;Create manuals, SOPs and training documentationand#149;Troubleshoot system errors, design and run test configurations, implement solutions internally and#149;Maintain the LIMS configuration and develop and#149;Maintain LIMS documentation and quality and regulatory complianceand#60;band#62;Job Requirements:and#60;/band#62;and#149;BA/BS in Engineering or Chemistryand#149;5+ years experience in the pharmaceutical, biotech or medical device industryand#149;Experience with invitro diagnostics is a plusand#149;Computer systems validation experience is a plusand#149;Project management experience is essentialand#149;Must be able to strive in a small, fast paced working atmosphere]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Medical Information Adviser  £45,000 cir  NW London]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2118DEF1C054E57D482579F5001FBAA3</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Medical-Information-Adviser-and-amp-SHARP16345000-cir-NW-London_1651663.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a leading name within CNS/ Neurology. With a portfolio that expands to consumer healthcare and beauty products, this pharma is one of the more interesting from a medical information perspective.Looking for a Senior Medical Information Adviser, I would like to speak to those with an in-depth pharmacy background + 2 years or more within a pharmaceutical company. Copy approval and product ownership are heavily valued as well as evidence of a keen interest/ involvement in both the scientific and marketing aspects of previous work.If you feel that you fit the bill, please email me your updated CV. Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Information Administrator  £25,000  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBC8F14CB0B9FCA86482579F5001FBAB0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Information-Administrator-and-amp-SHARP16325000-South-East_1651664.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global specialist in unlicensed medicines. After a promotion within the team, there is a demand for someone to cover the administration and databasing responsibilities within a fast paced environment.Duties include:- Manage the process regarding obtaining document translations- Prepare ad hoc reports to facilitate the continuous improvement of the Medical Information function within the Idis business- Ensure the most recent approved product information is included in the product database- Manage the process regarding obtaining controlled drugs import licencesCandidates with a strong life sciences background are preferred... exposure to the medical information environment is also a bonus.If you are interested, please contact Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance Manager  £50,000  Maidenhead]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE46A3462F5B0CA2E482579F5001FBABC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Manager-and-amp-SHARP16350000-Maidenhead_1651665.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a top 10 pharma, and globally renowned for its employee satisfaction.With a view to bring on a new pharmacovigilance manager, I am looking for those with broad experience across the drug safety spectrum.Candidates MUST: - have 3+ years UK pharmacovigilance experience- be up to date with 2012 PV legislation- have trained/ mentored/ supervised within drug safetyResponsibilities:Deputy Affiliate Safety Representative- Writing SOPs- Oversight of compliance- Ensuring Timely submissions- Keeping GPV updated with PV legislation- Co-ordination of affiliate review and submission of PSURs- Monthly ICSR reconcilliationOversight of AEs (Adverse Events)Training and Mentoring PV staffSupporting Med Info team with relevant safety related findingsSupporting medical aspects of device and nutrition safety ----------------If you feel you can live up to the above criteria, please send a copy of your updated CV to Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead GCP Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1D78E2B05F7E2B19482579F5001FBAC9</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Lead-GCP-Auditor_1651666.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Lead GCP Auditorand#60;/band#62;The purpose of this position is to manage and lead GCP Audits to assure that all aspects of clinical trials conducted have been executed in compliance with applicable US FDA, ICH GCP Guidelines and other government and/or country specific regulations.This is a 6 month contract to permanent position.and#60;band#62;and60 - and80 per hour depending on experience.and#60;/band#62;and#149;Ensuring clinical trials are performed in accordance with applicable study protocols, and are in compliance with GCP and ICH guidelines. and#149;Conducting clinical document audits on Investigator Brochures, Clinical Protocols and Study Reports, Case Report Forms, Data Listings, and Informed Consents.and#149;Conduct Internal audits on the Trial Master Files.and#149;Conduct GCP compliance audits of Investigator sites and Vendor facilities in accordance with annual Audit Plans. and#149;Conduct internal department audits to ensure compliance with Department Guidelines and Procedures, and GCP and ICH guidelines. and#149;Provide guidance on existing and new GCP regulations to clinical teams.and#149;Represent the CQA department on the clinical department teams.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Manager  Leidinggevende functie  tot 82k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2B1DFE0F93C2923F482579F5001FBAD3</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-Manager-Leidinggevende-functie-tot-82k_1651667.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Voor and#233;and#233;n van mijn klanten in Noord-Holland ben ik met spoed op zoek naar een Senior Regulatory Affairs Manager. Het betreft een international georiand#235;nteerde farmaceutische organisatie waar een resultaatgerichte cultuur heerst. Dit betekent ook dat deze organisatie werknemers beloont die veel energie en ideeand#235;n investeren in deze organisatie. De functie betreft een global rol binnen een team waarin iedereen global verantwoordelijkheden heeft.De Senior Regulatory Affairs Manager gaat leiding geven aan een team van 3 Regulatory Affairs Managers. Daarnaast zal je in deze functie rapporteren aan de Head Regulatory Affairs globally. Naast het leidinggeven zal je je ook bezighouden met de registraties zelf en ervoor zorgen dat alle MAAand#146;s tijdig in orde zijn. Als Senior RA Manager ga je ook de strategie bepalen voor de commerciand#235;le producten. Vereisten:-Msc in Farmaceutische, Biologische of Biotechnologische richting. -Vloeiend Nederlands en Engels in woord en geschrift. -Minimaal 7 jaar Regulatory Affairs ervaring in Biotech en/of Farmaceutische industrie-Uitstekende communicatieve vaardigheden bij voorkeur in een global team-Proactief-AnalytischSalaris en Voorwaarden:-and#128; 57000 and#150; and#128; 82000 bruto per jaar, afhankelijk van ervaring-Bonus van maximaal 20% afhankelijk van bedrijf/individueel resultaat-LeaseautoReageren:Klinkt dit als een logische volgende stap in je carriere en voldoe je aan het profiel, upload dan nu je CV. Indien je vragen hebt, bel Robin Priems op +31 (0)20 522 15 77and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SAS Programmer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8EE417879B33EFBD482579F5001FBADF</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/SAS-Programmer_1651668.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing is currently recruiting for a leading biotechnology company located in South San Francisco who have a focus on oncology. As a Clinical SAS programmer III, your SAS skills with be first class. You will be involved in the manipulation of data to produce tables, listings and graphs and have advanced skills in program validation. An expert in output verification, with experience gained specifically from within the clinical research environment (full life-cycle) you should be advanced in data analysis and reporting skills and be able to hit the ground running .Key Responsibilities: Programming includes: (not limited to)and#149;The data manipulation, analysis and reporting of primarily clinical trial data. and#149; Specifically, analysis files creation; and#149; table/listing/graph generation; and#149; program validation and documentation; and output verification. Work is to be performed in a team environment, where team members may be distributed across locations and Suppliers.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Project Manager; Cleaning Validation  Los Angeles]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob00B05C001A3F2345482579F5001FBAEC</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/URGENT-Project-Manager-Cleaning-Validation-Los-Angeles_1651669.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Requirements:-7-10 years experience working in utlities ; cleaning validation-experience in Biotech Industry-Project Management experience- Water systems,  WFI; PW; Compressed Air, HVACThis is an extremely urgent offer that has been open for a month and needs to be filled. Please call or send your resume if you are interested.Keywords:  CLEANING VALIDATION, UTILITIES, BIOTECH, PW, WFI, PM, PROJECT MANAGER]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QP  6 Month Contract  Midlands]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob514BFC08AC14BF58482579F5001FBAF8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QP-6-Month-Contract-Midlands_1651670.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The ideal candidate will have worked at a other large pharma companies as a QP, as well as being a strong communicator and commercial acumen. The candidate will have over 10 years QP experience, experience of working with liquids and creams or ointments, and a chemistry/microbiology degree background would be extremely beneficial. This is an excellent opportunity to start work in the middle of May for an exciting and large organisation. There is also the strong possibility of a permanent role arising at the completion of the contract. If you are interested or know anyone who may be, please contact Hemish Ilangaratne on 020 7758 7322 immediately.  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Principal SAS Programmer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC1C3A3117DD70053482579F5001FBB04</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Contract-Principal-SAS-Programmer_1651671.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Responsibilities:and#149;Perform role of primary statistical programmer on all assigned studies, integrated summaries, and responses to requests from regulatory authorities.and#149;Perform role of validation programmer on all assigned studies, assigned integrated summaries, and responses to requests from regulatory authorities.and#149;Create data definition tables for all SDTM and derived data sets for all assigned studies and integrated summaries.and#149;Create data mappings, SDTM and derived data sets, and data definition tables for all assigned partner studies.and#149;Review statistical analysis plans for all assigned studies and integrated summaries and provides comments to study biostatistician.and#149;Review annotated case report forms and provides comments to study database administrator.and#149;Review edit check specifications and provide comments to study data manager.and#149;Provide technical expertise and consulting to Director of Statistical Programming.and#149;Support direct supervisor and Director of Statistical Programming.Requirements:and#149;Masters Degree in Statistics, Biostatistics, Epidemiology, or Computer Science, or equivalent.and#149;Eight (8) years experience performing statistical programming using SAS in a pharmaceutical setting, or equivalent.and#149;Must have advanced knowledge of SAS  programmingand#149;Experience with NDA submissions, ISS and ISE.and#149;Strong communication skills.Please send me an updated resumes ASAP and please forward this to a colleague if possible.Thanks and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Specialistenbezoeker Farma  Amsterdam en omgeving]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE795AC4C8568321D482579F5001FBB11</referencenumber>
<City><![CDATA[Amsterdam]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Specialistenbezoeker-Farma-Amsterdam-en-omgeving_1651672.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Account Manager Farmaand#60;/band#62;and#60;iand#62;Noord-Hollandand#60;/iand#62;Ben jij de zelfstandige account manager / Specialisten bezoeker die voor deze gevestigde organisatie een nieuwe Farma tak kan opbouwen voor Nederland? De organisatie bestaat al 150 jaar en is groot in met name medical devices. In hun specialisme benaderen ze sinds vorig jaar ook de Farma in NL met 4 product specialisten. De doelgroep zijn oogartsen. Een zelfstandige opstart / pioniersfunctie waarvoor wij een gedreven kandidaat zoeken met een gedegen achtergrond. Het team van 4 kenmerkt zich door hun open en transparante manier van communiceren en team work. Samen bouwen zij aan deze nieuwe tak. Tenminste 2 jaar sales ervaring in de Farma is dus echt nodig!and#60;band#62;Functie-eisen:and#60;/band#62; and#149; Minimaal afgeronde HBO opleiding is een must and#149; Minimaal 2 jaar ervaring als rayon manager in de pharma waarbij je specialisten bezocht. Je past bij deze werkgever wanneer je ambitieus bent, klantgericht, pro-actief, je mening durft te geven maar ook bereidt bent te luisteren naar anderen. Hiernaast ben je resultaatgedreven. and#60;band#62;Salaris en voorwaarden:and#60;/band#62;Een zelfstandige pioniersfunctie meet veel vrijheid bij een grote internationale organisatie met mooie producten en een sterke pijplijn.  Ze bieden afhankelijk van ervaring een goed jaarsalaris van ongeveer 3500bpm (37,5uur per week), 13e maand met daarnaast een sterke bonusregeling. Hiernaast bieden ze een auto, laptop, telefoon en vaste onkosten vergoeding Een mooi pakket!and#60;band#62;Interesse of meer weten?and#60;/band#62;Neem contact op met Jolien van Real Staffing: 020 - 522 15 77. En mail je cv in wordformat naar: nl.pharma.perm @ realstaffing.comand#60;band#62;Keywords:and#60;/band#62;Farma / opthalmologie / optometrie / oogartsen / oogarts / specialistenbezoeker / huisartsenbezoeker / verkoop / sales  / account managerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR ACCOUNT EXECUTIVE  LEADING AGENCY IN CHICAGO!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob59FE84121805593B482579F5001FBB1E</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/SENIOR-ACCOUNT-EXECUTIVE-LEADING-AGENCY-IN-CHICAGO_1651673.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SENIOR ACCOUNT EXECUTIVE - MEDICAL COMMUNICATION AGENCY - CHICAGOMy client, located in Chicago, is looking for a Senior Account Executive to join their rapidly growing team. They are offering a very competitive salary, a bonus incentive, and full coverage on Health Benefits.Further, the agency as a whole has doubled in size and revenue for the past 3  years (year over year). They diversify their accounts and therapeutic areas, which has been key to the success of the agency.ROLE REQUIREMENTS:+ Agency experience in a medical communication, pharma, or advertising agency + Key, day-to-day representative to the client+ Manages client feedback and disseminates to the internal team+ Liaises with strategic personnel to ensure the proper strategic brand imperatives are met beyond a tactic+ Remains accountable for deliverables sent to the client+ Manages execution of tactical plans+ Develops and manages budgets, timelines and proposals+ Develop agendas for client meetings+ Communicates timelines and tasks to various internal departmentsIf interested, upload resumes directly or call Brian Barranti on (212) 707-8499 for more information.SENIOR ACCOUNT EXECUTIVE - LEADING AGENCY IN CHICAGO!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Pharmacovigilance Physician  Top 10 Pharma  £100k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDBEB8AA8ACDD5FC2482579F5001FBB32</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lead-Pharmacovigilance-Physician-Top-10-Pharma-and-amp-SHARP163100k-_1651674.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I am currently working for a global top 10 pharma company on a Lead Pharmcovigilance Physician Role. UK Based - Full Time - and#163;100,000+ Must have 7 years industry experience with extensive medical background - preferring clinical experience also. Reporting to the Global Medical Lead Physician, this position will have line management responsibility to Physicians in the activities of AERs, serious, expedited and pregnancy related. Guidance on follow up, medical review of aggregated reporting and signal detection. You must display evidence of the ability to succeed within a global matrix environment as well as competency and experience in line management. If you feel you adhere to the above criteria and would like a career defining role, please get in contact ASAP. Please send an updated CV to register your interest - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Local SAS programmer Year contract Cambridge Senior profile.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob40D7A3B21F88448A482579F5001FBB3E</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Local-SAS-programmer-Year-contract-Cambridge-Senior-profile_1651675.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[There are two very interesting contract positions open for one of the leading Biotechnology company in the Cambridge area. You need to support the statistical programming activities in the production of the analysis datasets, tables, listings, figures, electronic submission components, and complex ad hoc analyses. As a individual you are responsible for: *monitoring and meeting assigned study and program milestones. *requesting resources as needed. *leading a small team of support statistical programmers to accomplish tasks and communicate issues to senior management as necessary. *provides input to policy, operations, and capability building in Statistical Programming and Operations. *He/She develops and implements standard programming practices while also ensuring that they are employed across studies and programs. I am looking for somebody with the following qualifications: - 5-10 years SAS Base programming, with 5-7 years using SAS STAT, GRAPH and MACRO -5-10 years relevant industry experience -5-10 years clinical trial experience -2 years clinical database experience -Excellent knowledge of drug development process -Knowledge of CDISC standards including SDTM and ADaM -Knowledge of drug submission requirements Education Bachelorand#146;s or Masters degree, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, IT. The role is local based. Hourly rate should be around 55-70 dollars an hour. If you are interested please let me know within a short notice and respond with your most recent resume.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Operations Manager  Lextington  Oncology Phase 2b3]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF2424C996BDF9119482579F5001FBB4B</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Operations-Manager-Lextington-Oncology-Phase-2b-3_1651676.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Biopharma company based in the area of  Lexington Massachusetts is currently searching for a Director / Senior Director of Clinical Operations.Working on leading edge Oncology trials your role will be key in the managing of whole Clinical programmes patient recruitment strategy, for Phase 2b/3 Oncology small molecule clinical trials. Responsibilities:Manage activities and support ongoing clinical trial programs.Develop and maintain relationships with clinical investigators, opinion leaders and site personnel.Collaborate effectively with internal departments on study advancements.Oversee the safe and ethical conduct of the assigned programs.Collaborate with discovery, research, translational, and commercial groupWork with the core team to support and maintain clinical development plan and accompanying regulatory and commercial strategies.Qualifications: A M.D. or M.D. /Ph.D. degree in a relevant scientific discipline with a minimum 2-4 yearsand#146; experience in Oncology clinical research in the biotech/pharmaceutical industry.Board certification in Oncology required. Broad understanding of clinical trials processes with experience in oncology therapeutic agentsand#146; development a strong plus.Decisive and proactive, hands-on, roll-up-the-sleeves style and attitude.Exceptional analytical ability and a creative, solution-oriented style.Flexible and able to work in a fast-paced, rapidly changing environment.Team-oriented with strong interpersonal skills and ability to collaborate effectively with other groups.Hard-working, energetic and passionate about making a difference.Highest integrity; committed to ethics and scientific standards.Willing and able to travel domestically and internationally, minimum 30% of time.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SAS programmer  Lexingtom, Massachusetts  CDISC & ISSEISE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob40F6F1843709A27B482579F5001FBB57</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/SAS-programmer-Lexingtom-Massachusetts-CDISC-and-amp-SHARP38-ISSE-ISE_1651677.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A senior SAS programmer is required by a leading Oncology Biopharma based in the area of Lexington. Working as part of the technical team supporting the Biostatistics team your role will be key to early phase clinical trials to CDISC standards Responsibilities:and#149; Provide general SAS programming support to Clinical Research and Development.and#149; Work closely with statisticians to generate analysis data sets and create tables, listings and graphs for interim analyses, preliminary reports and Clinical Study Reports for in-house use, publications, and/or regulatory submissions.and#149; Perform quality control checks on program code and outputs produced by other team members.and#149; Conduct data edit checks to ensure the quality of source data.and#149; Develop Analysis Plans/Mock Data Presentationsand#149; Enhance existing utility programs and develop new utility macros to standardize data processing and output procedure. and#149; Review and provide input on programming related documentation including plans and specifications.and#149; Respond to project-level request for clarification of analyses from regulatory agenciesand#149; Manage programming timelines, schedules, and activities on specific programming tasks.Qualifications:and#149;Bachelorand#146;s degree in life science, statistics, mathematics, computer science, or related field required; Masterand#146;s degree preferred. and#149;5+ years of SAS programming experience in biotech or pharmaceutical industry preferably with oncology experience.. and#149;Experience in SAS programming language, macros, and procedures. and#149;Working knowledge of ISS/ISE, CDISC standards (SDTM, ADaM). and#149;Detail oriented with strong organizational and communication skills. and#149;Ability to work in a team environment. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Principal Biostatistician  Early Phase Oncology Trials]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC3F15E63AE5E9432482579F5001FBB64</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Principal-Biostatistician-Early-Phase-Oncology-Trials_1651678.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Position Senior / Principal Level BiostatisticianTherapeutic area - Oncology (early phase)Location - Greater BostonCompany size - approx 150 - 200Company profile:A Biopharmaceutical company focused on the discovery and development of transformational medicines for complex disease, with an initial focus on cancer.  With 5 compounds in oncology clinical trials and a strong pipeline that is expected to produce several more clinical development candidates in the near future this company are an exciting environment for Biostatisticians with early phase oncology experience who are looking to be part of a growing leading edge organisation who will be making a positive difference to the treatment of future cancer patientsThe Senior  / Principal Biostatistician will be working with a cross functional program team as the statistical lead, responsible for statistical activities across multiple studies, and reporting to the program medical director. The ideal candidate is a good communicator, high-energy, self-motivated, and forward thinking. Experience working in oncology development is preferred, but not required. Requirements:PhD (MS) in statistics or related discipline with at least 5 (7) years of experience in the pharmaceutical or biotech industry Demonstrated ability to effectively contribute to the statistical aspects of clinical protocol design, data interpretation, review and reporting of results for multiple studies and projects Practical experience with application of advanced statistical methodologies to clinical trial design/analysis and with regulatory reporting/submissions Ability to communicate statistical concepts in a clear and concise manner Excellent verbal, writing, and presentation skills.Experience managing outsourced biostatistical services Proficiency with statistical software tools such as SAS, S-Plus, R, EAST Familiarity with regulatory requirements and considerations (e.g. GCP, ICH, 21CFRpart11, CDISC) Positive interpersonal work habits and communication skillsand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ALLROUND Quality Assurance Manager  for medical device company  NL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob58778D0351F1D9A5482579F5001FBB70</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ALLROUND-Quality-Assurance-Manager-and-amp-SHARP150-for-medical-device-company-and-amp-SHARP150-NL_1651679.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[ALLROUND Quality Assurance Manager and#150; for medical device company and#150; The NetherlandsAs QA/RA manager you will be responsible in this freelance position for:QA/ RA compliance:and#149;Supervise QA strategy; generate new strategy and plans on improving product qualityand#149;Implementing and maintaining Quality Management System in accordance to ISO13485 and CEand#149;Obtaining regulatory approval for Europe and US.We are looking for:and#149;Freelance QA/RA Manager with experience 5- 8years in medical device industryand#149;Preferably worked in/ experience in start-up companyand#149;Experienced with class 2a-2b productsDuration of the project is 5 -6months.Hourly rate: needs to be discussed. Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[MSL Oncology SouthWest]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6326CAD51066B67E482579F5001FBB7D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/MSL-Oncology-South-West_1651680.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Liaising with internal and external stakeholders to exchange scientific data relating to the Oncology/ Haematology field-Responding to off-label requests from clinicians-Working on medical education activities at regional level-Staying up-to-date with all relevant clinical data/ publicationsIf this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Medical Affairs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5AA56E9A3D1B9CD6482579F5001FBB8A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Head-of-Medical-Affairs_1651681.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Lead the Medical Affairs team and influence strategic decisions -Establish and develop clinical and academic KOL relationships and lead advisory boards-HCP education: lead education providers in company products-Develop brand team messages-Internal training/ communication with Marketing, Medical Fieldforce, External and#38; Public Affairs, Quality and#38; Regulatory Affairs-Rand#38;D: stay up to date with all clinical evidence for the companyand#146;s superior portfolio-Liaise with medical field force, marketing and external affairs to define strategic objectives and opportunities If this role interests you please email me.nutrition, dietitian, medical affairs, KOL management, nutrition, dietitian, medical affairs, KOL management, nutrition, dietitian, medical affairs, KOL management, nutrition, dietitian, medical affairs, KOL management, nutrition, dietitian, medical affairs, KOL management, nutrition, dietitian, medical affairs, KOL management,  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Science Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC679A3007DA32BC6482579F5001FBB97</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Science-Manager_1651682.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilitiesand#149;The person who fills this role will be expected to maintain and develop relationships with KOLs, participate in coordinating and conducting peer-to-peer interactions and medical presentations, and serve as a reviewer for independent research initiatives and publications. and#149;They will represent Medical Affairs at national and international meetings, congresses and symposiums. Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice and reviewing submissions and formulary applications will all be part of the role. and#149;The MSM will also be expected to work with cross-functional colleagues in sales, marketing, market research, training, health economics, clinical operations and external affairs. and#149;They will build solid and credible relationships with the medical community on the companyand#146;s behalf and cultivate key thought leaders and product advocates in the Academic and Community settings. If this role interests you please contact Orna Mc Donald on 02077587311 or email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Scientific Affairs Manager Diabetes]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB90B4433EF8CCDE482579F5001FBBA1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Scientific-Affairs-Manager-Diabetes_1651683.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Assessing research articles and reports related to company products and potential future product development. -Rating opportunities for Investigator Initiated Trials -Building credible KOL relationships-Represent the company to world leaders in Diabetes care and research-Understanding regulatory compliance and FDA requirements for the Medical Device industry as they relate to the companyand#146;s products-Providing information and recommendations to Rand#38;D and other departments to monitor reactions related to the companyand#146;s Diabetes products-Coordinating regional education and scientific symposia-Ensuring advocacy, clinical knowledge, and proper training on company products with KOLs and academic centers.-Understanding the difference between making recommendations in therapy based on validated standards of clinical affairsIf this role interests you please email me.Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Devlopment Quality Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD2A1B4BA095E58C0482579F5001FBBAE</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Devlopment-Quality-Associate_1651684.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Were seeking an experienced Development Quality Associate to join a well known global Generic Pharmaceutical company. This contract position is for highly experienced individual  looking to join a fast-paced team. and#60;band#62;This role will involve: and#60;/band#62;- GPvP oversight of Patient Orientated Programmes (POP) as per global requirements. - Ensure that POP vendor assessment is conducted as per global process. -Follow-up and review CAPAs developed for POP vendors and maintain list of qualified vendors. - Conduct proactive in-process quality and compliance review through monitoring of adequate Key Quality Indicators (KQIs) and assure that gaps are addressed. - Maintaining Quality System in accordance with the CPO Quality Plan. -Assist global pharma Devleopment QA to support the preparation, execution and follow-up of audits on PV activities. - Provide support HA inspections of the CPO or external service providers. - Review responses to local Health Authorities and ensure responses have been sub-mitted and met relevant CAPAs and have been completed and closed. - Ensure conduct of adequate training at the CPO for all GPvP activities by defining, planning and supporting training activities. and#60;band#62;To be eligable for this role you must: and#60;/band#62;- Have a degree in Life Sciences or related fields. - Minimum of 5 years experience in the pharmaceutical industry in a relevant field such as pharmacovigiliance, clinical development or a directly related area.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QA Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC4A3C8E60595D7D9482579F5001FBBBB</referencenumber>
<City><![CDATA[Melbourne]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/QA-Associate_1651685.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Were seeking an experienced Development Quality Assurance Associate to join a well known global Pharmaceutical company. This contract position is for highly experienced individual  looking to join a fast-paced team. and#60;band#62;This job will involve: and#60;/band#62;- To manage the duty of care batch release process, meeting all regulatory standards. - Manage customer complaints - Assist in implementing and improving quality management systems. - Perform duty of care release actvities for all stock. - Ensure all quality issues associated with release activities are investigated and documented according to approved procedures. - Manage logging, storage and destruction of retention samples in compliance with local erquirements and regulations. - OTC GMS within Australia/New Zealand. and#60;band#62;To be eligible for this job you must: and#60;/band#62;-Qualifications in Chemistry, Pharmacy, Biology, or related Science or discipline. -Knowledge of GMP requirements and quality systems associated with pharmaceutical production. - Experience in Quality Assurance, Quality Control or R and#38; D. - Be computer literate (Microsoft Office) with skills in the use of work proessing, spreadsheets, databases and information and management systems.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Laboratory Analyst]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob53899D0F1969F933482579F5001FBBC9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Laboratory-Analyst_1651686.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An excellent company they have a multitude of sites in the UK and are market leading in service with the highest level of audited standards in the industry. Due to continued expansion we are now looking to recruit a Senior Analyst.Responsibilities include:-Reviewing analytical data.-Production and validation of standard and control material.-Participation in development and validation of new assays.-Maintenance of equipment.-Maintaining competence in analytical procedures to provide continuity of service in times of staff shortages.If you are interested you must have:-Excellent communication and organisational skills and ability to work to deadlines.-Scientific background - educated to Degree level in one of the Biosciences -Experience with Analytical Techniques Including specifically Immunoassay and Chromatographic procedures including GCMS and LCMSThey are looking to offer an excellent salary and benefits scheme if you are interested please send an updated CV to John Morkus for further details.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB7F68F994E0DE657482579F5001FBBD6</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Regulatory-Affairs-Consultant_1651687.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Due to an exciting product pipeline and a subsequent growth within their Regulatory Affairs team, my client is seeking a Senior Regulatory Affairs Consultant for a 12 month contract based in Sydney. This role will support regulatory objectives, advice, and strategy in alignment with department and corporate goals, coordinate regulatory document preparation for regulatory submissions and keep updated of evolving regulatory procedures and practices.Role responsibilities:1.Coordinates, prepares, and reviews all appropriate regulatory submissions for TGA submissions within a specified time frame in conjunction with the organization2.Evaluates changes to regulatory documents and formulates strategies for correct filing categories, with guidance from supervisor3.Interacts effectively with functional business units in order to coordinate and facilitate documentation required for submissions, ensuring that departmental timelines are met4.Coaches and mentors other associates.  Trains less senior associates to review change requests and provides guidance to other associates in the preparation of other TGA submissions5.Interacts with TGA and all company sites via written and phone communications6.Reviews and analyzes regulatory and related publications to assure compliance and anticipate future regulatory actionThis role will be a 12 month contract position. For more information please contact Gemma Macpherson on 02 8251 1100.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of International Relations]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6220A67663268F7E482579F5001FBBE2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Director-of-International-Relations_1651688.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The role will entail working within the Western Europe International Public Affairs team, to support the public affairs strategies and programmes for the Pain/CNS/ Alzheimers portfolio. Duties will include: Delivering the pain portfolio policy strategy as part of a cross functional team: - Provide guidance on development of pain policy strategy and tactics - Ensure all strategy and tactics deliver against cross brand/ cluster objectives and incorporate broader corporate opportunities - Active participation in delivery of pain policy plan to countries and garner support for roll out of activity including: - Achieve ambassadorship by senior business leaders for PAP colleague delivery against pain policy plan The right candidate will ideally have experience in the pharmaceutical industry. If interested please do let me know and send me an updated CV or call 0207 758 7322 and ask for Mary Kay and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Parttime Health Economist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob015971F498EEA913482579F5001FBBEF</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Part-time-Health-Economist_1651689.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, one of the worlds largest Pharmaceutical companies, is searching for a Health Economist for a part-time/flexible working arrangement contract based in Sydney. Purpose:- To plan and#38; prepare high quality applications for reimbursement to the Pharmaceutical Benefits Advisory Committee (PBAC)- To plan and#38; prepare high quality applications, in collaboration with the Pricing Associate,  to the Pharmaceutical Benefits Pricing Authority (PBPA)- To collaborate with cross-functional colleagues to develop, communicate and execute risk sharing agreements with the Department of Health- To provide advice to internal customers on local reimbursement and#38; pricing strategies as required.- The role will have responsibility across PBAC submissions and have full end to end ownership, consequently dealing with all areas of the submissionRequirements:- Relevant qualifications or a tertiary degree in Pharmacy, Economics, Medicine or Health Sciences; - Experience in pharmaco-economics or health economics within the Australian, Canadian or UK pharmaceutical industry, or with a large evidence based related health care sector (Government or academia), or in consulting; - PBAC submissions experience- Excellent communication skills This role offer a part time working option or flexible working arrangements. Apply now or for more information contact Gemma Macpherson on 02 8251 1100.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Health Economist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC64C29E399DD0107482579F5001FBBFB</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Health-Economist_1651690.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, one of the worlds largest Pharmaceutical companies, is searching for a Health Economist for a part-time/flexible working arrangement long-term contract based in Sydney. Purpose:- To plan and#38; prepare high quality applications for reimbursement to the Pharmaceutical Benefits Advisory Committee (PBAC)- To plan and#38; prepare high quality applications, in collaboration with the Pricing Associate,  to the Pharmaceutical Benefits Pricing Authority (PBPA)- To collaborate with cross-functional colleagues to develop, communicate and execute risk sharing agreements with the Department of Health- To provide advice to internal customers on local reimbursement and#38; pricing strategies as required.- The role will have responsibility across PBAC submissions and have full end to end ownership, consequently dealing with all areas of the submissionRequirements:- Relevant qualifications or a tertiary degree in Pharmacy, Economics, Medicine or Health Sciences; - Experience in pharmaco-economics or health economics within the Australian, Canadian or UK pharmaceutical industry, or with a large evidence based related health care sector (Government or academia), or in consulting; - PBAC submissions experience- Excellent communication skills This role can offer a part time working option or flexible working arrangements if required. Apply now or for more information contact Gemma Macpherson on 02 8251 1100.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Projectapotheker voor bereidingsapotheek gezocht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob511E221321017468482579F5001FBC07</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Projectapotheker-voor-bereidingsapotheek-gezocht_1651691.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een bereidingsapotheek die farmaceutische zorg levert in de regio noord-Limburg is op zoek naar een project apotheker ter versterking van hun team.Het bedrijf is ISO 9001 gecertificeerd (GMP) en levert aan meerdere instanties farmaceutische zorg zoals psychiatrie, ziekenhuizen en verslavingszorg.Het team waarin je komt te werken bestaat uit 5 ziekenhuisapothekers, drie openbare apothekers en een projectapotheker.Bij een van de klanten van de organisatie wordt een EVS (elektronisch voorschrijf systeem) geand#239;mplementeerd waarvoor men momenteel ruimte heeft voor een enthousiaste apotheker. Herken je jezelf in dit profiel en wil je deze uitdaging aangaan dan is dit de job voor jou!Functie inhoud:Als projectapotheker coand#246;rdineer je de implementatie van het EVS en voer je deze uit. Aandachtspunten hierin zijn de implementatie van het systeem op de polikliniek en kliniek, de herinrichting van de klinische geneesmiddelendistributie en tevens de uitwisseling van gegevens met openbare apotheken en het systeem van onze bereidingsapotheek. Naast dit project zit je met andere apothekers in klantenteams om het relatiebeheer met externe klanten te onderhouden.  Secundaire voorwaarden:- Marktconform salaris van maximaal and#128;55000 afhankelijk van je ervaring- Goede secundaire voorwaarden zoals pensioen, reiskostenvergoeding en vakantiedagenFunctie eisen:- MSc Farmacie, en apothekersdiploma- Ervaring met farmacotherapie en farmaceutische dienstverlening- Kennis van GMP en GMPz- Nederlands en Engels: vloeiend in woord en geschriftBen je geand#239;nteresseerd in deze functie en wil je meer informatie? Druk dan op de and#145;applyand#146; button en upload je cv ter attentie van Gwen Reniers.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE6ABC6476277FC7C482579F5001FBC13</referencenumber>
<City><![CDATA[Melbourne]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Regulatory-Affairs-Associate_1651692.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client based in Melbourne, has two openings within their Regulatory Affairs department and is currently looking for an Associate AND a Senior Associate for permanent positions. The roles will focus on providing support for regulatory submissions, successfully completing regulatory projects and enabling the timely launch of new products. The roles will also provide scientific, medical and regulatory expertise to the company. Responsibilities: - Perform activities required to obtain and maintain approvals in markets for the company and licensees/partners - Prepare standard documents for new registrations and variations - Prepare submission dossiers- Prepare responses and reports for the Health Authority- Assist in developing Product Information, Consumer Medicine Information, labels and other documentation- Prepare and submit pricing applications - Submit Safety Related Notifications and Product Information (or equivalent) updates to relevant Health Authorities - Assist in developing draft artwork and liaise with third parties to enable the production of labels, cartons and foils Requirements: - A tertiary health or science qualification (Science, Pharmacy and Medicine) - Minimum 2-3 years regulatory affairs experience- Experience with submission through the new TGA streamlined submission process - Prescription medicine experience If you are interested in this opportunity please APPLY NOW or contact Gemma Macpherson on 02 8251 1100.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Regulatory Affairs Consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7CAC5BA7BDBA43A7482579F5001FBC1F</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Contract-Regulatory-Affairs-Consultant_1651693.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My global client is a leader in research based pharmaceuticals and is looking for a Senior Regulatory Affairs Associate for a 12 month contract based in Sydney. This role is an exciting opportunity to work on a broad range of therapeutic areas from general medicines, specialty medicines, womens health and diagnostic imaging. Role responsibilities: - To ensure that all NCEs, new indications and new presentations are registered in the best possible time fram and with the best possible labels - To ensure that all company products remain compliant with all relevant regulatory and corporate requirements throughout their product lifecycle - To partner with relevant stakeholders within the company to assist in achieving optimal company outcomes - Registration of new products, indications and presentations - Maintenance of existing products - Internal stakeholder support - External stakeholder relationships Role requirements: - Tertiary qualifications in Science of Pharmacy - 4-7 years of regulatory experience, working with prescription medicines - Working knowledge of Australian and New Zealand regulatory requirements - Ability to work unsupervised with demonstrated time management skills - Project Management skills - Experience with the new TGA processes This role requires someone who is highly autonomous and can work independently and with high quality. This opportunity will offer flexible working arrangements to the successful candidate.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Statistician  Midlands  up to £35K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobADD48F5033ACB98E482579F5001FBC2B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Statistician-Midlands-up-to-and-amp-SHARP16335K_1658670.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An exciting opportunity has arisen within a established medium sized contract research organisation who are in the process of strengthening there technical statistical department.   Based in the Midlands the organisation are seeking to appoint a talented statistician who will be required assist with the statistical analysis and reporting of Clinical Trials.The successful candidate will report in to the director of Biostatistics and would be required to perform programming, validation and production of regular statistical summaries of ongoing trials. The ideal candidate must be computer literate, educated to degree level in mathematics, statistics or another subject with a strong statistical component and posses at least two years of experience using statistics in a clinical research environment, including SAS programming experience. On offer is a salary of up to and#163;35,000 dependant on experience and the chance to develop your career within a stimulating environment while working for a specialised forward thinking organisation. For more information please contact Immanuel Ross at Real Staffing on 0207 758 7311]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Gruppenleiter Software bis 70.000 EUR Hamburg]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAB66D6F4DBBDB102482579F5001FBC3B</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Gruppenleiter-Software-bis-70000-EUR-Hamburg_1658671.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde sucht fand#252;r die Festanstellung einen Gruppenleiter Software. Das Unternehmen ist im Raum Hamburg ansand#228;ssig.Gruppenleiter SoftwareAnforderungen:Studium (technische) Informatik, Elektrotechnik, Nachrichtentechnik o.and#228;.Einige Berufserfahrung in C#, .NET und C++ sowie Embedded Software sollten vorhanden sein. Fundierte Erfahrungswerte in verschiedene Betriebssysteme wie, Windows Embedded und RTOS sind unerland#228;sslich. Des Weiteren Konnten Sie bereits langjand#228;hrig Erfahrung in UML-Tools sammeln. Darand#252;ber hinaus bringen Sie Expertenkenntnisse in ARM Mikrokontroller. Wesentlich von Vorteil sind Erfahrungen in IEC 62304 und Erfahrung in Fand#252;hrung und Motivation von Mitarbeitern.Aufgaben:Sie sind verantwortlich fand#252;r Entwicklungsprojekte sowie der Teams. Sie Reviewn und Steuern Arbeitsaufgaben. Sie sind fand#252;r die Erstellung von Softwarepflichtenheften sowie Softwarearchitekturen zustand#228;ndig.  Sie evaluieren und wand#228;hlen entsprechende Entwicklungstools aus. Des Weiteren sind Sie fand#252;r die Betreuung von externen Entwicklungspartnern verantworltichSie Wollen eine spannende Tand#228;tigkeit als Gruppenleiter Software? Sie interessieren sich fand#252;r Signalverabeitung, verteilte Systeme?Dann bewerben Sie sich jetzt als Gruppenleiter SoftwareSenden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Senior Quality Engineer  San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1EAC0520581FCBD4482579F5001FBC47</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/URGENT-Senior-Quality-Engineer-San-Diego_1658672.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has an urgent need for a Senior Quality Engineer who specializes in design control, and can do documentation review. The position will entail design history files and documentation.good communication is a must to be able to deal with cross functional teams.Please send your resume immediately if you believe you would be a good fit.McElla]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Medical Device  Michigan  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2E58F3088EE5CC0C482579F5001FBC56</referencenumber>
<City><![CDATA[Michigan]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Medical-Device-Michigan-Contract_1658673.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An international medical device manufacturer is seeking a skilled professional to fill the role of Quality Engineer.  The company, located in Michigan, aims to provide high quality medical devices to ensure patient care and increase efficiency amongst healthcare professionals.  As annual revenue continues to grow year over year the company prides itself in hiring qualified individuals who exceed expectations and aim to develop their skills.  The Quality Engineer position will be a prominent factor in continued growth and employee development.The Quality Engineer is responsible for supporting new product development, vender evaluation, qualification, and performance, and insuring all products adhere to regulatory agency and FDA standards.  The Quality Engineer will perform quality management on product development teams, ensure the quality and reliability of current test methods, and ensure documentation and SOPs are updated and implemented.  Additionally, the Quality Engineer will perform internal audits and report findings to upper level management.  The Quality Engineer is responsible for developing new vendor relationships and evaluating current vendors performance.Qualifications:- B.S. in Engineering or equivalent degree- 5+ years experience in the medical device industry- Strong understating of FDA regulations- Excellent managerial skills- Strong communication skillsIf you are interested in this position please apply now or call 312-453-9088 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Softwareentwicklungsleiter 50.00075.000 EUR Hessen Festanstellung]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEA0C8365293C5F33482579F5001FBC64</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Softwareentwicklungsleiter-50000-75000-EUR-Hessen-Festanstellung_1658674.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Die Real Staffing Group ist eine spezialisierte Personalberatungsagentur fand#252;r die Pharma- und Medizintechnikindustrie. Wir sind Experten im Bereich der Besetzung von Fach- und Fand#252;hrungskrand#228;ften. Mein Kunde sucht fand#252;r die Festanstellung einen Softwareentwicklungsleiter. Das Unternehmen ist im Rhein-Maingebiet ansand#228;ssig.SoftwareentwicklungsleiterAnforderungen:Sie entwickeln anhand von CAD/CAM neue Software fand#252;r die Medizintechnik. Sie sind fand#252;r die Leitung der Projekte zustand#228;ndig und arbeiten Abteilungsand#252;bergreifen. Sie optimieren beispielsweise Prand#252;fverfahren fand#252;r das QM und sind somit fand#252;r die Qualitand#228;tssicherung mit verantwortlich. Sie sind ebenfalls fand#252;r die Kommunikantion mit den Kunden verantwortlich.Profil:Studium der (technischen) Informatik, Elektrotechnik o.and#228;.Mehrere Jahre Berufserfahrung in der Entwicklung bzw. LeitungFundierte Kenntnisse in C#, WPF und C++.Erfahrung mit Visual Studio und/oder 3D-BildgebungSehr gutes Deutsch ist notwendigSie wollten schon immer Verantwortung and#252;bernehmen? Sie wollen in einem international und sicheren Unternehmen arbeiten? Dann bewerben Sie sich jetzt als SoftwareentwicklungsleiterSenden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lab Technologist  Brussels Region  MT(ASCP) DutchFrench or English]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob49E21DCB243BA740482579F5001FBC6E</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Lab-Technologist-Brussels-Region-MTASCP-Dutch-French-or-English_1658675.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[For one of my business partners located in the and#60;band#62;Brussels regionand#60;/band#62;, i am looking for a and#60;band#62;Laboratory Technicianand#60;/band#62;. Are you interested or do you know someone who does, please let me know! It is an excellent chance to fastrack your career within an international team of professionals! and#60;band#62;Requirementsand#60;/band#62;: and#149;and#60;band#62;Bachelors degree and#60;/band#62;or equivalent in a science related discipline required and/or and#149;and#60;band#62;MT(ASCP) certification and#60;/band#62;or equivalent certification and#149;Experience as a Medical Technologist in a and#60;band#62;clinical laboratoryand#60;/band#62; and#149;Or an equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. and#60;band#62;Responsibilitiesand#60;/band#62;: and#149;Responsible for the day to day operations of the and#60;band#62;laboratory unitand#60;/band#62;. and#149;Organises daily work activities within the laboratory unit to ensure efficient and effective scientific and administrative operations and#149;Trains Medical Technologists and and#60;band#62;Laboratory Assistants and#60;/band#62;in the unit and assesses performance. and#149;Oversees and reviews daily area and#60;band#62;Quality Control and#60;/band#62;and maintaining the and#60;band#62;QC databaseand#60;/band#62;. and#149;Sets up and validates new assays as assigned.  and#60;band#62;Salary and Benefitsand#60;/band#62; and#149; Market competitive salary and#149; and#60;band#62;Bonusand#60;/band#62; and#149; 13th Month and#149; and#60;band#62;Hospitalisationand#60;/band#62; and#149; Meal Vouchers and#149; Indefinitely contract and#149; Transportation cost and#149; Among others and#60;band#62;Interested? and#60;/band#62;You can reply to this e-mail or call and#60;band#62;Jonathan Gonzalez and#60;/band#62;on  and#60;band#62;+31 20 522 1577and#60;/band#62;, send me also your newest CV. Are you for something else? please let me also know. j.gonzalez @ realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Biostatistiker  Biostatistician  NRW  12 months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob81D1C5F8C722B970482579F5001FBC7B</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-Biostatistiker-Biostatistician-NRW-12-months_1658676.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Ihre Aufgaben: - Proaktive Beteiligung in allen Aufgabenbereichen mit statistischem Schwerpunkt, wie z.B. geeignete statistische Studiendesigns und statistische Auswertungen - Entwicklung und Review von Studiendokumenten sowie Review von Zulassung- und sonstigen Behand#246;rdendossiers - Begutachtung von Studienergebnissen und medizinischer Fachliteratur sowie der verwendeten Methodik hinsichtlich biometrischer Sachverhalte - Analyse, Aufbereitung und Darstellung klinischer Studienergebnisse sowie von Daten aus unterschiedlichen Quellen fand#252;r Dossiers zur Nutzenbewertung von Arzneimitteln - Anwendung und Entwicklung biometrischer Methoden, Begutachtung, Bewertung und Umsetzung von methodischen Vorschland#228;gen zur Analyse von Ergebnissen -  Stand#228;rkung der allgemeinen biometrischen Kompetenz, statistische Weiterentwicklung  Ihr Profil:- Mindestens 5 Jahre Berufserfahrung im Bereich der Statistik erwand#252;nscht Breites Fachwissen von statistische Methoden in der Medizin und (Grund-) Verstand#228;ndnis von medizinischen Zusammenhand#228;ngen  - Engagiert, teamfand#228;hig, flexibel, Verhandlungskompetenz (Interaktion mit internen und externen Partnern)  - Analytisches und konzeptionelles Denken und ein groand#223;es methodisches Interesse  - Sicherer Umgang mit relevanter Statistik-Software  - Sichere Deutsch- und Englischkenntnisse in Wort und Schrift, sowie sicherer Umgang mit MS Office und modernen Informationsmedien Standort: NRWDauer: 12 months + (extension possible)Rate: NegotiableStart: June/Juli 2012If you are interested in this position please contact Vincent Klauser at Real Pharma on + 49 (0) 69 264 898 400 or email v.klauser(at)realstaffing.com for more information.As a specialist recruiter in Data Management and Biostatistics positions for Pharmaceutical clients in Germany and Austria, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Copywriter  New York City]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob62C7C802C449683A482579F5001FBC87</referencenumber>
<City><![CDATA[New York]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Copywriter-New-York-City_1658677.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Senior level Copywriter required to join a forward thinking New York City based Medical Communications agency. RESPONSIBILITIES -Execute Brand Focused creative concepts that are on strategy across all media. -Must be able to handle more high-level projects as well as several assignments at a time. -Generate breakthrough ideas and constantly strive for new, better, more innovative solutions. -Adapt brands to digital, DM and Broadcast environments. -Show understanding of clientsand#146; marketing needs and consumer attitudes. -Manage workflow efficiently and take responsibility for timing and delivery.  -Read mechanicals and perform other pre-production tasks related to their projects. -Stay current with changes in technology and demonstrate technical competence.  SKILLS and#38; EXPERIENCE -4-10 years experience. -Demonstrated BRAND work. -Must have a strong portfolio of produced work. -Must demonstrate experience in Digital, DM, Print, interactive, TV and Radio production with a BRAND Focus. -Demonstrated experience in Oncology or Diabetes is a bonus  -Bachelorand#146;s degree required This is an excellent opportunity to join a growing, stable organization that is going to offer a great working environment. This is an on-site position and candidates will have to be able to commute to New York, New York. Salary is commensurate with experience and75K-and100K. If you are interested please upload your resume or Christian williams on 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Chinese speaking GCQA Specialist Quality Manual and Global SOPs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2355036B6228AE56482579F5001FBC92</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Chinese-speaking-GCQA-Specialist-Quality-Manual-and-Global-SOPs_1658678.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[For a pharmaceutical company based in Amsterdam the Netherlands Im looking for a QA professional with a profound command of the Chinese language. The company is currently exploring exciting new business opportunities in China, further expanding the Global Clinical Development of the company. Are you up for a challenge and do you want to work in a fast paced, international environment? Then we are looking for you!Job responsibilities: - Support the companies quality manual implementation and Global Clinical Development with a focus on China, including reviewing local SOPs and ensuring compliance with ICH/GCP, the companies standards in the area of GCP an PV- Control quality documents like SOPs, Forms and templates- Support Change Management through Document Control System which includes:- Notifying staff of new or revised controlled documents- Contact for the technical questions relating to the use of the document control system- Maintain data sheet linked with document control system of current valid SOPs as well as overviews on SOP related documents- Maintain electronic SOP history- Participation in the system and SOP related working and discussion groups- Contributing to the regular reviews and revisions of SOPs- Tracking the workflow status and providing updates- Support and work closely with all areas of CQA in the achievement of the missions and objectives of the department  Secondary benefits:- Competitive salary of maximum and#128;50000- Average bonus (upon request), good pension and other benefitsJob requirements:- MSc / BSc in life science / comparable- Minimum of 2 year experience working with quality systems in the pharmaceutical industry- GMP is required, additional GCP knowledge is preferred- English: fluent both spoken and written - Good command of Chinese language (the ideal candidate can read, speak and write Mandarin)Are you enthusiastic and do you want to learn more about this vacancy? Press the apply button and upload your cv for Gwen Reniersand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SAS Programmer Contract CRO]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob30A77569CD9BF673482579F5001FBC9F</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SAS-Programmer-Contract-CRO_1658679.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities/Responsibilities:You will serve as a programmer on selected multiple projects and support the lead statistician or lead programmer on projects. This will be done by providing statistical programming support for database extractions, data mapping, data summaries and listings, and validation programming support in the production of statistical appendices.You will manage your own time spent on projects; ensuring deadlines are accomplished, with the delivery of high quality work while remaining on budget.Where applicable you will provide the Biostatistics Project Manager, or project leads, with timely, accurate status reports, interact and communicate with other team members as needed with the project team. Ensuring projects are well documented and consistent with company SOPs and working procedures is standard.Experience:For consideration you will have good and relevant proven industry and SAS programming experience in a clinical trial environment. A good understanding of database structures and working with complex data structures.Have a proven ability to work independently or within a team along with experience working to Statistical Analysis Plans and specifications.Real Staffing is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QR coach QP (niet leidinggevend)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob607C814D6F2CCB87482579F5001FBCAB</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QR-coach-QP-niet-leidinggevend_1658680.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een internationale farmaceutische organisatie is voor haar Quality Operations organisatie op zoek naar een QR Coach QP. De site in Noord-Holland heeft het productieproces opgedeeld in verschillende integrated process teams die gaan over het verpakken. Er zijn vier van deze teams, and#233;and#233;n voor blisterverpakkingen, and#233;and#233;n voor niet-standaard verpakkingen, and#233;and#233;n voor vaccines en and#233;and#233;n voor global logistics.Ben jij een apotheker die in de industrie als QP werkzaam wil zijn en ben jij quality minded?Functie omschrijving:- Eindverantwoordelijke voor het releaseproces binnen de IPT - Waarborgen van de kwaliteit volgens GMP- Adviseren op het gebied van compliance- en kwaliteitsgerelateerde verbeteringen-  Goedkeuren van productiegerelateerde onderzoeken - Klachtenafhandeling Secundaire voorwaarden:- Salaris maximaal and#128;60000 incl. o.b.v. fulltime - Reiskostenvergoeding - 25 vakantiedagen en 10 extra roostervrije dagen- Pensioen waarvan 5/6 betaald wordt door de werkgeverFunctie eisen:- Een afgerond apothekersdiploma of vergelijkbaar (in ieder geval universitair)-  Enkele jaren werkervaring binnen de farmaceutische industrie / levensmiddelentechnologie / medical devices- Nederlands en Engels, vloeiend in woord en geschrift- Stressbestendigheid is een van je sterke puntenBeschik je over de gevraagde kwalificaties en wil je meer informatie over deze functie dan kan je contact opnemen met Gwen Reniers 020-5221577and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QR officer voor NoordHolland]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7C13445B73B94BFA482579F5001FBCB7</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QR-officer-voor-Noord-Holland_1658681.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een internationale farmaceutische organisatie met een lokatie in Noord-Holland is op zoek naar een Quality Release officer. Het Center of Excellence Quality is verantwoordelijk voor het aansturen van het kwaliteitsbeleid van de plant in Noord-Holland. Hierbinnen is de Quality Release afdeling verantwoordelijk voor de kwaliteitswaarborging en het vrijgeven van producten voor de markt.Functie omschrijving:- Je draagt zorg voor de compliance van de kwaliteitsprocessen. - Als QRO ben je verantwoordelijk voor de GMP correcte afhandeling van deviaties- Het toezicht houden op de diepgang van het onderzoek en het nemen van CAPAs. - Schrijven van onderzoeksrapporten- Controleren en autoriseren van SOPs- Uitvoeren van systeem audits- Zelfstandig uitvoeren van cGMP inspecties- Review en approval van PQand#146;s- Proactief meewerken aan verbetertrajecten en cGMP Secundaire voorwaarden:- Marktconform salaris van maximaal and#128;60000 incl. vakantiegeld en eindejaarsuitkering op basis van fulltime- Aantrekkelijke secundaire als vakantiedagen en atv dagen en een goede pensioensregelingFunctie eisen:- Minimaal BSc in biologie/chemie/vergelijkbaar- Werkervaring in GMP omgeving bij voorkeur in QA functie- Nederlands en Engels: vloeiend in woord en geschrift- Kennis van Lean is een preBen je geand#239;nteresseerd en wil je meer weten over deze vacature? Druk dan op de and#145;applyand#146; button en upload je cv ter attentie van Gwen Reniers.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager  London  Permanent]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob35FEDAC1155671BD482579F5001FBCC4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-London-Permanent_1658683.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Manager - CRO - London - PermanentMy client is a global CRO based in London urgently requiring a Regulatory Affairs Manager for all stages of the drug development cycle.Responsibilities include:- Provide expert regulatory advice and contribute to regulatory project work - Ensure accurate compilation, management and tracking of submissions - Participate in business development activities preparing regulatory sections of proposals and feasibility reports, regulatory costing and budgets and attend bid defense meetings to meet business needs- Liaise with the Regulatory Affairs Director to plan, organize, compile progress and submit regulatory submissions on a timely basis- Coordinate and#38; manage regulatory and#38; ethics committee submissions and maintain approvals throughout EMEA, Asia Pacific and Latin America regions - Contribute towards the preparation of technical documentation such as IMPDs and IBs which may involve chemical, pharmaceutical, toxicological, pharmacological and clinical aspects of specified regulatory submissions- Review and make recommendations on all relevant documentation e.g. labels, patient information sheets, diary cards etcand#133;to ensure compliance with ICH GCP and#38; country specific requirements- Comply with SOPs, ICH GCP and national regulations as applicableThis is a permanent position based in London paying circa 50k per annum.Please contact Alan Lloyd on 02077587311 for more information. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Manager in Hamburg gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA3542E3EF20C69C9482579F5001FBCD1</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Manager-in-Hamburg-gesucht_1658684.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Sind Sie interessiert an einer abwechslungsreichen und verantwortungsvollen Aufgabe in einem interessanten Medizintechnikunternehmen. Wir suchen fand#252;r unseren Kunden ab sofort einen Quality Assurance Manager im Raum Hamburg.Zu Ihren Aufgabengebieten gehand#246;rt das Qualitand#228;tsmanagement-System, sowie das Koordinieren firmeninterner Maand#223;nahmen eines leistungsfand#228;higen Qualitand#228;tsaudits. Berichterstattung erfolgt direkt an den Head of Quality. Analysen und Optimierung von Prozessen fand#252;hren Sie regelmand#228;and#223;ig durch. Mit Change Control, und den CAPA Prozessen kommen Sie ebenfalls regelmand#228;and#223;ig in Berand#252;hrung. Prozessmanagement- sowie Qualitand#228;tsdokumentationen runden Ihren Alltag ab. Sie verfand#252;gen and#252;ber ein Studium der Naturwisand#172;senschaften (z.B. Biochemie, Biologie, Chemie). Vorteilhaft ist, wenn Sie bereits mit Medizinprodukten der Klasse 2 a und 3 in Berand#252;hrung gekommen sind. Sie haben Erfahrung mit Qualitand#228;tsmanagementsystemen nach ISO 13485 bzw. ISO 9001 sowie Kenntnis and#252;ber alle Anforderungen. Idealerand#172;weise haben Sie bereits die Tand#228;tigkeit des internen Auditors ausgeand#252;bt. Complaint Handling sowie Englisch und Deutschkenntnisse in Wort und Schrift runden Ihr Profil ab.Weiterhin bietet das Unternehmen Ihnen eine interessante Weiterentwicklungsmand#246;glichkeit fand#252;r Ihre Zukunft. Sind Sie bereit fand#252;r eine neue Aufgabe in einem attraktiven Unternehmen?  Dann bewerben Sie sich oder kontaktieren Sie mich direkt unter folgenden Kontaktdaten:a.wydra(at) realstaffing.com Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Marketing Communications Manager, Healthcare  Circa £65K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01EF90A5BEFD3581482579F5001FBCDE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Marketing-Communications-Manager-Healthcare-Circa-and-amp-SHARP16365K_1658685.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Senior Health Communications Manager and#150; London and#150; Circa. and#163;50-56Kand#60;/band#62;After recent developments within their communications team, a leading nutritional company is now looking for a Senior Health Affairs Communications manager. Who will play a major part in educating and developing KOLand#146;s within the nutritional field and work closely with internal stakeholdersand#60;band#62;Focus of the role:and#60;/band#62;Develop, plan and execute a HCP directed programme to increase credibility and recommendation of our products. Set objectives, develop strategies, execute plans and  measure outcomes of communication efforts.Foster relevant stakeholder relationships (KOLs, NGOs etc) in order to support the healthcare strategy and communication in the UKHelp educate the HCP community in the nutritional drinking categoryDevelop online activities to communicate our messages to information seeking HCP audience and direct them to our websites.Work with relevant in house departments e.g. Marketing, Regulatory and Global departments to develop best possible activities and strategies Direct and supervise various agencies to execute agreed activities to time and budget. and#60;band#62;Experience:and#60;/band#62;Strong academic background, ideally with some experience in either FMCG, Nutrition, dietary or potentially pharma products.Strong communication skills and the ability to demonstrate cross-functional workExperience of working with KOL such as Nurses, GPand#146;s, Dieticians and creating communication material based on the target audience.Some understanding of Business, ideally working with BudgetsThey offer a competitive base salary, strong career progression and the opportunity to work on leading Brands. and#60;band#62;Application and#60;/band#62;Should you be interested in discussing the role please  in discussing the role further please contact Sarra Gwilym on 0207 758 7311 or forward your CV following the details below.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ARC Oncologie]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob36BEE1410950E1B7482579F5001FBCEA</referencenumber>
<City><![CDATA[Ile]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ARC-Oncologie_1658686.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Dans le cadre dand#146;un accroissement dand#146;activitand#233; sur deux and#233;tudes en oncologie, un laboratoire international de premier plan recherche un(e) Attachand#233;(e) de Recherche Clinique basand#233; en Ile de France pour une mission de 6 mois renouvelable.Votre rand#244;le :Garant de la qualitand#233; des and#233;tudes, vous and#234;tes en charge des visites de prand#233;sand#233;lection, de mise en place, de monitoring et de cland#244;ture des centres.Vos Missions :- Visites de sand#233;lection, mise en place, monitoring et cland#244;ture des centres. - Monitoring : prand#233;paration des visites, vand#233;rifications et corrections des CRFs avec les investigateurs, suivi des contrats financiers et du paiement des honoraires, mise and#224; jour du classeur investigateur, gestion des traitements, du matand#233;riel et des documents. - Rand#233;daction des rapports de visites, vous rapportez rand#233;guliand#232;rement lactivitand#233; de chaque centre and#224; vos responsables et au (x) Chef(s) de Projets.- Aide and#224; la conception des documents dand#233;tudes (protocole, cahier dobservations, formulaire de vigilance...) et aux soumissions rand#232;glementaires.Votre profil :De formation scientifique, compland#233;tand#233;e par une formation ARC, vous justifiez dand#146;une expand#233;rience de 2 ans minimum en tant quand#146;Attachand#233;(e) de Recherche Clinique, une expand#233;rience en monitoring en oncologie est un plus apprand#233;ciable.Une connaissance des BPCs, des procand#233;dures opand#233;ratoires standard et des protocoles est primordialeVous maand#238;trisez parfaitement land#146;anglais and#224; land#146;and#233;crit et and#224; land#146;oral.Votre personnalitand#233; : Mobile, adaptable, multifonctionnel, et organisand#233;Rand#233;munand#233;ration : en fonction du profilEnvoyez-moi dand#232;s maintenant votre CV au format word afin de postuler and#224; cette offre.Je suis Mathieu Oscoso, consultant Real Pharma, cabinet de recrutement basand#233; and#224; La Dand#233;fense et spand#233;cialisand#233; dans land#146;industrie pharmaceutique. Je travaille avec une large sand#233;lection dand#146;entreprise du secteur : laboratoires pharmaceutiques, CRO et entreprises de biotechnologie ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[HIV Virology MSL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob934E06FABF5D05B3482579F5001FBCF6</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/HIV-Virology-MSL_1658687.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilitiesand#149;Translating highly scientific information into laymanand#146;s terms and#149;Communicating effectively with professors, sales/marketing teams, HCPsand#149;Maintaining and developing relationships with KOLsand#149;Representing Medical Affairs at national and international meetings, congresses and symposiumsand#149;Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice.and#149;Reviewing submissions and formulary applications and establishing/ presenting at advisory boards and#149;Working with cross-functional colleagues in sales and marketingIf this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAE69D67F356C4D82482579F5001FBD02</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Regulatory-Affairs-Associate_1658688.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you looking to progress in your career? If so this could be a great start for you!Due to expansion within our clientand#146;s Regulatory Affairs Team, we have an opportunity for Senior Regulatory Affairs Associate. This is an ideal opportunity for an experienced Regulatory Affairs Associate who is keen to further progress their career.Essential criteria:and#149;Experience with Regulatory Affairs requirements and processes in Medical Devices and Biotechnologyand#149;Degree qualified in a Life Science discipline and#149;Experience in Biologicsand#149;Excellent communication skillsand#149;Ability to work as part of a team dealing with global registrations and provide regulatory support to all operational departments within the companyand#149;Manage regulatory aspects of projects/products, including documentation submitted to regulatory agencies.and#149;Ensure that the documentation complies with applicable regulatory requirementsand#149;Encourage good working relationships with relevant regulatory bodiesand#149;Provide regulatory expertise and guidanceand#149;Attend team meetingsIf you are interested in this position apply now!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Cardiovascular MSL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D9191DDAAA2AAFC482579F5001FBD1B</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Cardiovascular-MSL_1658689.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Providing detailed scientific information in response to requests from the sales team or HCPs-Engaging with external stakeholders in the provision of scientific data in non-promotional fashion-Liasing with the Medical Director in order to develop scientific information materials for the sales team-Providing information at advisory boards, brand meetings and customer programmes-Aiding the development of KOLs through the provision of scientific and clinical data-Abiding  by current ABPI regulations, including maintaining professional standards of contact in line with company regulationsIf this role interests you please contact Orna Mc Donald on 02077587311 or email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[MSL Role Oncology Southern UK]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDB6A9E4E23F163E3482579F5001FBD26</referencenumber>
<City><![CDATA[Wales]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/MSL-Role-Oncology-Southern-UK_1658690.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Tasks InvolvedThe person who fills this role will be expected to maintain and develop relationships with KOLs. They will represent Medical Affairs at national and international meetings, congresses and symposiums. Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice and reviewing submissions and formulary applications will all be part of the role. The MSL will also be expected to work with cross-functional colleagues in sales, marketing, market research, training, health economics, clinical operations and external affairs.If this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Healthcare Communications Marketing Manager  up to £65K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob830039A7D10E0C63482579F5001FBD33</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Healthcare-Communications-Marketing-Manager-up-to-and-amp-SHARP16365K_1658691.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Senior Health Communications Manager and#150; London and#150; Circa. and#163;50-56Kand#60;/band#62;After recent developments within their communications team, a leading nutritional company is now looking for a Senior Health Affairs Communications manager. Who will play a major part in educating and developing KOLand#146;s within the nutritional field and work closely with internal stakeholdersand#60;band#62;Focus of the role:and#60;/band#62;Develop, plan and execute a HCP directed programme to increase credibility and recommendation of our products. Set objectives, develop strategies, execute plans and  measure outcomes of communication efforts.Foster relevant stakeholder relationships (KOLs, NGOs etc) in order to support the healthcare strategy and communication in the UKHelp educate the HCP community in the nutritional drinking categoryDevelop online activities to communicate our messages to information seeking HCP audience and direct them to our websites.Work with relevant in house departments e.g. Marketing, Regulatory and Global departments to develop best possible activities and strategies Direct and supervise various agencies to execute agreed activities to time and budget. and#60;band#62;Experience:and#60;/band#62;Strong academic background, ideally with some experience in either FMCG, Nutrition, dietary or potentially pharma products.Strong communication skills and the ability to demonstrate cross-functional workExperience of working with KOL such as Nurses, GPand#146;s, Dieticians and creating communication material based on the target audience.Some understanding of Business, ideally working with BudgetsThey offer a competitive base salary, strong career progression and the opportunity to work on leading Brands. and#60;band#62;Application and#60;/band#62;Should you be interested in discussing the role please  in discussing the role further please contact Sarra Gwilym on 0207 758 7311 or forward your CV following the details below.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QP  6 Month Contract  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC670E67622AEF4AB482579F5001FBD49</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QP-6-Month-Contract-South-East_1658692.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Requirements:Leading batch assessment and release activities to ensure releases are carried out efficiently, in a timely manner, and meeting relevant regulatory standards. Performing duties of the Qualified Person in compliance with all applicable EU GMP regulations and directives. Improving quality, facilitate Quality management and leading the development of a right first time, quality culture. Relevant experience within a Pharmaceutical Quality Assurance / GMP background. Experience within the Pharmaceutical Industry . Knowledge of process improvement techniques an advantage. Detailed knowledge of GMP requirements for product manufacturing, packaging, licensing, release and post-market responsibilities. Good working knowledge of problem solving and evaluation techniques. Good level of skills in the use of computer based systems, this is to include Lotus Notes, Excel, and Word. Good communication skills to ensure information is taken, used and given at all levels for maximum benefit to the business Minimum requirements Education: Life Sciences Degree Eligible as a QP. Please contact Hemish Ilangaratne on 020 7758 7322 if you are interested in this position or if you know anyone who may be suitable.  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualified Person  12 Month Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA7524A50AC0AF3F0482579F5001FBD54</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualified-Person-12-Month-Contract_1658693.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Requirements: Responsibilities:-Leading batch assessment and release activities to ensure releases are carried out efficiently, in a timely manner, and meeting relevant regulatory standards. -Performing duties of the Qualified Person in compliance with all applicable EU GMP regulations and directives. -Improving quality, facilitate Quality management and leading the development of a right first time, quality culture.  Requirements:- Detailed knowledge of GMP requirements for product manufacturing, packaging, licensing, release and post-market responsibilities. - Good working knowledge of problem solving and evaluation techniques. - Good level of skills in the use of computer based systems, this is to include Lotus Notes, Excel, and Word. - Good communication skills to ensure information is taken, used and given at all levels for maximum benefit to the business.If you are interested in this position or know anyone who might be, please contact Rachel Smith on 020 7758 7322. My client is offering very competitive daily rates to the ideal candidate. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Marketing Communications Manager, Pharmaceutical  Surrey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEAA7F5FB540D3439482579F5001FBD61</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Marketing-Communications-Manager-Pharmaceutical-Surrey_1658694.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Marketing Communications Manager - Surrey - Healthcare - up to and#163;60KOrganisation Description Our client is a large Pharmaceutical company based in Surrey. They are looking to recruit a Marketing Communications Manager on a permanent basis. Job Description Your Main Responsibilities will be:+ Support the 5 year strategic development plan for the UK+ To construct and manage the annual operational plans and budgets for the UK+ In line with the Global Comms strategy, develop communications objectives+ in line with the Global PR Strategy, develop PR objectives+ Communicate plan to Global and Brand team+ Collate information and analyse current market messages+ liaise with medical and NHS team Person Specification You must have/be:+ Scientific or Economics Degree + Minimum of 4 years Pharma experience + Experience of strategic and operation planning for GP and/or Hospital products + Basic understanding of medical aspects of therapeutic area + Professional level English Communication skills + Excellent user of Office programs For further information on this role pleae contact Sarra Gwilym on 0207 758 7311 or forward your CV following the details below.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Database Programmer, Switzerland]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3FE0D2AF4F2C6E53482579F5001FBD6E</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Database-Programmer-Switzerland_1658695.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Clinical Database Programmer, SwitzerlandI am currently searching for an international medical device company a Clinical Database Programmer. Your role here, within the Clinical Data Management department, is to provide database support in order to ensure these databases are as productive as possible. You will be troubleshooting, resolving problems and instructing other data managers in the correct use of the clinical data management system.Other key activities in your daily work life will be reporting any suspected problems to vendors and user support groups, whilst implementing or ensuring the implementation of problem solving techniques. You will be writing and testing data entry screens, creating test files and validating them, also electronically uploading data. This is a strong opportunity for you to progress into a role in a bespoke company, where you will be tested, excited and rewarded for your commitment. You should have experience with clinical databases and experience in a similar data management position.I have excellent industry knowledge, especially in the area of Biometrics and HEOR, and excellent links with hiring managers in the healthcare industry in Switzerland. I would be happy to speak with you about this role or other position I am responsible for. Call Kristin Schirmer on + 41 435080972 or email k.schirmer(at)realstaffing.com for a confidential discussion. Keywords: CDM, Clinical Data Management, Medical Devices, Biostatistik, Biostatistics, Statistics, Statistik, Zurich, Zand#252;rich, Switzerland, Schweiz, Suisse, German, Deutsch, English, Englisch, Clinical Database, Oracle, SAS, Programmer, Clinical Database Programmerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[International Market Access Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC627B39B31CD8F6B482579F5001FBD7B</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/International-Market-Access-Manager_1658696.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[With all the healthcare companies focusing on Switzerland companies in this industry are facing high competition. In this competitive world of healthcare sales it is important to have an excellent market access strategy. I am currently searching for one of my clients, a big, international health care company, a Market Access specialist with an international focus. I am searching for individuals with experience in market access in Switzerland and who are fluent in English and German, to be fluent in French would be an advantage. The company is offering you a position in a global, broad based health care company in an international team. The company is located in the German speaking part of Switzerland. Working for this company means that you will be working for a company which is recognised as a good place to work and which received numerous local, national and international distinctions. As the Market Access specialist you will be responsible for acting as a leadership member regarding market access subjects and you will contribute to the area strategy as well as to the tactic plans. Additionally the market access manager will be responsible for identifying and developing innovative payer solutions to establish and strengthen the portfolio of the company.  I am a recruitment consultant working in Switzerland. I am specialised in HEOR, Market Access and Biometrics. If you want to get further information regarding this positions, or on many more like this, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com. I am looking forward to receiving your current CV as a word document.  Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, Zurich, Zand#252;rich, good place to workand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Direktor für Governmental Affairs & Public Relation]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob855F99593113161D482579F5001FBD88</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Direktor-f-and-amp-SHARP252r-Governmental-Affairs-and-amp-SHARP38-Public-Relation_1658697.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Aufgrund der aktuellen Marksituation sehen sich viel Unternehmen der Life Science Branche neuen Herausforderungen gegenand#252;ber, welche die Bereiche Market Access, Pricing and#38; Reimbursement als auch Governmental Affairs and#38; Public Relation immer mehr in den Mittelpunkt der heutigen und zukand#252;nftigen Strategie rand#252;cken lassen. Ich unterstand#252;tze aktuell die Schweizer Niederlassung eines internationale Pharmaunternehmenes bei der Beseztzung der Position als Direktor fand#252;r Governmental Affairs and#38; Public RelationDas Unternehmen zand#228;hlt als eins der Top 10 Pharmaunternehmen hier in der Schweiz und die Schweizer Niederlassung beschand#228;ftigt mehr als 100 Mitarbeiter in verschiedensten Therapiegebieten wie Onkologie, Schmerz, Herz Kreislauf und viel weitere um das Leben von Millionen von Patienten zu verbessern. Das Unternehmen befindet sich in einer der beliebtesten Schweizer Stand#228;dte umgeben von verschiedensten Skigebieten und direkt an einem See gelegen. Neben verschiedensten Freizeitaktivitand#228;ten bietet Ihnen dieser Standort auch eine sehr gute Infrastruktur. Die Position des Direktors fand#252;r Governmental Affairs and#38; Public Relation fokussiert sich vor allem auf die Schweiz und die Hauptabsatzland#228;nder des Unternehmens. Die Aufgaben dieser Position belaufen sich vor allem auf den Aufbau eines sehr guten Netzwerkes auf politischer Ebene, sei es auf nationaler Ebene als aber auch auf kantonaler Ebene.  Eine der Haupttand#228;tigkeiten dieser Position ist das KOL Management und die Prand#228;sentation des Unternehmens auf verschieden externen Plattformen. Wenn ich Ihr Interesse fand#252;r diese Position oder weitere Position im Bereich Biometrik und HEOR geweckt habe, freue ich mich and#252;ber eine Kontaktaufnahme um mit Ihnen verschiedene Mand#246;glichkeiten hier in der Schweiz zu besprechen. Sie kand#246;nnen mich unter +41 435080972 oder k.schirmer(at)realstaffing.com erreichen. Keywords: Schweiz. Suisse, Switzerland, German, Deutsch, English, Englisch, Governemental Affairs, Pbulic Relations, Market Access, Pricing and#38; Reimbursement, Top 10 Pharmaunternehmen, Pharma, Oncology, Onkologie, Pain, Schmerzand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Market Analyst  Pharma  Marktforschung  Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9DB82CD53F070B27482579F5001FBD95</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Market-Analyst-and-amp-SHARP150-Pharma-Marktforschung-Hessen_1658699.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r den Bereich der Marktforschung sucht mein Kunde einen Mitarbeiter Market Research / Marktforschung.Hier erwarten Sie folgende Aufgaben:and#149; Wettbewerbs- und Marktanalyse and#149; Nutzung externer Datenbanken, u.a. IMS, GPIand#149; Regelmand#228;and#223;ige Preisanalysenand#149; Prand#228;sentation von relevanten Ergebnissen aus den Recherchen  #and#149; Teamarbeitand#149; Auswertung von Strategien fand#252;r das zukand#252;nftige BusinessHierfand#252;r sollten Sie folgende Erfahrungen mitbringen:and#149; Berufserfahrung in der Marktforschung im Pharmaumfeldand#149; Kenntnisse der gand#228;ngigen Datenbanken wie IMS; GPIand#149; Englischkenntnisseand#149; Kenntnisse sand#228;mtlicher Marktforschungsinstrumenteand#149; Teamfand#228;higkeitand#149; Individuelles Arbeitenand#149; Zielstrebigkeitand#149; Kommunikationsstand#228;rkeMein Kunde ist international prand#228;sent und im Gesundheitswesen speziell auf dem Pharmamarkt tand#228;tig. Kontinuierliches Wachstum ist u.a. geprand#228;gt durch den medizinischen Fortschritt, erfolgreiche Vermarktung des Produktsortiments und ein gesundes Arbeitsklima mit flachen Hierarchien.Interessiert? Sehr gerne freuen wir uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior HEOR Manager required]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD2FF2741F22C8E59482579F5001FBDA3</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-HEOR-Manager-required_1658700.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The HEOR Department (Health Economics and Outcomes Research) is the fastest growing department within my client. Due to this I am currently searching for additionally help to support this team based in the German speaking part of Switzerland. The team is focusing on delivering tangible business results to their clients, mostly international pharmaceutical and healthcare industries. As a HEOR Manager working for my client you key responsibilities are, but are not limited to:+ Support and Mentoring of the more junior HEOR Analysts+ Developing of project plans and team leading+ Recommendation of improvements and alternative solutions + Support specific business initiatives+ Implementing the HEOR solutions within the clients organisationMy client is offering you a working place within a fast growing and successful team. To work for this company as HEOR Analyst means that you will support the best international pharmaceutical and healthcare companies worldwide to grow their business and to help more patients. The position will be based in one of the biggest cities in Switzerland. The city is international and is offering you a high living standard. Living in this city means that you will be living near the Rhine and just 1 hour away from the mountains.   I am a recruitment consultant working only in Switzerland, and specialise in HEOR, Market Access and Biometrics. If you want to get further information regarding this position, or on many more like it, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com Keywords: HEOR, Health Economics and Outcomes Research, consultancy, consultant, Analyst, growing, successful, mountains, Rhine, Rhein, international, Top 10 pharmaco, supporting, market research, Marktforschung, Switzerland, Suisse, Schweiz, CHF, urgent, Zurich, Basel, Bern, Geneva, Genf, Geneve, Zug, Zand#252;rich, Frankreich, Deutschland, France, Germany, Ski, Senior Manager, Senior Analyst, Senior, Kristin Schirmer, Real Pharmaand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. Software Validation Specialist  Biopharmaceutical]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0BD73472572BA61D482579F5001FBDAF</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Software-Validation-Specialist-Biopharmaceutical_1658702.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#149;Manage the software validation program, including generating, reviewing and approving validation documents and performing risk and US 21 CFR Part 11 and EU Annex 11 assessments.and#149;Manage the software change control system; assess validation requirements of changes/updates to validated software systems.and#149;Represent and interface with Information Technology and other applicable system owner groups to provide validation and 21 CFR Part 11/Annex 11 guidances in an effective manner.and#149;Trouble-shoot and take the initiative on any QA-related issues for software validation compliance.and#149;Perform internal audits of validated systems to ensure compliance with procedures and protocols.and#149;Conduct vendor qualification audits for software vendors.and#149;Perform training on software validation topics including general software validation, 21 CFR Part 11 regulations and Annex 11 guidelines.and#149;Develop, revise and review Standard Operating Procedures.and#149;Provide assistance as necessary in GMP batch record review and/or vendor qualification audits.and#149;Carry out job responsibilities and assignments safely and maintain a clean and safe work area.and#60;band#62;Candidates must have at least 5 years of experience with biotech or pharmaceutical companies working in a GMP environment to be considered.and#60;/band#62;]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7BA909FA8D398A2D482579F5001FBDBA</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Auditor_1658703.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading manufacturer of recombinant and plasma-based proteins; plasma-based therapies to treat immune deficiencies, alpha 1-antitrypsin deficiency, burns and shock, and other chronic and acute blood-related conditions; products for regenerative medicine, such as biosurgery products; and vaccines. This major pharmaceutical company is looking to hire a full-time auditor.Job Duties: Act as individual contributor on the global compliance auditing team to support internal audit to ensure compliance to company policies and global regulations Lead audits worldwide for all manufacturing facilities Perform external inspections 40 - 50% travel required (domestic and international)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2D8956D053832B46482579F5001FBDC8</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Project-Manager_1658704.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#149;Manage clinical program, including multicenter clinical trials and#149;Compile and/or review key studyrelated documents such as study protocols, IRB Submission Forms, CRFs, SourceDocument Worksheets, SAPs, CSRs, Informed Consents, Regulatory Binder Logs,etc. and#149;Develop and oversee study projectplan to ensure timely completion of key deliverables and#149;Garner strong knowledge andexpertise in the required therapeutic area and#149;Manage CROs and#149;Follow ICH-GCP and other applicableregulatory requirements across all tasks, as well as develop new SOPs as needed and#149;Travel as required (~25%)Desired Skills and#38; Experienceand#149;Masters degree or Ph.D. with aminimum of 6 years in phase I-III drug experience with at least some of thattime in sponsor setting, and at least 3 years directly managing multicenterclinical trials. and#149;Experience with ophthalmic drugs aplus. and#149;Strong knowledge of ICH-GCPguidelines and other regulatory requirements for Phase 1/II clinical trialmanagement and#149;Strong understanding of early stagedrug clinical trial process and#149;Ability to effectively multi-taskand strive in a dynamic start-up environment Company Descriptiona kinase platform company focusing on ophthalmology and is developing new treatments for serious eye conditions. The Companys lead candidate, , targets glaucoma, a condition which damages the optic nerve resulting in vision loss and ultimately blindness. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Immediate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6EB5A62457DD6102482579F5001FBDD5</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Immediate_1658705.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffings medical device clientin the South Bay immediately requires a Quality Engineer.The QE will be responsbile for product development  from early design stages to product implementation in manufacturing. This individual will have some experience in developing and executing the Quality plan for each product development stage.The QE will review new and modified product designs and process documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and conformance to product and quality system requirements.This is a 9 month contract to hire position with a pay rate of and45-70 per hour depending on experience.If this is relevant to your skill set, please aplpy asap.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Los Angeles  Clinical Contracts Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob49102FFCDF8465A7482579F5001FBDE3</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[San Diego]]></State>
<url>http://www.engineerjob.us/job/URGENT-Los-Angeles-Clinical-Contracts-Associate_1658706.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has a need for  a Clinical Contracts Associate that will negotiate with research sites, ensure contracts are written associated with CRMD, and apply clinical principles to solutions of problems with the following experience;-minimum of six plus years of analytical experience or equivalent. -Familiarity with grant and contract requirements, policies, and procedures including, but not limited to:               -Clinical and AdvaMed Code of Ethics on Interactions with                  HealthCare Professionals.               -Knowledge of federal, state and industry rules and regulations governing technical aspects of grants and contracts.                -Requires a demonstrated knowledge of the practices/procedures of the function, company polices, and programs.               -Requires demonstrated written and verbal communication, interpersonal, presentation, technical, analytical, statistical, organizational, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees.              -Must be able to demonstrate and use discretion in exercising work assignments and handle sensitive/confidential information in an effective manner.           - Must have the demonstrated ability to understand and comply with applicable government regulations and Company operating procedures, processes, policies, and tasks.            -Must have demonstrated personal computer skills including a working familiarity with relevant word processing, database, and spreadsheet applications (i.e., Microsoft Word, Excel and Access). Desired Requirements: -Paralegal certification preferred.- Previous related experience administering and/or coordinating grant and/ or contract requests in medical device, biologics, or pharmaceutical company.  -Registered nurse, legal, clinical research associate experience desired. -An advanced degree (i.e., masters and/or doctorate level) as well as professional certifications (i.e., Certified Professional Contracts Manager (CPCM), Certified Clinical Research Professional (CCRP), or related certifications) also a plus.This role needs to be filled by Friday. Please send your resume immediately if interested.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Market Access Director  Global Pharma  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob77B0615B1C75A894482579F5001FBDF9</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Market-Access-Director-Global-Pharma-South-East_1658707.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A fantastic opportunity has arisen within a Global Pharmaceutical organisation for a Global Market Access Director to play an integral role within their new early phase market intelligence hub based in the UK. Committed to developing and launching innovative products, the organisation has an impressive pipeline which makes them a true market leader on a global scale. Situated in the South East of England, the successful candidate would be based in a cutting edge working environment alongside some of the very best professionals within the pharmaceutical industry. As the Global Market Access Director the main accountabilities will be to: and#149; Develop cross-functionally integrated Market Access strategy and#149; Interact with payers to build global relationships and help shape policies towards the targeted therapeutic areas and#149; Lead Value and Access Team and be accountable for reflecting payer perspective in overarching product strategy Successful candidates would have strong communication and project management skills with a deep understanding of payer/HTA environment and evolution on a global level. Candidates must possess a strong commercial acumen and ideally 8 + years relevant experience acquired at pharmaceutical companies, HTA, physician associations or health care consultancy companies. On offer is a Salary of up to and#163;130,000 plus benefits depending on experience. For more information please contact Immanuel Ross at Real Staffing on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Associate  Medical Devices £40k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFDE8220D865BED3C482579F5001FBE07</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-Associate-Medical-Devices-and-amp-SHARP16340k_1658708.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Main tasks (primary responsibilities):  Scientific lead on the project including being the main scientific contact for external parties.  Design Control lead on projects. Provide input to the Early Development team developing the assay. Provide input to the Late Development team verifying/validating the assay. Provide input to the Transfer team as and when required. Supporting the Project Manager in the creation of a project plan.  Accountable for the scientific delivery of the project. Position requirements, qualifications and experiences:  Sizeable industrial or academic post-doctoral experience Proven record in relevant sciences and evidence of the ability to translate knowledge into practical achievements Record of success as responsible study leader in product development or laboratory service projects  Organisational knowledge and proven successful usage of internal company processes (e.g. design control and#38; TQM) Demonstration of the ability to manage employees successfully Technology-spanning knowledge of relevant product areas within and outside the company]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Information Officer  Scotland  £40,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0435EDEA636A114A482579F5001FBE13</referencenumber>
<City><![CDATA[Scotland]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Information-Officer-Scotland-and-amp-SHARP16340000_1658709.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global pharma with an innovative product portfolio and promising pipeline. Recording excellent growth over recent years, expansion demands a new medical information officer to cater for EU based marketed products.Successful applicants should have 2+ years in a medical information function and the flexibility or desire to relocate to Scotland. In return, you will obtain an excellent remuneration package at a company with exciting future prospects.If you are currently on the lookout for a career defining opportunity - please send your updated CV to Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principle Electrical Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFF06242DC0F7B12D482579F5001FBE1E</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Principle-Electrical-Engineer_1664382.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for a Principle Electrical Engineer to join a San Jose based medical device manufacturing company. This successful company is looking to bring on a leading member of their full time design team.Role: As a Principle Electrical Engineer you will be responsible for the design and implementation and full cycle development of electro-mechanical infusion pump units through the complete product design cycle. Responsibilities include high speed digital design, power management, analog design and electric motor control, wired and wireless communication. This role also requires the ability to mentor junior level engineers.Requirements:B.S. in Electrical Engineering or Computer ScienceMSEE preferred10+ years of experience in hands-on design with analog and digital circuitsProven concept to launch development experience requiredLeadership capabilitiesStrong communication skills for a cross-functional roleSalary:and115-140k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance CPM 3 months near Frankfurt]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAFCD406460B93268482579F5001FBE2D</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-CPM-3-months-near-Frankfurt_1664383.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a Pharmaceutical Client who is looking for a Freelance Clinical Project Manager with experience in the diabetes and neurology indication areas for a 3 months contract working at their Office based near Frankfurt am MainYour support is needed in closing down multiple Phase II Studies for a Pharmaceutical Sponsor, working with in the existing clinical research department structure. Key Responsibilities: and#149; Managing the activities of multiple ongoing clinical trials and#149; Managing CRAand#180;sand#149; Author Clinical Study Reports  and#149; Trial Master File review of 3 clinical and preparation for archivingand#149; Support on-going development of clinical trials department Experience:and#149; 3 and#150; 5 years Clinical Project Management experience and#149; Experience in Medical Writing of Clinical Documents and#149; Very strong interpersonal skills and#149; Good GCP/ ICH guidelines knowledgeand#149; Fluent German and EnglishSalary/ Duration: and#149; Start: 15.05.2012 and#149; Duration: 3 monthsand#149; Location: Near Frankfurtand#149; Rate: NegotiableIf you are interested in this position, please send me your updated CV to p.singh(at)realstaffing.com or give me a call on 069/ 264 89 8400. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Data Manager  Sr Clinical Data Manager (telecommuting)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0C49F9E0E7ECEDB0482579F5001FBE38</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Data-Manager-Sr-Clinical-Data-Manager-telecommuting_1664384.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[We are currently seeking a Clinical Data Manager to work on-site with our direct client in South San Francisco. This is a contract role that is scheduled to be at least 12 plus months in duration. and#60;iand#62;The option of telecommuting full-time is available for more senior level candidates. and#60;/iand#62;Clinical Data Manager/Senior Clinical Data Manager, Oncology.Under minimal supervision, perform all data management functions to ensure timely and quality database lock for studies Phase I-III. Perform data management activities for eDC studies conducted in-house as well as overseeactivities of off-shore CRO handling outsourced projects (protocol review,CRF development, database set-up activities, data validation process;medical coding, SAE reconciliation, etc...).----Required Experience:Bachelor degree or above in scientific or related field; commensurate experience in Data Management maybe considered.Minimum of 5 years Data Management experience required (5+preferred).Experience working in an environment where SOP guidelines arent already defined for you (helping to get a CDM department up and running).Proficiency on all related regulations, GCP, and Good Clinical DM Practice.Computer proficiency and knowledge of medical terminology.Project management skills required. Strong oral and written communication skills.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical SAS Programmer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob285D0CD30EFD27EA482579F5001FBE44</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-SAS-Programmer_1664385.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A world renowned Pharmaceutical company based in South San Francisco now has a fantastic opportunity for a Clinical SAS programmer to join a Phase III drug development team to lead on a number of projects and submissions the regulatory authorities. This is an intial 12 month contract opportunity (contract to perm)The development team has seen a number of compounds come through successfully and is now looking to augment its existing team due to an increase in workload. The Clinical SAS Programmer will be involved in a number of activities including:- Develop SAS programs to analyze and report the data generated from clinical trials, quality and improvement initiatives and various ad-hoc analytical studies. - Creating SDTM and ADaM datasets to CDISC standards- Write user-defined, general purpose SAS MACROS. - Program and document online submissions to the Regulatory Authorities.Candidates for this position must have the following skills and experience:- 4+ years SAS Programming experience within the Pharmaceutical Industry- Strong knowledge of SDTM and ADaM data sets- Clear experience within CDISC- Ability to lead and assist with demanding projects]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR BRAND MANAGER  PHARMA CO  SOUTH EAST  £5060k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6CC71C30684645C1482579F5001FBE51</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-BRAND-MANAGER-PHARMA-CO-SOUTH-EAST-and-amp-SHARP16350-60k_1664386.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SENIOR BRAND MANAGER - PHARMA CO - SOUTH EAST - and#163;50-60kA driven Pharmaceutical Company based in the South East is seeking to recruit a SENIOR BRAND MANAGER for their UROLOGY team. Working on a new product this is a fantastic opportunity to be involved in bringing the product to market within the UK. Role/Responsibilities: - Developing and implementing marketing plans for the product - Develop, monitor and execute product strategy - Build and maintain strong relationships with KOLs - Develop market research projects to promote and sustain the product - Develop engaging promotional campaigns and materials - Work collaboratively with the sales team Skills/Experience - Developing marketing plans and strategies - Experience of developing KOL relationships - Knowledge of Market Access - Involved in launching a product into market - Good knowledge of the pharmaceutical market My client prides itself not only on its products but also on its culture and values. If you are interested in working for a large pharmaceutical company who offer a respectful, supportive and encouraging environment then please do not hesitate to get in touch. Warm regards, Shanelle REFERRAL SCHEME: REAL PHARMA OFFER A and#163;200 REFERRAL SCHEME FOR ANYONE WE PLACE WHO YOU REFER TO US. PLEASE PASS THIS EMAIL ON TO ANYONE WHO MAY BE INTERESTED.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT Computer Systems Validation Engineer  San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFA66EDB45178C0C7482579F5001FBE5D</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/URGENT-Computer-Systems-Validation-Engineer-San-Diego_1664387.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client requires a Computer Systems Validation Engineer with the following experience;- Pharmaceutical background (small particle)-IT Infrastructure 6-8 yrs exp- Validating IT Infrastructure-building systems from scratch-Risk Management-Quality Management Systems (from scratch)-validating custom made software- EMPOWER-Debugging-IT background-Team work oriented-good problem solving skills-communication across time zonesThis role needs to be filled by next week. Please send your resume immediately if you are interested.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR BRAND MANAGER  Consumer  London  £60k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob81D7B8340E5C8478482579F5001FBE67</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-BRAND-MANAGER-Consumer-London-and-amp-SHARP16360k_1664388.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SENIOR BRAND MANAGER - Consumer - London - and#163;60k A leading nutrition company is looking for a SENIOR BRAND MANAGER to come on board and drive the launch of their new product to the UK market. Responsibilities: Be involved in all aspects for the new product launch and build the category within the market. In addition, you have high commercial visibility and the opportunity to lead the branding and development of the product. Scope of the role: Should you be successful, this is a growing team and you will have the ability to quickly move into a management level role or move to an international level role. Experience: - OTC/FMCG marketing experience - Healthcare marketing experience - Educated to degree level For more information on this role, please contact Shanelle Mehta on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob135B9151EA4006A0482579F5001FBE73</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-South-East_1664389.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[They will work on the practical aspects of the compounds assigned, from CTAs, ASRs, Scientific Advice requests, MAA preparation, variations, renewals, PSURs. They are willing to pay up to and#163;60 / hour. If interested please get back to me asap and email me an updated CV or alternatively call 0207 758 7322 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacien Affaires Réglementaires]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE35327DCE560AD5482579F5001FBE88</referencenumber>
<City><![CDATA[Ile]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacien-Affaires-R-and-amp-SHARP233glementaires_1664390.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Dans le cadre dand#146;un accroissement dand#146;activitand#233; au sein dand#146;un laboratoire de renommand#233; internationale, rejoignez cette structure en tant que and#171;  Pharmacien affaires rand#233;glementaires spand#233;cialisand#233; dans les dispositifs mand#233;dicauxand#187;. Ce poste est un CDD and#224; pourvoir immand#233;diatement en rand#233;gion parisienne.Pourquoi rejoindre ce laboratoire en tant que and#171; pharmacien affaires rand#233;glementaires spand#233;cialisand#233; dans les dispositifs mand#233;dicaux and#187; ?Laboratoire pharmaceutique franand#231;ais qui dand#233;veloppe, produit et commercialise des produits innovants au niveau national et international.- Vous intand#232;grerez une and#233;quipe pluridisciplinaire qui dand#233;veloppe des mand#233;dicaments indiquand#233;s dans le traitement de pathologies diverses (Neurologie, Ophtalmologie, Oncologieand#133;)- En tant que Pharmacien Affaires Rand#233;glementaires vous serez le garant de la prise en charge de land#146;activitand#233; and#171; dispositifs mand#233;dicaux and#187; and#224; land#146;export de produits innovants qui rand#233;pondent aux exigences pharmaceutiques et aux besoins des patients.Rattachand#233; au Responsable affaires rand#233;glementaires, vous aurez pour mission de :-Marquage CE et enregistrement des produits and#224; land#146;export-Soumettre les essais cliniques auprand#232;s des autoritand#233;s de santand#233;-Mettre and#224; jour les dossiers techniques-Prand#233;parer et soumettre des dossiers de remboursement  et prix-Dand#146;assurer le contrand#244;le des documents publicitaires-Rand#233;pondre aux autoritand#233;s de santand#233; compand#233;tentes Votre Profil :-Docteur en pharmacie-Vous possand#233;dez une expand#233;rience en affaires rand#233;glementaires de minimum 2 ans acquise dans land#146;industrie pharmaceutique.-Un bon niveau dand#146;anglais est indispensable and#224; land#146;oral comme and#224; land#146;and#233;crit. -Esprit de synthand#232;se et dand#146;analyse. Rigueur, organisation et esprit dand#146;and#233;quipe.Envoyez-moi vite votre CV sous format Word. La sand#233;lection des profils se fera dans un premier temps sur les cv envoyand#233;s.Je suis Jennifer Cohendy de Real Pharma, cabinet de recrutement spand#233;cialisand#233; dans lindustrie pharmaceutique. Je travaille avec de nombreux laboratoires pharmaceutiques, dispositifs mand#233;dicaux ou biotechs, ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager  Regio Utrecht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7D62E5B4A0084045482579F5001FBE93</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-Regio-Utrecht_1664391.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Momenteel ben ik voor een directe eindklant in de regio Utrecht opzoek naar een Freelance Regulatory affairs manager. Het zal gaan om een project van 6 tot 12 maandenWe zoeken iemand met een academisch werk- en denkniveau met 3 tot 5 jaar werkervaring. Als RA manager ben je verantwoordelijk voor o.a.:Zorgdragen voor het verkrijgen en onderhouden van registraties die voldoen aan de nationale en Europese regelgeving, conform wet- en regelgeving, teneinde zo spoedig mogelijk een registratie te verkrijgen en onderhouden. Daarnaast zal je deels de volgende taken op je nemen:-Rapporteren van productklachten van de geregistreerde producten-Initiand#235;ren (controleren en goedkeuren) van drukproeven van de verpakkingsmaterialen, SPCand#146;s, bijsluiters en VPIs- Informeren van autoriteiten (College ter beoordeling van geneesmiddelen en Inspectie) en interne partners (medical, marketing en HQ) omtrent registratieprocedures en producten-  Plannen van registraties, vragen van College en Inspectie en interne partners en bewaken van de per registratieprocedure vastgestelde deadline.- Schrijven van locale procedures en werkinstructies, SOPs en OPIs, alsmede deze registreren en onderhouden- Adviseren in BLT omtrent registratie- en vergoedingsaspecten met betrekking tot timing, kansen en bedreigingen- Ontwikkelen en behouden van kennis van Nederlandse en Europese wet- en regelgeving en gerelateerde guidelines m.b.t. Registratie, alsmede van ontwikkelingen in de marktDaarnaast fungeer je als back-up voor het beantwoorden van vragen over alle producten (geregistreerd en niet geregistreerd) die niet door de Medical Information Manager kunnen worden afgehandeld.Beschik jij over bovenstaande kennis en lijkt het je een interessant project? Neem dan direct contact met mij op om het project te bespreken.Met vriendelijke groet,Robert-Jan SmidReal Staffing Groupand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Passionate Global Marketing Manager, Canton Zürich]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA67671BAED922B3C482579F5001FBEA0</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Passionate-Global-Marketing-Manager-Canton-Z-and-amp-SHARP252rich_1664392.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients of the medical devices industry is looking to fill their Global Marketing Manager position in the greater Zurich area.Passionate Global Marketing Manager, Canton Zand#252;richRequirementsThe client is looking for a candidate who is coming from the medical devices background having already worked several years in this medtech industry as well as offering exceptional marketing skills. Further, the candidate should have had exposure in marketing on a global scale. Having work experience with medical devices in the field of heart products is seen as a definite must. Additionally, English is as language skills required and any other language is seen as an advantage.The RoleThe role implies being involved in global marketing activities as well as educating the sales force towards technical matters of the products. You will be in charge of monitoring the sales force to achieve the set financial targets and to adjust in case of deviation. Further, you will also monitor (mentor function) other marketers by overlooking marketing strategies as well as plans which should run accordingly to the set objectives. Of course, as being yourself a marketer, you will develop business plans and marketing strategies, analyze the competition and train the sales force.What do you gain?The company offers an interesting salary package for this position.Further, this company offers opportunities to establish your career path.Additionally, training and support is offered as well as a vibrant environment. The company is globally with more than 5,000 staff represented. Its Swiss location in the Canton of Zand#252;rich offers a great place to be, not only for leisure activities such as mountains and lakes; it is also in a centralized pharma/medical devices industry expanding Canton. Further, the company is a European leader in the medical devices business. I am Corinna Kutzner, a recruitment consultant, working only in Switzerland and specialize for marketing recruitment in Medical Devices/Pharmaceutical industry. If you want to get further information regarding this position, or on many more like it, please upload your CV, best in Word-format. Further, please do not hesitate to contact me on +41 435080972.Key words: Switzerland, Zurich, marketing, sales and#38; marketing, Zand#252;rich, ballons, Switzerland, Europe Middle East Africa, medical devices, international, stents, product launch, product roll out, guide wires, global, English, German, medtech, training, brochures, campaigns, sales forecasts, vascular marketing strategies, promotional tools, technical, scientific components, regional]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Engineer Medical Device company NL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE7FCD55F36E693D482579F5001FBEAD</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Engineer-Medical-Device-company-NL_1664393.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance Engineer- Medical Device company- NLFor this QA Engineer freelance position for Medical Device Company in the Netherlands you will be responsible for:Helping with improvement of procedures, work instructions and other related quality assurance documentation. Implanting changes in QA system assist with audits; review notifications for MDD in different countries and speak to European authorized responsible.We are looking for:and#149;Freelance QA Engineer with experience 1-3years in medical device industryand#149;Education MBO+/HBO  technical or medical  engineeringand#149;Knowledge ISO 13485; Human tissue license and#149;Candidate must speak Dutch and have good English language skills (verbal and in writing)Duration of the project is 5 months.Hourly rate: 40-50Euro all in.Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Associate  Nederland  52K  Auto  Monitoring]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob439CC0E51643D21C482579F5001FBEBC</referencenumber>
<City><![CDATA[Utrecht]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Research-Associate-Nederland-and-amp-SHARP12852K-Auto-and-amp-SHARP150-Monitoring_1664394.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Werk jij graag voor een farmaceut maar wil je wel de zekerheid van een internationaal opererende CRO achter je hebben? Dan heb ik de ideale baan voor jou! Mijn business partner is een globaleand#60;band#62; CRO and#60;/band#62;die in Nederland aanwezig is met een klein maar toegewijd team van Clinical professionals.De bedrijfscultuur kenmerkt zich door een open, altijd veranderende en vooruitstrevende sfeer waarin alle ruimte wordt gegeven voor persoonlijke groei.and#60;band#62;Werkzaamhedenand#60;/band#62;:- Organiseert en begeleidt klinisch geneesmiddelen onderzoek op research sites.- Zorgt ervoor dat alle onderzoeksmedewerkers volledig op de hoogte zijn van de wijze waarop de studie uitgevoerd moet worden en controleert de onderzoeksgegevens. - Selecteert sites, and#60;band#62;onderhoudt contacten and#60;/band#62;met deelnemende artsen en andere investigators. - Coand#246;rdineert de voorbereidingen van de studie en bezoekt de sites regelmatig om ervoor te zorgen dat de gegevens die uit de studie voortkomen betrouwbaar en uniform zijn en voldoen aan de (inter)nationale wet- regelgeving (ICH-GCP, EU-Directive). and#60;band#62;Functie Eisenand#60;/band#62;:- Relevante (bio)medische- opleiding WO- niveau - Minimaal and#60;band#62;3 jaarand#60;/band#62; werkervaring als CRA/Monitor.- Goede schriftelijke en communicatieve vaardigheden inand#60;band#62; Nederlands and#60;/band#62;en Engelsand#60;band#62;Soft-Skillsand#60;/band#62;- Stressbestendig, communicatief vaardig en resultaatgericht - Teamplayer en flexibel- Leergierig en gemakkelijk in de omgang- Goede organisatorische vaardigheden and#60;band#62;Arbeidsvoorwaardenand#60;/band#62;- Salaris tussen and#60;band#62;and#128; 2500and#60;/band#62; enand#60;band#62; and#128;4000 and#60;/band#62;afhankelijk  van je kennis en ervaring-and#60;band#62;Bonusand#60;/band#62; (kan oplopen tot 10%)-and#60;band#62;Lease Autoand#60;/band#62; (met internationale tankpas)-8,33% vakantiegeld-and#60;band#62;Opleidingsmogelijkhedenand#60;/band#62;-and#60;band#62;Thuiswerk mogelijkand#60;/band#62;- Veel meerAls uw ervaring in lijn is met deze vacature en u openstaat om meer te horen over deze zeer interessante uitdaging dan zou ik u willen vragen om zo spoedig mogelijk contact op te nemen met and#60;band#62;Jonathan Gonzalez  and#60;/band#62;Clinical Operations Consultant and#60;band#62;Real Pharma Amsterdam and#60;/band#62;and#60;band#62;020 - 522 1577 and#60;/band#62;of mail uw cv direct via j.gonzalez @ realstaffing.com Ook als u graag wilt horen over de andere vacatures waar ik voor bemiddel of als u iemand weet die openstaat om te horen van een nieuwe uitdaging nodig ik u uit om contact met mij op te nemenand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Altijd CRA willen worden?Monitoring visits CROBrussels >1 ervaring]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob640236B71D9DDA13482579F5001FBECB</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Altijd-CRA-willen-worden-Monitoring-visits-CRO-Brussels-and-amp-SHARP621-ervaring_1664395.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Voor een gerenommeerde CRO in Belgie ben ik op zoek naar een Clinical Research Associate.Deze organisatie gevestigd in de regio and#60;band#62;Brusselsand#60;/band#62;  werkt voor bekende farmaceutische organisatie door heel Belgie.Vanwege de toenemende aanvragen zijn ze het bestaande CRA team  aan het uitbreiden.Het huidige team bestaat uit and#60;band#62;CRAsand#60;/band#62;,CTAs en Project Managers. Als CRA zal jij aan de regionale manager rapporteren.Alsand#60;band#62; CRAand#60;/band#62; zal je verantwoordelijk zijn voor het monitoren van visits en non-visits volgens de bekende protocollen. and#60;band#62;Functie Eisenand#60;/band#62;- Minimaal and#60;band#62;1 jaar and#60;/band#62;werkervaring-HBO/WO Science (richting)- Minimaal and#60;band#62;1 jaar and#60;/band#62;ervaring als CRA (Monitoring Visits)and#60;band#62;Beloningand#60;/band#62;- Marktconform salaris (afhankelijk van je kennis en ervaring)- and#60;band#62;Auto van de zaakand#60;/band#62; (of mobiliteitsvergoeding)- Holiday 8%- 25 vakantiedagen- and#60;band#62;36 uurand#60;/band#62; mogelijk-contract voor onbepaaldetijdand#60;band#62;Meer weten?and#60;/band#62;and#60;band#62;Jonathan Gonzalezand#60;/band#62; Clinical Operations specialist  +31 20-5221577  of j.gonzale @ realstaffing.comand#60;band#62;Keywordsand#60;/band#62;:CRA, CRO, Clinical resarch associate, Brussels, Home based, CRA, CRA I II III IV, CRA, Clinical research associate,Bruxellesand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Manager  NoordBrabant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2614E972F474B6E5482579F5001FBED6</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-Manager-Noord-Brabant_1664396.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Voor and#233;and#233;n van mijn businesspartners in de regio Noord-Brabant ben ik met spoed op zoek naar een Senior Regulatory Affairs Manager. Deze organisatie is een van de snelst groeiende spelers in de farmaceutische industrie. Er heerst een gemotiveerde en gedreven sfeer. De sfeer die er heerst wordt ook uitgedragen door de werknemers.Als Senior Regulatory Affairs Manager binnen deze organisatie zal jij je bezighouden met de ontwikkeling van nieuwe producten. Daarnaast ben je het eerste contactpunt met de regelgevende instanties en adviseer je het management met betrekking tot deze regelgeving. Ook ben jij het aanspreekpunt tussen deze organisatie en haar marketing partners.  Voldoe jij aan de volgende eisen:-Minimaal 4 jaar ervaring met Regulatory Affairs in de farmaceutische industrie-MRP/DCP-MAA-Universitaire graad in Life Sciences (Farmacie, Biologie)-Vloeiend in Engels in woord en geschrift-Management skillsSalaris en Voorwaarden:-and#128; 60.000 and#150; and#128; 85.000 bruto per jaar afhankelijk van salaris-Bonus van max 10% op basis van individuele/bedrijfs prestaties-PensioenregelingKlinkt dit als je ideale volgende stap in je carriand#232;re? en voel je je geroepen om te reageren? Stuur dan je meest recente CV Real Staffing Group of bel 020 522 15 77 en vraag naar Robin Priems.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Business Development  Home office  CRO]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F69AD5803E2E6FC482579F5001FBEE4</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Director-of-Business-Development-and-amp-SHARP150-Home-office-CRO_1664397.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One client, a CRO, is looking to expand the business activities and head count in Germany. In order to achieve success in these fields, the company is looking for the right candidates for the two open positions of Director of Business Development.The key responsibilities include:and#149; Maintenance of existing client contactsand#149; Identifying new business opportunitiesand#149; Acquisition of new clients from the Pharma and Biotech Businessand#149; Develop new sales and marketing strategiesand#149; Participate on symposia, meetings and#149; Achieve Sales goals and develop sales plan for the mid term strategyQualifications:and#149; experience in Sales or in Clinical Development in a CRO or pharmaceutical companyand#149; German resident and and#147;nativeand#148; German language skills and#150; mandatory!and#149; experiences in selling Ph II and#150; IV and#149; Ability to think and work independentlyand#149; Knowledge in planning, conducting and managing clinical trialsAre you interested in that role? Please send us your CV. For further information you can contactElyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CMC Writer  Freiberufler  36 Monate  Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob311F2AF0F4AA5372482579F5001FBEF0</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CMC-Writer-Freiberufler-3-6-Monate-Hessen_1664398.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Einer meiner Mandanten ist eines der weltweit fand#252;hrenden Gesundheitsunternehmen. Mehr als 105.000 Mitarbeiter stehen in 110 Land#228;ndern im Dienst der Gesundheit. Sie erforschen, entwickeln und vertreiben therapeutische Land#246;sungen, um das Leben der Menschen zu verbessern.Insgesamt widmen sich die Mitarbeiter meiner Mandanten der Erforschung der Ursachen von Krankheiten und der Suche nach Ansatzpunkten fand#252;r deren medikamentand#246;se Behandlung ebenso wie der Arzneimittelentwicklung, der Wirkstoffproduktion und Arzneimittelfertigung bis hin zur Auslieferung und dem Vertrieb von Fertigarzneimitteln in die ganze Welt.Das Unternehmen sucht ab sofort einen Freiberufler / Freelance:and#60;band#62;CMC Writerand#60;/band#62;Ihr Profil:and#149; Sie haben ca. 5 Jahre Erfahrung in Regulatory Affairs oder Quality Assurance fand#252;r pharmazeutische Produkteand#149; Sie haben eine sehr gute Erfahrung in CMCand#149; Sie haben ein sehr gutes technisches Verstand#228;ndnisand#149; Sie sind es gewohnt strukturiert und exakt zu arbeitenand#149; Sie haben eine naturwissenschaftliche Ausbildungand#149; Sie beherrschen die Englische Spracheand#149; Zum Vorteil: aseptischen und sterilen Produkteand#149; Zum Vorteil: schreiben fand#252;r Zulassung in USA und Kanada  Ihre Aufgabenschwerpunkte:and#149; Schreiben von and#196;nderungsanzeige fand#252;r vermarktete Produkte and#60;band#62;(Module 3)and#60;/band#62;and#149; Bzw. Sie schreiben die Technischen Dossiers (Module 3)and#149; Sie reichen die Technischen Dossiers bei den lokalen Behand#246;rden einRATE: VERHANDELBARLOCATION: HESSENDAUER DES VERTRAGS: 3-6 MONATE STARTDATUM: 15. MAY  FLEXIBEL ARBEITZEITEN UND REMOTEANTEIL Mand#214;GLICHIm den Einsatzort befinden sich die Forschungs- und Entwicklungsabteilungen, die Produktions- und Logistikorganisation und das grand#246;and#223;te Distributionszentrum. Dieses ist einer von vielen Interessanten Jobs, die ich meinen Kandidaten anbieten kann. Als Personalberater spezialisiert auf die Vermittlung von freiberuflichen Fach- und Fand#252;hrungskrand#228;ften im Bereich der pharmazeutischen Qualitand#228;tssicherung arbeite ich mit vielen Unternehmen in Deutschland, zusammen, die mich stand#228;ndig mit neuen interessanten Projekten versorgen. Falls ich Ihr Interesse wecken konnte bezand#252;glich des Jobs oder vielleicht im allgemeinen, zand#246;gern Sie bitte nicht, mich zu kontaktieren oder mir direkt Ihren aktuellen Lebenslauf zukommen zu lassen. Sie erreichen mich unter +49 (0) 69 264 89 8400 oder p.arroyave(at)realstaffing.com und ich wende mich an Ihnen so schnell wie mand#246;glich.Ich freue mich bald von Ihnen zu hand#246;ren. Selbstverstand#228;ndlich wird unser Kontakt vertraulich behandelt.Besten Dank im Voraus und Viele Grand#252;sse,Pedro Arroyave Recruiting ConsultantMedical Devices EngineeringReal Staffing Group GmbHTel: +(49) 69 264 898 400and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Advisor Pharmacovigilance  Freelancer  RheinMain]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBFDDD8A7BCB1584D482579F5001FBF03</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Advisor-Pharmacovigilance-Freelancer-Rhein-Main_1664399.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein globales pharmazeutisches Unternehmen in der Rhein-Main Region sucht zum nand#228;chstmand#246;glichen Zeitpunkt einen Medical Advisor fand#252;r die Pharmakovigilanz. Es handelt sich um eine Freelance Position von mindestens 6 Monaten mit potenzieller and#220;bernahme.Sie werden in der Pharmakovigilanz Abteilung tand#228;tig sein und sind vor allem fand#252;r die Bearbeitung und Bewertung von eingehenden Nebenwirkungsmeldungen zustand#228;ndig.Fand#252;r diese Position sollten Sie folgende Qualifikationen mitbringen:- Studium der Humanwissenschaften - Mindestens 3 Jahre Erfahrung in der Pharmakovigilanz- Einschland#228;gige Erfahrung in der Bewertung und Bearbeitung von Nebenwirkungsmeldungen- Flieand#223;end Englisch, Deutsch von VorteilBei der Position handelt es sich um eine Vollzeitstelle mit einer Dauer von mindestens 6 Monaten. Nach einer Einarbeitung vor Ort besteht eine home-office Option. Eine and#220;bernahme in Festanstellung ist mand#246;glich.ORT: RHEIN-MAINBEGINN: SOFORTDAUER: OFFEN Wenn ich Ihr Interesse geweckt habe und Sie die Voraussetzungen mitbringen, kand#246;nnen Sie gerne eine E-mail an j.klonek(at)realstaffing.com schreiben oder direkt unter folgender Nummer anrufen: Johanna Klonek Real Pharma + 49 (0) 69 264 89 8400and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance  Clinical Data Manager  12 months  Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEDDA209657EE5A38482579F5001FBF0E</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Clinical-Data-Manager-12-months-Hessen_1664400.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r einen namhaften Kunden im raum Frankfurt suche ich einen freiberuflichen Clinical Data Manager fand#252;r einen langfristigen Einsatz:Aufgaben:- die Auswertung der Daten aus den Clinical Reports - die Programmierung der Plausibilitand#228;ts- und Konsistenzchecks sowie anschlieand#223;ende Generierung und Bearbeitung von Queries- das Aufsetzen und Erstellen von Case Report Forms (CRFs und eCRFs)- das Projektmanagement von Anwendungsbeobachtungen.Ihr Profil:- Abgeschlossenes Studium der Medizinischen Dokumentation oder vergleichbare Ausbildung- Berufserfahrung im DM (mindestens 2 Jahre)- Kenntisse im Daten-Management, Datenbanken und Erfahrung mit unterschiedlichen DM-Tools- eCRF-Kenntisse- Gute EnglischkenntisseStart: Juni/Juli 2012Dauer: 12 Monate+Standort: bei FrankfurtGerne gebe ich Ihnen weitere Informationen zu dieser Stelle.Kontaktieren Sie mich unter: +49 (0) 69 264 89 8400 oder senden Sie Ihren CV direkt an v.klauser(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Exciting Regulatory Affairs opportunity!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob784A93F51C026AE9482579F5001FBF1D</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Exciting-Regulatory-Affairs-opportunity_1664401.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you looking to progress your career? If so this could be a great start for you!My client, a global company in medical technology, is looking for a Regulatory Affairs Associate. This role is great for someone with 1 to 2 years of Regulatory Affairs experience and is looking to progress in their career. In order to be successful at this role you will need to have the following experience:-experience using ERP system-excellent organization skills particularly with Regulatory documentation -have worked with Regulatory Specialists on FCAs-experience in completing TGA annual reports-tracking expiry of all AQIS and MAF import permits-customer service experienceIf you think you have what it takes apply now!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer (mw) Raum NRW gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE59D85865CE341FD482579F5001FBF2D</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-m-w-Raum-NRW-gesucht_1664402.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r meinen Kunden, ein sehr erfahrenes und bekanntes Unternehmen in der Pharma- und Medizintechnik- Branche, suche ich ab sofort einen Quality Engineer (m/w) fand#252;r Medizinprodukte Raum NRW. Ihre Aufgaben:- Bearbeitung von qualitand#228;tssicherungsrelevanten Aufgaben und Fragestellungen im Bereich der Respimatand#174; Produktion - Erstellung, Bewertung, und Freigabe von Abweichungsberichten- Investigation Reports fand#252;r die Produktion bei BImP inklusive Verfolgung und and#220;berprand#252;fung von Korrekturmaand#223;nahmen - Festlegung und Umsetzung von Prand#228;ventivmaand#223;nahmen (and#132;CAPAand#147;)- Erstellung, Prand#252;fung  und Freigabe von GMP-konformen Master- und Vorgabedokumenten fand#252;r die Produktion Respimat (Fertigungspland#228;ne, Arbeits- und Prand#252;fanweisungen, Organisations- und Verfahrensanweisungen, Formbland#228;tter)- Erstellung und Bearbeitung von and#196;nderungsantrand#228;gen- Prand#252;fung und Genehmigung von Versuchspland#228;nen, technischen Berichten, etc.- Durchfand#252;hrung von produktionsinternen Inspektionen, Vorbereitung von  externen Inspektionen- Durchfand#252;hrung von Mitarbeiterschulungen - Freigabe von Bauteilen und Bauteilgruppen in den Systemen SAP und CAQ- Selbstand#228;ndige Bearbeitung von Datenand#228;nderungsantrand#228;genIhr Profil: -  Mehrjand#228;hrige Berufserfahrung im Bereich Qualitand#228;tskontrolle, -sicherung oder in der Herstellung von Arzneimitteln oder Medizinprodukten- Fundierte Kenntnisse der Fertigungstechnologien Spritzguss, Mikrotechnik, Reinigungsprozesse, Montagetechnik, Prand#252;ftechnik- Umfassende GMP-Kenntnisse und Inspektionserfahrung- Sichere Anwendung von Qualitand#228;tstechniken (FMEA, Statistische Methoden: Stichprobenpland#228;ne, SPC, Rand#38;R, DOE, usw.)- Kenntnisse in den gand#228;ngigen MS-Office-Anwendungen - Erfahrung mit Produktionsplanungs- und Qualitand#228;tssicherungssystemen wie SAP und CAQ- Teamfand#228;higkeit, Kommunikationsgeschick- Selbststand#228;ndige, strukturierte und sorgfand#228;ltige Arbeitsweise- Fand#228;higkeit zu analytischem Denken und zielorientierter Land#246;sungsfindung- Sicherer Umgang mit der englischen SpracheHat Sie diese spannende Stelle angesprochen? Ich freue mich auf Ihre aussagekrand#228;ftigen Bewerbungsunterlagen oder Ihren Rand#252;ckruf unter folgenden Kontaktdaten: a.wydra(at)realstaffing(dot)com / Agnes Wydra = +49 (0) 69 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Statistical Programmer  Midlands  £45,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob33284881A5B2A7EE482579F5001FBF3A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Statistical-Programmer-Midlands-and-amp-SHARP16345000_1664403.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An exciting opportunity has arisen within a established medium sized contract research organisation who are in the process of strengthening there technical statistical department. Based in the Midlands the organisation are seeking to appoint a talented statistical programmer that will be responsible for the programming required for the statistical analysis and reporting of clinical trials.The successful candidate will report in to the director of Biostatistics and would be required to perform programming, validation and production of regular statistical summaries of ongoing trials. The ideal candidate must be computer literate, educated to degree level in mathematics, statistics or another subject with a strong statistical component and posses At least one year of experience of SAS programming, with a background in and/or understanding of the specific requirements of clinical research.On offer is a salary of up to and#163;45,000 dependant on experience and the chance to develop your career within a stimulating environment while working for a specialised forward thinking organisation. For more information please contact Immanuel Ross at Real Staffing on 0207 758 7311]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produkt Manager Rx für die Pharmaindustrie in NRW gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8D8A8ACE290EFA27482579F5001FBF46</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Produkt-Manager-Rx-f-and-amp-SHARP252r-die-Pharmaindustrie-in-NRW-gesucht_1664404.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein groand#223;es Pharmazieunternehmen, im Umkreis von Dand#252;sseldorf, sucht zum nand#228;chstmand#246;glichen Zeitpunkt einen Produkt Manager fand#252;r die RX Prand#228;perate in dem Indikationsgebiet Dermtologie. Ihr Aufgabenbereich wand#228;re Schwerpunktmand#228;and#223;ig: and#149;die Erstellung von Marketingunterlagen und die Durchfand#252;hrung von Marketingaktionenand#149;die Durchfand#252;hrung von Markt- und Wettbewerbsanalysen sowie die darauf aufbauende Entwicklung einer Marketingstrategieand#149;die Einleitung zielgruppengerechter PR- und Werbekampagnenand#149;die Koordination der Zusammenarbeit mit Agenturen zur Umsetzung der Marketingaktivitand#228;tenand#149;die Zusammenarbeit mit Meinungsbildnern und niedergelassenen and#196;rzten, z.B. in Advisory Boards oder bei Fortbildungsveranstaltungenand#149;das Initiieren von Marktforschungsstudien und die gewinnbringende Nutzung der relevanten Ergebnisseand#149;das Erstellen kurz- bis langfristiger Budgetpland#228;ne sowie das Marketingcontrollingand#149;die Zusammenarbeit mit dem internationalen Marketingteam Und das bringen Sie mit:and#149;ein erfolgreich abgeschlossenes Hochschulstudium (z.B. Medizin, Pharmazie, BWL mit Schwerpunkt Marketing)and#149;mehrjand#228;hrige (mind. 3 Jahre) Berufserfahrung in der pharmazeutischen Industrie im Bereich verschreibungspflichtiger Prand#228;parate (mit Originalprand#228;peraten)and#149;einschland#228;gige Erfahrung im Bereich Dermatologie Bei Interesse wenden Sie sich bitte an:Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produkt Manager im Bereich Dermatologie gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob41D631975D544425482579F5001FBF51</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Produkt-Manager-im-Bereich-Dermatologie-gesucht_1664405.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein forschendes Pharmaunternehmen ssucht zum nand#228;chstmand#246;glichen Zeitpunkt einen Produkt Manager fand#252;r das Indikationsgebiet Dermatologie. Ihr neuer AufgabenbereichAls Produkt Manager in der Business Unit Dermatologie and#150; Psoriasis - and#252;bernehmen Sie eigenstand#228;ndig und verantwortlich die folgenden Hauptaufgaben und berichten dabei an den Senior Produkt Manager: Eigenverantwortliche Erstellung von Marketingpland#228;nen, Produkt- und Verkaufsstrategien Planung und Umsetzung der Kommunikationskonzepte fand#252;r Produktkampagnen in Kooperation mit PR- und Kreativagenturen Initiierung, Planung und Koordination von Marktforschungsprojekten Initiierung, Planung und Koordination von Fortbildungsveranstaltungen und Kongressen Erstellung der Absatz- und Umsatzplanung fand#252;r das dermatologische Produktportfolio Schulung des Auand#223;endienstes auf die Produktstrategie und Produktbesprechung Planung und Kontrolle des Marketingbudgets Pflege und Aufbau von Kontakten zu Meinungsbildnern und Fachgesellschaften Enge Zusammenarbeit mit Marketingkollegen auf internationaler EbeneWas wir von Ihnen erwartenDie folgenden Anforderungen haben wir an Sie:Abgeschlossenes wirtschafts- oder naturwissenschaftliches/medizinisches Studium Mehrjand#228;hrige Erfahrung im Produktmanagement wahlweise in der Pharmazeutischen oder Konsumgand#252;terindustrie mit dermatologischem Schwerpunkt Erfahrung im Umgang mit Meinungsbildnern Sehr gute MS Office-Kenntnisse Gute Englischkenntnisse in Wort und Schrift Hohes Maand#223; an Engagement, Leistungsbereitschaft und Eigenmotivation Organisationstalent, Teamfand#228;higkeit, analytisches Denken und Handeln and#220;berzeugendes Auftreten, Kontaktstand#228;rke und Durchsetzungsvermand#246;gen Hohes Maand#223; an zeitlicher Flexibilitand#228;t und Belastbarkeit Zuverland#228;ssigkeit und Loyalitand#228;tBei Interesse wenden Sie sich bitte an:Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Product Manger Marketing Manager im Bereich OTC in der Pharmai]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD73E0746600391AB482579F5001FBF5C</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Product-Manger-Marketing-Manager-im-Bereich-OTC-in-der-Pharmai_1664406.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein forschendes Pharmaunternehmen nahe Aachen, sucht zum nand#228;chstmand#246;glichen Termin einen Senior Product Manager OTC. Dieser soll vor allem im Bereich Herz Kreislauf ein Produkt zur Marke aufbauen und wird innerhalb von 6 Monaten zum Group Product Manager befand#246;rdert, ein weiterer Aufstieg mit der Marke ist mand#246;gllich. Ihr Aufgabengebiet: 1.Entwickeln und Ausrichten der OTC-Strategie2.Analyse und des Marktes und Erstellen von Marketing-Konzepten fand#252;r die OTC-Linie 3.Umsetzen der unter (1) und (2) genannten Punkte in Zusammenarbeit mit den Bereichen Med.-Wiss., Vertrieb und Marktforschung und dem OTC-Marketing-Team4.Erstellen und Entwickeln von mittel- und langfristig angesetzten Pland#228;nen (3 and#150; 5 Jahre) fand#252;r die jeweiligen OTC-Produktlebenszyklen5.Erarbeiten von Markterweiterungsansand#228;tzen, z.B.: Line-extender6.Konzeptionieren und Initiieren von Serviceleistungen fand#252;r die Apotheke7.Erstellen eines Aktions- und Maand#223;nahmenplanes mit and#132;B to Cand#147;- Ausrichtung8.Entwickeln einer spezifischen Kundenansprache fand#252;r Apotheker und Endverbraucher9.Planen, Steuern und Kontrollieren des Budgets und ggf. umshiften, sowie der Umsatz- und Absatzdaten der OTC-Produkte10.Aufsetzen geeigneter Maand#223;nahmen zur Sicherung durchgand#228;ngiger Lieferfand#228;higkeit11.Schulen des Auand#223;endienstes zu Fachthemen und Verkaufsinhalten12.Fand#252;hren und fand#246;rdern eines Teams bestehend aus 2 Produktmanagern und einer Marketingassistentin 13.Initiieren und aufsetzen von Marktforschungsstudien fand#252;r die OTC Produktpalette.14.Fachliche Betreuung von einem grand#246;and#223;eren Umsatztrand#228;ger oder mehreren kleinen Produkten15.Enge Zusammenarbeit mit Vertrieb: ADL und RL16.Bewertung von potentiellen neuen Produkten fand#252;r Trommsdorff im Rahmen von Business Development ProjektenAnforderungen Betriebswissenschaftliches oder naturwissenschaftliches   Studium  - Berufserfahrung im OTC-Pharma-Marketing (5 - 10 Jahre)Erfahrung im wissenschaftlichen bzw. Apotheken-Auand#223;endienst Erfahrung in der Teamfand#252;hrung und Team Motivationsichere Kenntnisse im Umgang mit MS-Office-ProgrammenKenntnisse mit Social-Media im InternetProjekt-Management Erfahrungstark ausgeprand#228;gte Kundenorientierunghohes Maand#223; an analytischem und strategischem Denkenstrukturierte Arbeitsweise und Land#246;sungsorientiertheitsolide Anwenderkenntnisse aller Marketinginstrumenteguter Netzwerker and#150; Hohe soziale Intelligenzverhandlungssichere Englischkenntnisseintegrativ, nicht polarisierendTeam Player and#252;ber Hierarchieebenen hinwegsehr gute Gesprand#228;chstechnikenKann begeistern und land#228;sst sich begeisternsehr gutes Zahlenverstand#228;ndniseigenstand#228;ndig durchgefand#252;hrte Laien-/Patientenkampagnen mehrjand#228;hrige PR Erfahrung Belastbare Kenntnisse im Bereich Business Cases und Line Extender Evaluierung Solide Kenntnisse in der Budgetplanung, -steuerung und and#150;verwaltungUmfangreiche Projektmanagementerfahrung Gute Englischkenntnisse Erfahrung in multinationaler Zusammenarbeit Viele Jahre Erfahrung in der Betreuung und Zusammenarbeit mit Entscheidungstrand#228;gernTrifft diese Beschreibung auf Ihre Fand#228;higkeiten und auf Interessengebiet? Dann senden Sie mir Ihren CV an die unten angegebene E-Mail Adresse oder kontaktieren Sie mich telefonisch. Bei Interesse wenden Sie sich bitte an:Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Systems Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA4EA26EB0FB7D0B4482579F5001FBF6B</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Quality-Systems-Specialist_1664407.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A  global medical technology company is seeking an experienced Quality Systems Specialist to joing their Corporate Affairs team. Part of your responsibilities will include: - Ensure only approved Quality Critical Suppliers are used for supply of Quality Critical items.- Ensuring all Government regulations and Quality program requirements and objectives are adhered to.  - Responsible for assisting the development, implementation and maintenance of quality assurance systems and activities.- Ensure the Companyand#146;s implemented quality system is complied with according to the ISO13485 and corporate requirements. - Assist with the implementation and maintenance of the certified ISO 13485 Quality system. - Assist managers with quality documentation, process mapping and reviewing processes.- Assist the BUand#146;s to approve Quality Critical Suppliers to be used only after adequate assessment and evaluation.- Assist in ensuring all quality requirements and objectives are achieved.- Abide byOHand#38;S legislation.Applicants must have:-Tertiary qualification in relevant field- Demonstrated experience Medical Regulatory Quality systems (ISO13485) implementation for pharmaceutical or medical device company- Experience writing technical reports or quality procedures and work instructions. -Soundknowledge of the MS Office suite of software-Sound working knowledge of OHand#38;S / Risk Management / Workers Compensation legislation and principles]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director QA]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1ECF0AA73F732E28482579F5001FBF81</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-QA_1664409.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This position is a senior team contributor, supporting the internal audit program to ensure compliance to company policies and applicable regulations and standards globally.-Provides leadership and guidance in areas of expertise to audit teams to ensure appropriate focus and depth of compliance audits.-Interacts with all levels of internal Management across functions and business units.-Evaluates audit responses for adequacy, including root cause, timeliness as well as utilizes knowledge to facilitate appropriate corrective action.-Serves a cGMP consultant/subject matter expert and provides researched and supported opinions to complex compliance issues]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01E46762925951A7482579F5001FBF8D</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Engineer_1664410.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Responsibilities:-Completes on-site supplier audits for a Class 2 Medical Device-Perform Quality Assurance activities related to product design and development including design control, risk management, supplier management, and product compliant analysis.-Requires up to 20% travel, including international locations-Identifies supplier compliance issues; helps to resolve issues in a timely manner Partners with facilities, divisions, and regions to ensure successful implementation and compliance to CQP / regulations Own and resolve supplier related CAPA(s) -May interface with regulators during regulatory inspections-Utilize the Global Supplier Quality Trackwise System (GSQTS) for maintaining Supplier Quality Records]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Clinical Operations  CRO in Ohio]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB41A298E529BFCA482579F5001FBFA3</referencenumber>
<City><![CDATA[Ohio]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-of-Clinical-Operations-CRO-in-Ohio_1664411.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Director of Clinical Operations - CRO in OhioI am currently recruiting for a Director Clinical Operations to join an exciting CRO based in Cincinnati, Ohio. The company are a global organization with a healthy pipeline and are offering an exciting challenge for any suitable candidates. Below is a snap shot of the position: Position: Director of Clinical Operations Location: Cincinnati (Remote working in not an option) Salary: and140,000 to and160,000 + bonus + benefits Type of Company: CRO Requirements: Strong experience working as a Manager of Clinical Trials / Study Manager etc Experience in therapeutic areas (none specifically) Experience working for a CRO Good level of education This will suit someone who is a Senior Manager of Clinical Trials for a CRO and is looking to take a step up into a new position. Although its a director-level position you will be relatively hands on so someone who is not afraid to get their hands dirty would be ideal. Please send over your resume today if youre interested. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Assoc Director Biostatistics  Growing Biopharm, Flat Org Structure]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA8F2E931480DE367482579F5001FBFB3</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Assoc-Director-Biostatistics-Growing-Biopharm-Flat-Org-Structure_1664412.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The associate director will be working with a cross functional program team as the statistical lead, responsible for statistical activities across multiple studies, and reporting to the program medical director. The ideal candidate is a good communicator, high-energy, self-motivated, and forward thinking. Job Responsibilities: Provide leadership and guidance as the statistical expert on a cross functional program team Represent statistical issues with external parties including regulatory agencies and corporate partners Work collaboratively with internal and external (e.g. CRO) team members to coordinate the planning and execution of biostatistics deliverables Work with data management personnel in the preparation of datasets that are of high quality and in usable format Apply statistical expertise to ensure optimal clinical trial designs, analysis methods and data displays Be accountable for all statistical aspects of protocols and regulatory submissions Contribute to the development of statistical approaches and support for biomarker analysis and translational research. Provide requirements to SAS Programmers to facilitate efficient and effective programming Be responsible for quality assurance of data produced, the validity of the reported results and their statistical interpretation Participate in the establishment of processes and standards for the generation and reporting of data  Requirements: PhD or MS in statistics or related discipline with at least 7+ years of experience in the pharmaceutical or biotech industry Demonstrated ability to effectively contribute to the statistical aspects of clinical protocol design, data interpretation, review and reporting of results for multiple studies and projects Practical experience with application of advanced statistical methodologies to clinical trial design/analysis and with regulatory reporting/submissions Ability to communicate statistical concepts in a clear and concise manner Excellent verbal, writing, and presentation skills. Experience managing outsourced biostatistical services Proficiency with statistical software tools such as SAS, S-Plus, R, EAST Familiarity with regulatory requirements and considerations (e.g. GCP, ICH, 21CFRpart11, CDISC) Positive interpersonal work habits and communication skills and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Contracts Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC4976E046473F051482579F5001FBFBE</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Contracts-Associate_1664413.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Working without appreciable direction, provides technical assistance in negotiating, reviewing, and processing clinical study and research contracts and subcontracts in support of CRMDs clinical research activities. This position will negotiate with research sites, ensure contracts are written in accordance to associated CRMD and regulatory protocols, obtains necessary approvals from senior management for research sites set-up. Work requires the application of business principles/methods, evaluation, ingenuity, and creative/analytical techniques typically acquired in a recognized four-year academic course of study. Within a specialized range of expertise, applies clinical principles to the solution of a variety of problems; customarily and regularly exercises judgment in planning, organizing and performing own work; completes special assignments and projects as required. Assures that quality of services meets internal and external customer requirements. Remains current on developments in field(s) of expertise.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Associate (CRA)  12 month contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF66E8229894ECE55482579F5001FBFC8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Research-Associate-CRA-12-month-contract_1664414.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I am currently recruiting for a Medical Device organisation looking for more of a Clinical Monitoring role than a standard Clinical Research Associate position. The role will potentially be home/field based and we expect that the successful candidate will be based on site monitoring for up to 50% of the time. Although the role is titled CRA as mentioned, it is more of a Clinical Monitoring role as the project has already been scoped out and passed the Ethics committee. The role will be to purely monitor and report back at the end of the process, where everything will be handed back over to the Project Lead. Ideally we would like someone who has experience in Monitoring Medical Devices. The majority of the travel will be between the Midlands and the North of England, but with some further UK travel required. Initially there will be training and induction at the client site in Leeds. JOB SPECIFICATIONS a) Knowledge: 1. Minimum Education Requirements: 1st Degree in Life Sciences, Health Sciences or related field to Biomedical Engineering or equivalent combination of education and experience. 2. Minimum Experience Requirements: 1-2 years (senior 3-4 years) experience of clinical trials management in a medical company preferably with medical devices. 3. Minimum Skill Requirements: Knowledge of clinical study design and management. Relevant experience in implementation of clinical research studies. Working knowledge of international regulatory requirements applicable to clinical research. Awareness of research ethics. Above average oral, written and communication skills. 4. Equipment or Machines Used: Personal computer and general office equipment. b) Problem Solving: Independent judgement is employed in problem solving for project management with supervision. c) Decision Making: Decisions are made subject to established company, departmental and government policies and regulations with supervision. d) Degree of Responsibility: Instrumental in meeting departmental objectives. Must be highly responsible and capable of seeing each project to its conclusion. Please contact for further information.If you know someone that would be interested in this role please contact for referral.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Liason Manager Ireland Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB4E0CA61F37FA9C5482579F5001FBFDF</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Liason-Manager-Ireland-Contract_1664415.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities:and#149;Provide a medical or scientific interpretation of current and newly emerging product and therapy area data to external customers to ensure that they have information relevant to their needsand#149;Provide medical or scientific support to the extended brand team and provide specialist therapy area advice to internal teams (including the field force, marketing, etc)and#149;Manage key medical projects (e.g. IIS studies, post-marketing studies, compliance and adherence programmes) to ensure that companies interacts most efficiently and has optimal contact with customers and key customer networks ,bringing significant value to both the customer and companiesand#149;Work with community groups, patient  organisations and key professional bodies effectively to ensure that companies receives accurate and fair coverage of product and clinical trial-related articles in publications and manage provision of funding within IPHA Code of Marketing  processes and#149;Support MAPOR colleagues in preparing health economic assessments for NCPE and payer groups (e.g. HSE)and#149;Build and develop relationships with key opinion leadersand#149;Research, prepare and provide up-to-date product information for responding to external enquiries for an agreed group of products, ensuring that target response times are met.and#149;Contribute to design, factual accuracy, review and approval of promotional material to support the Companyand#146;s products. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Market Intelligence  Medical Devices  North London]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob83A1E2D634C538AF482579F5001FBFEC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Market-Intelligence-Medical-Devices-North-London_1664416.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Market Intelligence Manager, Medical Devices - North London - Up to and#163;50KCore Responsibilitiesand#149; Responsibility for a number of monthly, quarterly and half yearly industry surveys (data input, and analysis and communication of results)and#149; Selection, purchasing and interpretation of third party market reportsand#149; Environmental, macro-economic and competitor analysisand#149; Benchmarking company performance against key competitors and overall market trendsand#149; Provision of market data and forecasts for Strategic and Business Plansand#149; Commissioning and reporting of ad hoc market research projectsAdditional QualitiesStrong Commercial Experience and ability to work in a smaller teamFor further information please contact Sarra Gwilym 0207 758 7311 or forward your CV below.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[EMEA Product Manager  Orthopaedics  North East  £45  60k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob486F2A6D1BF83BE4482579F5001FBFF7</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/EMEA-Product-Manager-and-amp-SHARP150-Orthopaedics-and-amp-SHARP150-North-East-and-amp-SHARP16345-and-amp-SHARP150-60k_1664417.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[EMEA Product Manager and#150; Orthopaedics and#150; North East - and#163;45 and#150; 60kBeing responsible for an orthopaedic portfolio, this is a fantastic opportunity to join a highly successful company and team in developing and executing their market strategies. Role and responsibilities: - Working closely with the sales and commercial teams - Set strategic direction and long term plans for the product - Plan the launch of new products - Develop and maintain relationships with KOLs and customers - Create clear, innovative messaging - Ability to manage the cross-functional implementation of the plan The role is to be office based in the North East with roughly 40% of travel across Europe, Middle East and Africa. There are excellent career opportunities on offer for the successful candidate including progressing up to Group Product Manager, opportunity to work across a range of cultures and geographies and the opportunity to take a side step into another division of the company. Skills and experience: - Educated to degree level - Preferably have an MBA or diploma in Marketing - Experience in strategic planning - Ability to communicate at all levels - Orthopaedic, devices, or relevant healthcare experience - Proven ability to analyse quantative/qualitive data - Proven track record in developing and executing marketing plans This is an outstanding opportunity and one not to be missed. For more information, please contact Shanelle Mehta on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principle R&D Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6C296FB354C34B8F482579F5001FC00A</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Principle-R-and-amp-SHARP38D-Engineer_1664418.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Calling all Rand#38;D Engineers!Real Staffing Group is urgently seeking a Senior Rand#38;D Engineer for a Leading Medical Device company in the Bay Area. This ground breaking medical device company is looking to bring on a full time employee with a strong mechanical engineering and design background with experience in the disposable medical device fieldRole: As a Senior Rand#38;D Engineer, you will be responsible for the full life cycle design and development of disposable device components, as well as related testing and analysis for product and systems. Essential skills and qualities include project planning and management, cross-functional communication between design team and board members, and ability to independently perform assignments as well as give technical guidance to lower level personnel.Requirements:B.S. in Engineering (Mechanical Engineering desirable)6+ years of engineering experience in regulated field4+ years of disposable Medical Device experienceMust have experience with disposable device designLeadership capabilitiesStrong communication skillsSalary:and85-110k depending on experienceIf you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Program Manager Managed Care Marketing]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8824762D8E141153482579F5001FC016</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Program-Manager-Managed-Care-Marketing_1664419.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leader in the diagnostics company is currently looking to bring more value to their close knit and cross functional Managed Care Marketing team. With endless opportunities for career progression and leadership opportunities you will wear many hats and work alongside the market access team. This is a dynamic and rewarding individual contributor role reporting to the Senior Director Managed Care Marketing.The Role: -Marketing position requiring expert communication and presentation skills/ power point -Highly analytical program manager role (emphasis in quantitative data) serving as a liaison cross functionally with clinical, regulatory, market access, and health economics. -Convert analysis of economic models and cost benefit models into payer tools -Responsible for packaging data and marketing strategy for field reimbursement professionals in efforts to support payer relations, coding, and coverage -You will work closely with product marketing and building strategy- more downstream than upstream focus-Present the visibility of gaining coverage with medicare and payers-Private payer market research- payer roundtables/ad boards, synthesis of data and summarizing results for internal and external use-Deliver value propositions pertaining to managed care marketing projects]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Customer Insight ManagerContract Maidenhead]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDDF553F8B002C5A0482579F5001FC02B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Customer-Insight-Manager-Contract-Maidenhead_1664420.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Role - Use diverse information sources to identify changes in consumer, shopper and retailer attitudes and behaviours - Analyse diverse data and information sources to evaluate competitorsand#146;, WCH and retailersand#146; strengths and weaknesses to help drive brand and trade strategy development - Be the brand advocate and#150; proactively work to maximise: rate of sale, range, space, listings and display of WCH brands in key retailers/wholesalers Space planning and the ability to develop and present fact based selling arguments and presentations for our retail and wholesale customers. Experience/Skills and#149;Experience in category management, sales, retail or trade marketing and#149;UK OTC experience (preferable) For Further information, please call Moushmi Patel on 0207 758 7322  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electro Mechanical Systems Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA841AD19862A75AB482579F5001FC037</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Electro-Mechanical-Systems-Engineer_1669911.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for a Senior Electro Mechanical Systems Engineer to join a San Jose based medical device company. This successful manufacturing company is looking to bring on a leading member of their full time team.Role: As a Senior Electro Mechanical Systems engineer you will be responsible for the post-market re-design and testing of sophisticated electro-mechanical systems and components as well as the generation of analytical models and test methods. Self-direction as well that the ability to lead others is important to this roles success. This role requires the capability to analyze and develop advanced algorithms for systems involving motors, actuators and sensors.Requirements:B.S. in Mechanical Engineering10+ years of experience in mechanical engineering fieldProven record in design, development modeling and testing of electro-mechanical systemsFamiliarity with C++ and VB codes, also LABVIEW scriptsLeadership capabilitiesStrong communication skillsSalary:and95-135k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Programmierer Raum Hannover sofort zu besetzen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE878B965B1540EE6482579F5001FC043</referencenumber>
<City><![CDATA[Niedersachsen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Programmierer-Raum-Hannover-sofort-zu-besetzen_1669912.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Die Real Staffing Group ist eine spezialisierte Personalberatungsagentur fand#252;r die Pharma- und Medizintechnikindustrie. Mein Kunde, der in Raum Hannover ansand#228;ssig ist, suche ich zur Erweiterung des Teams, einen erfahrenden Programmierer.Programmierer Aufgaben:Es geht um die Entwicklung sowie Verfeinerung medizinischer Systeme. Sie sind zustand#228;ndig fand#252;r die Benutzerschnittstellen (GUI) sowie grundlegende Datenstrukturen. Sie bekommen Projekte, die Sie selbst steuern. Sie sind ebenfalls fand#252;r Lasten- und Pflichtenheften verantwortlich.Profil:Studium der Informatik, Elektrotechnik o.and#228;.2jand#228;hrige Berufserfahrung in Web- und Desktopanwendungen sollten vorhanden sein. Sie sollten sehr gute Kenntnisse in der Programmierung mit C++ haben. Von Vorteil waren Erfahrungen in: QT, XML, PHP, Java und SQL. Sehr gutes Deutsch wird vorausgesetzt.Sie wollen etwas fand#252;r die Allgemeinheit tun? Sie brauchen ein Herausforderung? Dann bewerben Sie sich jetzt als ProgrammiererSenden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Principal Quality Engineer  Orange County]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB3CDBB9A1AE7404E482579F5001FC04F</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/URGENT-Principal-Quality-Engineer-Orange-County_1669913.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My Client has an urgent requirement for the following;A Principal Quality EngineerJob Family Summary Quality Engineer is responsible for quality evaluation and control of the product development projects. Works cross-functionally in the product design and or maintenance of product design changes. Ensure that appropriate development activities are in place, consistent with business objectives and regulatory requirements.What is expected of you for success in your roleand#149; Applies intermediate understanding of regulatory requirements for Medical Devices (cGMP, FDA, ISO, etc.) to support work with little or no supervision.and#149; Works to understand complex functional situations by paying attention to the details of the tasks at hand and by breaking them down into smaller pieces.and#149; Proactively develops and maintains broad knowledge of the technical disciplines in own functional area(s); applies broad knowledge of trends and best practices in a manner that ensures exceptional performance and results.and#149; Uses deep subject matter/functional expertise, influence and process skills to help internal/external customers and stakeholders identify and meet their high priority needs while considering cultural and diversity implications.and#149;Encourages informed Risk-taking and acts as a catalyst for innovationQualifications:and#149;  Bachelors degree in engineering or quality and 3 years of experience as a design or quality engineerand#149; ASQ (or equivalent) Certified Quality Engineer (CQE) or Software Quality Engineer (CSQE)and#149;  2-4 years direct experience in a Product Development or Rand#38;D Organizationand#149;   Excellent communication skillsStart working next week, please send resumes immediately.KeywordsDesign Assurance, Quality Assurance,]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead Clinical SAS Programmer  Illinois  Contract  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob52F0A145BE8AF0BC482579F5001FC05A</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Lead-Clinical-SAS-Programmer-Illinois-Contract-6-Months_1669914.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a leading Pharmaceutical Company based in Illinois, now has a great opportunity for a Lead Clinical SAS Programmer to work on Phase II and Phase III Oncology studies.  This is a 6 month contract paying and65 - and75 p/h.This leading Pharmaceutical Company has recently seen a number of successful compounds pass the early phases of the Clinical Trial process and due to an increase in workload is seeking a strong Lead Clinical SAS Programmer to lead on the full project life-cycle of phase II and III Trials within Oncology.  This will include supporting the design of the Statistical Protocol and Statistical Analysis Plan, the implementation of the plan and the creation of Tables, Listings and Graphs for Clinical Study Reports and Regulatory Submission Documents.Candidates for this position must have the following skills and experience:- Masters in Computer Science or related field- 5+ years experience within the Pharmaceutical Industry- Proven Track Record in creating TLGs for CSR and Submission Documents- Knowledge of CDISC, SDTM, ADaM- Strong Communication skillsApply now for immediate consideration or contact Tom Bakker on 312-453-9088. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacien Qualité Produits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob009E58AACBFCB6E8482579F5001FC066</referencenumber>
<City><![CDATA[Lyon]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacien-Qualit-and-amp-SHARP233-Produits_1669915.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Rejoignez un laboratoire de dimension internationale,  en tant que Pharmacien Qualitand#233; Produits dans le cadre dand#146;un CDD jusquand#146;and#224; fin Octobre 2012 (Dand#233;marrage ASAP).Vos missions: Rattachand#233;(e) au Directeur Qualitand#233; et au Pharmacien Responsable et au sein dand#146;une and#233;quipe de 5 personnes, vous serez le garant de la qualitand#233; des produits et du maintien de land#146;activitand#233; pharmaceutique du laboratoire selon les BPF, le code de la santand#233; publique et les dossiers dand#146;AMM.Vous serez amenand#233;(e) and#224; :and#149; Gand#233;rer le suivi des rand#233;clamations et des non-conformitand#233;s and#149; Conduire et gand#233;rer les audits sous-traitants/fournisseursand#149; Suivre les and#171;Revues annuelles produits and#187;and#149; Approuver les dossiers techniques produitsVotre profil:- Pharmacien avec thand#232;se (obligatoire) ;- Expand#233;rience de 2 ans ;- Maand#238;trise des rand#233;fand#233;rentiels : BPF et de la production de mand#233;dicaments and#145;formes sand#232;chesand#146; (chimiques) ;  - Anglais professionnel/ courant ;Envoyez-moi vite votre CV sous format Word.Je suis Benjamin MAURICE de Real Pharma, cabinet de recrutement spand#233;cialisand#233; dans lindustrie pharmaceutique. Je travaille avec de nombreux clients CRO, laboratoires pharmaceutiques ou biotechs, ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Marketing Manager  South East  £6070k plus excellent benefits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF1620E6A367CB22E482579F5001FC073</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Marketing-Manager-and-amp-SHARP150-South-East-and-amp-SHARP16360-70k-plus-excellent-benefits_1669916.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Marketing Manager and#150; South East - and#163;60-70k plus excellent benefitsA world class Pharmaceutical company is seeking a Marketing Manager to lead and deliver on an established diabetes portfolio.Responsibilities:-Develop and measure a 3-5 year strategic marketing plan-Manage the strategic development of the market and product portfolio-Develop product promotional budgets and Pand#38;L-Work cross functionally with external and internal stakeholders-Forecast product volumes-Manage the brand development process-Line manage, develop and train the product management teamExperience:-Knowledge of the Pharmaceutical Industry in a customer facing role-You will have two direct line reports so having managerial experience is desirable but not essential. -Marketing process and strategic planning-Market modelling and forecasting-Financial management and budgetary skills With excellent career progression through internal opportunities, training and development you will find this Pharmaceutical company to be supportive and encouraging of its employees.For more information on this role please contact Shanelle Mehta on 0207 758 7311]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Investigator  Contract positions  2 months initially  All expenses]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob724246F3F87D3BAE482579F5001FC080</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Investigator-Contract-positions-2-months-initially-All-expenses_1669917.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Description:and#149; Lead Responsibilities include investigations related to all deviations including process and equipment deviations and deviations in manufacturing. and#149; Responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities:and#149; Have a fundamental understanding of the investigation process as it applies to manufacturing issues and#149; Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical.and#149; Be able to use that knowledge to investigate process deviations and atypical results and identify root cause Requirements and#149; BS or MS in a scientific or engineering discipline with 3+ years. and#149; A strong technical background in a cGMP and Quality environment is required. Prior experience with investigations including conducting and writing investigations preferred. and#149; MOST CRITICAL: Knowledge of the processes used to manufacture biologics and a understanding of Trackwise and practices used to investigate, document and correct atypical events that occur in the process This is not an entry level position - you MUST have at least 3 years working for a pharmco / biotech / biopharma. Nor is this a senior level position. It would ideally suit a Quality Assurance Specialist who experience of investigations. Starting ASAP - this is an URGENT requirment. APPLY NOW and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Quality Assurance Indiana  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2A32A134DB5B5B28482579F5001FC08C</referencenumber>
<City><![CDATA[Indiana]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-of-Quality-Assurance-Indiana-Contract_1669918.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A global Medical Device company is seeking to hire a highly qualified individual to fill the position of Director of Quality Assurance.  The company, located in Indiana, is a leader in the development and manufacturing of non invasive medical devices.  With annual sales approaching the and10 billion mark the company is focused on hiring individuals who are passionate about strengthening patient care and increasing efficiency amongst healthcare professionals.The Director of Quality Assurance will report to the Vice President of Quality Assurance and is responsible for developing, managing and implementing projects, and maintaining a satisfactory level of compliance.  The Director will have 12 direct reports which will receive quarterly performance reviews to further their development.  This position is also responsible for tracking all quality activities and identifying best practices.The candidate must meet the following requirements:- B.S. - 5+ years experience in Medical Device industry- GMP and GCP experience- Extensive knowledge of FDA and Regulatory agency regulations- Exceptional managerial skills- Ability to communicate well with othersIf you are interested in this position please apply now or contact Dana Leone at 312-453-9088 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Officer  £3032k Global Generics]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1F1895F2D47DB91E482579F5001FC099</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Officer-and-amp-SHARP16330-32k-Global-Generics_1669919.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Officer: and#60;band#62;and#163;30-32kand#60;/band#62;-The focus of the role will be submission of new generic Marketing Authorisation Applications for retail products via the Centralised , Decentralised, or Mutual Recognition Procedures. -You will be experienced in the preparation, compilation, review and submission of high quality dossiers in accordance with European requirements and legislation and would preferably have one to two years of regulatory experience (which may encompass some experience in another related pharmaceutical role).  -You will have an understanding of European regulatory procedures, requirements and guidelines.-You will have a degree in a Life Sciences or a Pharmacy related subject or equivalent industrial experience in a European regulatory role. -Previous CMC experience (or a demonstrated technical aptitude) and familiarity with the scientific content of the dossier is also preferred.-You will be an excellent communicator (verbal and written) and be confident in representing the team during strategic and technical discussions, including participating in project teams, as required.  You will enjoy the challenge of working under pressure whilst consistently ensuring that internal and external deadlines are met. If you are interested to find out more contact n.hopkins(a)realstaffing.com or call 02077587311 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Egineer in Hamburg gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4D9BC91847FDA743482579F5001FC0A5</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Egineer-in-Hamburg-gesucht_1669920.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r meinen Kunden, ein innovatives sowie bekanntes Unternehmen im Hamburger Raum, wird fand#252;r den Bereich Medizintechnik ein Quality Engineer gesucht.Zu Ihren Aufgaben gehand#246;rt die Betreuung der Serienfertigung fand#252;r einen zugewiesenen Fertigungsbereich. Sie arbeiten im Rahmen eines interdisziplinand#228;res Sustaining Engineering Teams (S.E.) bestehend aus Rand#38;D, Einkauf, Supply Chain Management und Produktion zusammen.Das and#196;nderungsmanagement fand#252;r bestehende Produkte und Prozessesowie Prand#252;fplanung, Prozessand#252;berwachung und Auswahl der Prand#252;fmethoden liegen ebenfalls in Ihren Hand#228;nden. Bewertung von Non-conforming products bei Q-Abweichungen sowie Lieferantenbetreuung runden Ihr Profil ab.Sie bringen ein abgeschlossenes Ingenieurstudium und ca. 3-5 Jahre Berufserfahrung oder den Techniker mit entsprechender Berufserfahrung mit.Kenntnisse and#252;ber Methodenkompetenzen (Design- und Prozess-FMEA), sowie Prand#252;fmittel- und Maschinenfand#228;higkeitsuntersuchung gehand#246;ren ebenfalls zu Ihren bereits erworbenen Kenntnissen. Wenn Sie erste Erfahrungen mit Lieferantenauditierungen sowie sehr gute Englischkenntnisse mitbringen, freue ich mich auf Ihre Bewerbungsunterlagen unter folgenden Kontaktdaten:a.wydra(at)realstaffing.com/ Agnes Wydra - +49 (0) 69 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Trial Assistant  6 months  Brussels]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5BA66D23CE1174AF482579F5001FC0B2</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Trial-Assistant-and-amp-SHARP150-6-months-and-amp-SHARP150-Brussels_1669921.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is urgently looking for a senior CTA consultant for a period of 6 months with possible extensions. Primary activities include, but are not limited to: - Assemble and provide support for timely Clinical Trial Submissions and availablity of Essential Documents for clinical trials. - Act as relationship manager with 3rd party vendors or with support groups such as ancillary supplies management - Create Essential Documents Repository. - Assemble and track availability of all essential documentation required for study conduct. - Provide professional presentation of study materials for investigator/vendor or country operations meetings - Safety reporting tracking - Liaise with sites and in house departments to ensure appropriate regulatory follow-up - Organization and documentation (minutes) of project team meetings - Site Visits: QC of trial binders and other study documentation for completeness, consistency and accuracy. Operational and project support activities, including, but not limited to: - archiving and/or accountability for completeness of Trial Master File - Update, maintain and monitor CTMS to allow accurate project management, regulatory reporting and clinical grants payments - Follow-up/check final accountability of IMP and return or destruction as appropriate - Review study budgets/clinical trial agreements for consistency with study protocol  - Updating of clinical and study planning databases Qualificatons, Skills, and#38; Experience: and#149; Written and spoken fluency in English and Dutch. and#149; Excellent computer skills: MS Office (mainly Word, Excel, Outlook, and PowerPoint) and intranet and#149; Very high accuracy and#149; Flexibility and hands-on initiative and#149; Sense of responsibility and#149; Basic knowledge of medical terminology is an asset and#149; Capacity to work autonomously and in a team  Education/experience: - bachelor degree (e.g. medical assistant, or paramedical education) or relevant work experience in clinical research fieldWe will endeavour to respond to your application ASAP. However, there may be times when it is not possible to reply to all applications, due to high volumes of enquiries. This is sometimes the case for unsuccessful applications to one of our vacancies. We apologise for this and can reassure you that we will keep your details and contact you in the future should any suitable positions arise.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interesting contract in Boston for Statistical programmers.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5C42F09CB919DB0B482579F5001FC0C8</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Interesting-contract-in-Boston-for-Statistical-programmers_1669922.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, one of the worlds leading companies in the Pharmaceutical Sectors, now has a fantastic and interesting opportunity for a Senior SAS Programmer.  The position is based in The greater Boston area and will be a 12 month initial contract.Working for one of the worlds leading companies the Senior SAS Programmer will join the firm at a very critical time.  My client is currently working towards a number of FDA submissions across phases II and III and requires the Senior SAS Programmer to lead on the project.  The role will include taking the raw trials data and converting into SDTM and ADaM formats.  In addition, the Senior SAS Programmer will be mentor junior programmers.Candidates for this position must have the following skills and experience:- 10+ years experience within SAS Programming- Proven track record within the Pharmaceutical Industry- Previous experience of leading a project / submission - Proven skills and experience within SDTM and ADaM DataApply online now for immediate consideration or contact Jord Teeuwen on 617-737 -8101.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Officer  Medical Device  The Netherlands]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob70D8E1CD9E97482D482579F5001FC0D3</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Officer-and-amp-SHARP150-Medical-Device-and-amp-SHARP150-The-Netherlands_1669923.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance Officer and#150; Medical Device and#150; The NetherlandsAs a freelance QA Officer for medical device company you will be responsible for:1. Assisting with inspections (searching and providing the right documents) 2. Assisting and reviewing workflow procedures 3. Administrative tasks (as an outcome of contact with different suppliers) We are looking for: and#149;QA officer experience 1-3 years in medical device industry and#149;Education MBO+/HBO  technical or medical  engineeringand#149;Knowledge ISO 13485and#149;Excellent English language skills (speaking and writing).Duration of the project is 5 months.Hourly rate: 40-50Euro all in.Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Preclinical Biostatistician in Boston.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5797A370F60E0EFF482579F5001FC0E1</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Contract-Pre-clinical-Biostatistician-in-Boston_1669924.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a leading Pharma Company based in The Great Boston Area, now has a fantastic contract opportunity for a Pre-Clinical Biostatistician.Working for this market leading company you will be working on a variety of compounds within Biologicals across animal and human vaccines.  This role will involve working closely with senior scientists, CRAs and trial coordinators.  You will be expected to work heavily in study, protocol and SAP design.  In addition you will be heavily involved in PK/PD work. Furthermore, candidates will be working closely with the FDA and other bodies to ensure regulatory compliance.Candidates for this position must have the following skills and experience:- PhD within Statistics or related field- 5+ years Pharmaceutical Experience- Pre-Clinical / Non-Clinical or Early Stage Experience- FDA or other regulatory body submission experience- SAS KnowledgeThis is an initial 12 month contract with extensions.Apply now for immediate consideration or contact Jord Teeuwen on 617 737 81 01.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Clinical Data Manager  South Germany  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9C1EEC62CC3D669482579F5001FC0ED</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-Clinical-Data-Manager-South-Germany-6-Months_1669925.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I have a fantastic 6 month contract position for a Lead Clinical Data Manager for a leading Pharmaceutical client based in South Germany for a July start.As a Clinical Data Manager you will be responsible for tracking and managing the biometric activities for outsourced clinical trials on large Phase II and III studies for a number of new set-up studies.You will be required to deliver input, review and approve CRO deliverables as required per SOPs and tasklist, ensuring that all biometric activities are completed ontime and within budget. You will be responsible for performing quality checks and ensure any Data Management issues are resolved providing full communication to the sponsor at all times. The role will also require you to act as a Data Manager assisting the team when necessary.Experience:-5 years + Clinical Data ManagementCRO monitoring / surveillance experiencePhase II-III experienceEDC system experience advantageousFluent English (German nice to have)RATE: Negotiable (Depending Upon Experience)DURATION: 6 Months (Extension possible)LOCATION: Near MunichSTART DATE: June/July 2012If you are interested in this position and want to discuss this in greater detail please do not hesitate to contact Vincent Klauser at Real Pharma for more information on + 49 (0) 69 264 89 8400 or email v.klauser(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract SAS Statistical Programmer  Germany  12 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob28640F1CC14C5D35482579F5001FC0FA</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-SAS-Statistical-Programmer-Germany-12-Months-_1669926.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a leading Pharmaceutical company in Germany with a major market presence both nationally and internationally due to their pioneering approach in the manufacture of leading Pharmaceutical products and their large investment policy into drug development.I have an excellent 12 month freelance / contract opportunity for a SAS Statistical Programmer to work for my client near Frankfurt due to the an explosive pipeline of new drug development that requires additional support from Statistical programmers.You will be providing SAS programming support to a number of clinical trials as part of a submission package to the FDA. Therefore you will be creating and validating analysis datasets, Tables, Figures and Listings.Experience:-5 +  years SAS Statistical Programming within the Pharmaceutical Industry SAS BASE / MACRO / STAT / GRAPH Creating and Validating Analysis Datasets, Tables, Figures and Listings Knowledge of CDISC - SDTM / ADaM is desirableExcellent communication skills in English (German is advantageous) This is a fantastic opportunity to make lasting impression with one of the Top 10 Pharmaceutical companies in the World and have a prestigious client on your CV and could lead to a long-term relationship with this client based on performance.Rate: Up to and#128;650 Per Day (Depending upon experience)Duration: 12 Months (6 Months Extension possible)Location: Near Frankfurt, GermanyStart Date: ASAP If you are available and interested in this position please contact Vincent Klauser at Real Pharma on + 49 (0) 69 264 89 8400 or email v.klauser(at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Manager  Leidinggevende functie  tot 82k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob50B2C128E351688D482579F5001FC106</referencenumber>
<City><![CDATA[Noord]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Affairs-Manager-Leidinggevende-functie-tot-82k_1669927.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Voor and#233;and#233;n van mijn klanten in Noord-Holland ben ik met spoed op zoek naar een Senior Regulatory Affairs Manager. Het betreft een international georiand#235;nteerde farmaceutische organisatie waar een resultaatgerichte cultuur heerst. Dit betekent ook dat deze organisatie werknemers beloont die veel energie en ideeand#235;n investeren in deze organisatie. De functie betreft een global rol binnen een team waarin iedereen global verantwoordelijkheden heeft.De Senior Regulatory Affairs Manager gaat leiding geven aan een team van 3 Regulatory Affairs Managers. Daarnaast zal je in deze functie rapporteren aan de Head Regulatory Affairs. Naast het leidinggeven zal je je ook bezighouden met de registraties zelf en ervoor zorgen dat alle MAAand#146;s tijdig in orde zijn. Als Senior RA Manager ga je ook de strategie bepalen voor de commerciand#235;le producten. Vereisten:-Minimaal 7 jaar Regulatory Affairs ervaring in Biotech en/of Farmaceutische industrie-Msc in Farmaceutische, Biologische of Biotechnologische richting. -Vloeiend Nederlands en Engels in woord en geschrift. -Uitstekende communicatieve vaardigheden bij voorkeur in een global team-Proactief-AnalytischSalaris en Voorwaarden:-and#128; 57.000 and#150; and#128; 82.000 bruto per jaar, afhankelijk van ervaring-Bonus van maximaal 20% afhankelijk van bedrijf/individueel resultaat-LeaseautoReageren:Klinkt dit als een logische volgende stap in je carriere en voldoe je aan het profiel, upload dan nu je CV. Indien je vragen hebt, bel Robin Priems op +31 (0)20 522 15 77and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[MSL South UK]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA80A674BE4226514482579F5001FC115</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/MSL-South-UK_1669928.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[AccountabilitiesExcellent presentation and communication skills are essential as the role will require frequent presentations in a variety of settings. The person who fills this role will be expected to maintain and develop relationships with KOLs. They will represent Medical Affairs at national and international meetings, congresses and symposiums. Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice and reviewing submissions and formulary applications will all be part of the role. The MSL will also be expected to work with cross-functional colleagues in sales, marketing, market research, training, health economics, clinical operations and external affairs.If this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Information Associate  Danish or Norwegian Speaking  Pharma]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob902C092D6EA3D0DB482579F5001FC122</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Information-Associate-Danish-or-Norwegian-Speaking-Pharma_1669929.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Medical Information Associate - Danish or Norwegian Speaking - PharmaThis Global top 10 Pharmaceutical Company require an Associate Medical Information Specialist and#150; either Norwegian or Danish speaking, to join them immediately on initially a 9 month contract. The individual will be required to provide technical and medical information with high quality customer service. The AMIS will be responsible for researching and preparing responses for escalated medical inquiries as well as Scientific Response Documents related to one or two therapeutic areas. and#149; Research and respond to inquiries received via phone, email, internet or mail and#149; Document the inquiry and response according to relevant IG/SOP, and regulatory guidelines and#149; Responsible for identifying and recording, or triaging to responsible designee, adverse events and product complaints as well as processing fulfilment and#149; Exhibit broad knowledge of assigned therapeutic area and#149; Handle escalated MI inquiries from various sources and#149; Create and maintain European MI documents by ensuring responses are medically and scientifically accurate, timely, balanced, and meet customersand#146; needs. Fluent in English and Norwegian or Danish. and#149; Bachelors degree in a science/health-related field imperative (Pharmacy Degree Preferred) and#149; Some Pharmacy/Hospital experience preferred If you are interested in this position please contact Jessica Warden-Brown on 0207 758 7322 and send an up to date CV for consideration.  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ACCOUNT MANAGER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0752DB1D543096A8482579F5001FC12D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ACCOUNT-MANAGER_1669930.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I am currently recruiting on behalf of a Medical Communications agency for a an Account Manaage, You will be working on one of the largest accounts the company has with extensive client liaison and exposure. The agency offers a fantastic working environment with a vibrant and caring team. The successful candidate would be a key team member, handling direct client liaison. Attention to detail, proactivity and excellent communication skills are key. The candidate must be able to multi-task and naturally be able to keep a large amount of information and knowledge at finger tips. The Account Manager would be supported by the Account Director. For more information, please contact Rebecca Randles asap on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR MEDICAL WRITER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE7A044A40D41BAC482579F5001FC139</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-MEDICAL-WRITER_1669931.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A medical communications agency in London is looking to employ a senior medical writer to join their expanding agency. You will be responsible for the production of high quality medical copy that meets the clients objectives. This agency prides itself on working as a team and therefore you will be involved in business plans and strategies alongside promoting the company vision. Responsibilities involve:Quality of workWork in partnership with clientsManuscript and marketing productionAid the business team on development of proposals and pitchesInterpret and implement project brief from clients to team membersSkills:ProactiveTeam playerExcellent organisation skillsStrong scientific backgroundExcellent communication skillsFor more information contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical WriterSenior Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7A2F21287905E439482579F5001FC146</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Writer-Senior-Medical-Writer_1669932.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A top medical communications agency is looking to employ a medical writer or senior medical writer to join their expanding agency. You will be responsible for the production of high quality medical copy that meets the clients objectives. This agency prides itself on working as a team and therefore you will be involved in business plans and strategies alongside promoting the company vision. Responsibilities involve:Quality of workWork in partnership with clientsManuscript and marketing productionAid the business team on development of proposals and pitchesInterpret and implement project brief from clients to team membersEnsure all communication materials meet SOPsSkills:ProactiveTeam playerExcellent organisation skillsStrong scientific backgroundExcellent communication skillsFor more information contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Validation Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7F7A3655DCC29653482579F5001FC152</referencenumber>
<City><![CDATA[Adelaide]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Validation-Manager_1669933.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This global  company is a world leading pharmaceutical organisation. An exciting position has become available in the Quality/Validation team. The role involves  reporting to Director Biologics Quality Operations and supporting its internal biosimilar portfolio and third party BioServices product development  team. In this role you will be responsible for: - Providing Validation expertise to the site and managing Validation staff. - You will ensure that products moving through the development process and into pre-clinical/Phase 1 or later stage manufacture, are developed with appropriate Validation oversight for development.You will be integral in review and approval of subsequent transfers to an alternative company site, CMO or on site commercial manufacture.  You will be involved in maintaining the Validation system in compliance with current regulations and corporate requirements to support process scale up, transfer and regulatory submissions - Preparing  and /or approving SOPs, Validation documents , technical reports and  risk assessments  in support of internal  and external client requirements - Establishing a site Validation Master Plan and conducting validation activities including process, cleaning, equipment, facility/utility, together with oversight of analytical validation and automated systems validation. - Sound knowledge in validation principles, risk assessment tools and statistical tools.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality and Technical Support Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob07B6F752A36AA816482579F5001FC15F</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Quality-and-Technical-Support-Associate_1669934.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Join a multinational company in Sydney as a Junior associate and progress your career with excellent on-the-job training. and#60;band#62;This role involves:and#60;/band#62;1.Support on-going day to day QA and Technical activities.2.Manage the Stability and Validation Program at local CMOand#146;s.3.Manage the Product Quality Review Process.4.Manage the QI Secondary Inspection Process.5.Support the internal and external auditing program.and#60;band#62;Education, training, experienceand#60;/band#62;-Graduate Degree or Diploma in Science (e.g. Pharmacy, Chemistry, Microbiology, Engineering) -Admission (Member) to RACI, ASM or other relevant scientific association.-High level of Code of GxP knowledge and experience-3 years experience in a technical and/or quality or similar role in the Healthcare Industry.-Preferably 3rd party manufacturing background.and#60;band#62;You must ensure the following: and#60;/band#62;-That all product specifications, manufacturing and testing procedures are in line with the technical registration documentation filed at the TGA. -Manage the stability and validation program at local contract manufactures. and corporate requirement.-Manage the PQR schedule across local third party manufacturers and work with Senior Q and T Associate-Manage the secondary inspection against marketing authorizations process-Conduct release in SAP-Assist in the management of Certificate of Analysis (COAand#146;s).-Support internal and external auditing to maintain their ISO license .]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Customer Complaints Administrator]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE2BF72A8D4F0B02D482579F5001FC16B</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Customer-Complaints-Administrator_1669935.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Work for this multinational company and progress your career! This contract role requires someone with experience in customer complaints and experience in dealing with contract manufacturers. Experience at a multinational company is preferred! Management of customer complaints is a large part of the role and experience in this area is essential. You must maintain customer satisfaction and a GMP requirement as a sponsor and distributor of  therapeutic products.and#60;band#62;The Customer Complaints Administrator role exists to manage the following functions:and#60;/band#62;1. Manage customer complaints programs . a.Administer the local and global complaints databases.b.Pre-screening of the complaint sample.c.Coordinate the return of the samples back to the manufacturer for investigation.d.Coordinating the special biohazard sample returns process.e.Coordinate the response back to the customer once the investigation is complete.f.Follow-up delayed investigations.g.In conjunction with the Senior QA/Technical Associate, challenge the results of the investigations.h.Back-up for customer service to enter new complaints, contact customers for more information, and organizing replacements.-High level of Code of GMP knowledge and experience-Good presentation and report writing skills-Good project management skills-Excellent communication skills-High level of Computer literacy-Preferably 3rd party manufacturing background.-Ensure all Global KPIand#146;s are met.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[DirectorSenior Director, Clinical Operations]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB1C7A547FFB5F03482579F5001FC183</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-Senior-Director-Clinical-Operations_1669937.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Initiate and lead clinical study teams as clinical director. Responsible for the successful operations of all study teams to achieve the study objectives at the highest standards and on time and budget. Assist in protocol writing to completion, site selection, and working with internal managers/CRAand#146;s and CROand#146;s depending on the study to deliver patients, data, analysis, up until finalization of Clinical Study Report (CSR). All tasks and activities will be conducted full  compliance with regulatory requirements, GCP, good medical practice, and SOPand#146;s. Identifies program risks; proactively creates and implements mitigation strategies. Provide Sr. Management with necessary reports on progress and changes in scope, schedule and resources in a timely manner including preparation of presentations and documents to the Rand#38;D Strategy Committee (RDSC)  Works with internal team members in the development and implementation of compliance programs for Clinical Trials, including SOPand#146;s.   Travel approximately 20% of the time  Qualifications:10+ years managing clinical operations in a biotech/pharma company demonstrating a broad background in those environments. 5+ years of experience managing other clinical operations staff. Ability to manage the needs of multiple internal and external partners and deploy resources to meet those needs. Prior Experience managing oncology or hematology trials is a must.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. Principle Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob38CF872F64DEC8E0482579F5001FC193</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Principle-Engineer_1669938.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[-Perform standard engineering assignments, which are typically a significant portion of a larger project. -Utilize engineering tools to solve straightforward problems (e.g., FMEA, Finite Element Analysis, Process Modeling, Design of Experiments, SPC, software development). -Lead project teams as needed to accomplish project objectives. -Investigate new sources for raw materials or processes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance CPM Bavaria 6 months 5days 50% Onsite, 50 % Homebased]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4ACB6618CCA293CB482579F5001FC19F</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-CPM-Bavaria-6-months-5days-50-Onsite-50-Home-based_1669939.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Freelance Clinical Project Manager/ in Bavaria/ 6 months/ 5days/ 50% Onsite, 50 % Home-basedMy client is a large Pharmaceutical Company based in Bavaria who is looking for a Freelance Clinical Project Manager with experience in Non- Interventional Studies. Key Responsibilities:and#149;Responsible for conducting interventional (phaseIIIb, IV trials) and non Interventional studies (Registries, Post Authorization studies) in the CV therapeutic areaand#149;Leadership of a cross- functional international study teamand#149;Matrix Management of PAN European trials ensuring that all trial deliverables are met according to timelines, budget and resource requirementsand#149;Supervision of preparation and submission of all relevant study documents to authorities and regulatory bodies and their follow upand#149;Responsible for writing trial protocols, eCRF, project plans, trial reports, publicationsand#149;Management of study related Steering Committeeand#149;Daily Management of Vendorsand#149;Development of clinical outsourcing specifications with CROs and other 3rd partiesand#149;Contribution to the implementation of best practices and standards for trial management, including sharing lessons learnedand#149;Training of internal CRA regarding trial requirements and#149;Close collaboration with Medical Affairs with assuring that Study design meets the global medical strategy and#149;Representation of Clinical Operations in brand teamsand#149;Organisation and charing investigator meetings and team meetings Expertise and Complexity:and#149;University degree in medicine or natural sciences with a minimum of 5 years experience in the pharmaceutical industry, doctored preferred and#149;Minimum of 5 years experience in clinical research and international project management and#149;Thorough knowledge of Clinical Research Principles , ICH- GCP , EU regulations governing clinical trials, standard regulatory and clinical practices and current regulatory issues related to clinical research and#149;Thorough knowledge of Project Management tools and practicesand#149;Knowledge of Pharmaceutical business and international drug development and#149;Familiar with local regulations for NON and#150; Interventional studies within EUand#149;Fluent written and spoken English and German knowledge Salary/ Duration:and#149;Negotiableand#149;Start 01.06.2012and#149;End  01.12.2012 Apply now! Call Parminder Singh at Real Pharma on +49 69 264 89 8400 or send your CV to p.singh(at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QA Compliance Manager  12 Month Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob20346951BE55DC64482579F5001FC1AA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QA-Compliance-Manager-12-Month-Contract_1669940.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Role and Requirements: - Schedule internal GMP audits of all major departments and write reports following each audit. - Schedule outside GMP audits with corporate subsidiaries, vendors of Active Pharmaceutical Ingredients, Excipients, Packaging components, lebels and#38; inserts, recall houses, Contract Manufacturing facilities and outside laboratory test facilities around the globe and write report following each audit. - Extensive cGMP and Quality/compliance knowledge - Extensive internal and external auditing experience - Wide experience in the pharmaceutical industry - API auditing experience - Chemistry/pharmacist/biologics background would be very beneficial Strong emphasis on following soft skills is required - Positive attitude and willing to learn to acquire current knowledge by continuous learning process, since Compliance is a moving target. Good team player, tactful, understands systems, process within a short period. - Understands complex issues in a simple manner. An additional European language would be an advantage. Willing to travel 50% of the time is a must. Travel is not always confined to Europe, but should be willing to travel all over the globe. Potential to be away from home for up to 2 weeks at a time. This is an exciting opportunity for an excellent candidate to join a leading organisation. This is an immemdiate start - please contact Hemish Ilangaratne on 020 7758 7322 immediately and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Business Development Man. 5 Mon. near Munich Office based]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobACCF8CFD725882D5482579F5001FC1B7</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Business-Development-Man-5-Mon-near-Munich-Office-based_1669941.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a Pharmaceutical Client who is looking for a Freelance Business Development Manager with experience in creating contracts and Proposals for the CRO Business. Your support is needed to maintain the relationship with Key clients and also to acquire new Business in the Clinical area. Key Responsibilities: and#149; Responding to Customer requests  and#149; Providing Cost estimatesand#149; Drafting of contracts and change orders  and#149; Active customer Serviceand#149; Acquisition of new Clients Experience:and#149; 3 and#150; 5 years Business Development  and#149; Network of KOPand#180;s preferredand#149; Very strong interpersonal skills and#149; Fluent German and EnglishSalary/ Duration: and#149; Start: 01.06.2012 and#149; Duration: 5 monthsand#149; Location: Near Munichand#149; Rate: NegotiableIf you are interested in this position, please send me your updated CV to p.singh(at)realstaffing.com or give me a call on 069/ 264 89 8400. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Consulting Opportunities  London  Circa. £100K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDD110B081C0BA8B9482579F5001FC1C4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Consulting-Opportunities-London-Circa-and-amp-SHARP163100K_1669942.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[We are now working with a leading consultancy within the Brand Planning and commercial strategy sector they are now working on a number of roles to expand their UK division including a Head of EU Business and Senior Partner level roles.As a team they want team members who are dedicated to excellence in job performance, who truly enjoy communicating and working with others, and who can work at a very fast pace as part of dynamic and knowledgeable teams. We look for expertise in pharmaceutical and biotech strategy development, brand management, business development, clinical development, pricing and market access, commercial effectiveness, and other related practice areas. We are the premier specialized management consulting firm serving the pharmaceutical and biotech industries. As a consultancy they are able to compete with companies many times our size for the following reasons: They combine solid management consulting credentials with in-depth pharmaceutical and biotech expertise. Only hire talented people who can multi-task and work rapidly and effectively on cross-functional teams with senior management. They care about their people, clients and company. They have an ability to foster professional relationships at all levels.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Electrical Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob915592EDC495D120482579F5001FC1D0</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Electrical-Engineer_1669943.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for an Electrical Engineer to join a San Jose based medical device manufacturing company. This successful company is looking to bring on a leading member of their full time design team.Role: As an Electrical Engineer you will be responsible for the design and implementation and full cycle development of electro-mechanical infusion pump units through the complete product design cycle. Responsibilities include high speed digital design, power management, analog design and electric motor control, wired and wireless communication. This role also requires the ability to work cooperatively with a small team of engineers.Requirements:B.S. in Electrical Engineering or Computer Science5+ years of experience in hands-on design with analog and digital circuitsProven concept to launch development experience requiredStrong communication skills for a cross-functional roleSalary:and100-115k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Communications  UK & Ireland  Based South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob154A8D6BF5E94C9B482579F5001FC1E5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Head-of-Communications-UK-and-amp-SHARP38-Ireland-Based-South-East_1669944.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our client is a global science-based organisation that is focused in the fields of healthcare, nutrition and high-tech materials. They are leading innovators in a variety of healthcare sectors and within pharmaceuticals they are in the top 15 globally. The company is committed to clarity and excellence in its dialogue with key stakeholders both inside and outside of the organisation and as a result of a strategic initiative they wish to appoint a Head of Communications, UK and#38; Ireland based in their UK Headquarters in the South of England.Responsible for the UK and#38; Ireland Communications function, the role will be pivotal in driving the overall communications strategy and creating a centre of excellence that will enable the company to interact with its intermediaries in a variety of media formats.You will have a proven track record of professional communications within Life Sciences, coupled with strong media relations capabilities as part of a diverse public relations background. With the gravitas and ability to build strong relationships, you will be able to demonstrate proven leadership capabilities to lead and develop a communications team.For further information on this post please contact Sarra Gwilym on 0207 758 7311 or forward your CV following the details below.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Representative Neurologie(BerlinCottbusDresden)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE8DA30FDDF713BD8482579F5001FC1FA</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Representative-Neurologie-Berlin-Cottbus-Dresden_1641075.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Art der Tand#228;tigkeit: PermGehalt: nach VereinbarungOrt: BerlinUnser Klient ist  einer der erfolgreichsten Medizintechnik-Unternehmen aus Nordrhein-Westfalen, dessen Produkte weltweit Standards in Forschung und Industrie setzen. Ab sofort wir ein Sales Representative mit dem Schwerpunkt Neurologie gesucht.Sie haben schon erste Erfahrungen im Bereich der Neurologie sammeln kand#246;nnen?Ihre Aufgaben:and#149;die Betreuung der Bestandskunden im jeweiligen Gebietand#149;Ausbau des Kundenstamms durch Neukundenakquiseand#149;OP- Hospitationen Wir erwarten:and#149;Ein abgeschlossenes, idealerweise (medizin)technisches HochschulstudiumIdealerweise erste praktische Erfahrung in der Neurologie/ Intensivmedizinand#149;Eine hohe Kunden-Orientierung sowie Reisebereitschaftand#149;Gute Englischkenntnisseand#149;OP- Erfahrung im Bereich der NeurologieDes Weiteren zeichnen sich durch hohes Engagement, tadelloses Erscheinungsbild und ein zuvorkommendes Verhalten gegenand#252;ber den Kunden aus?Fand#252;hlen Sie sich angesprochen und sind Sie bereit fand#252;r eine aufregende Tand#228;tigkeit?Dann bewerben Sie sich umgehend. Fand#252;r weitere fragen steht Ihnen sehr gerne Herr and#214;ztand#252;rk zur Verfand#252;gung.Atilgan and#214;ztand#252;rk, Real Staffing GroupMedical DevicesTel.: 0049(0)69264898400E-Mail: a.oeztuerk(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QP Pharma  Sachkundige Person  Freiberufler  6 Monate  Berlin]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA870400DD04DB6F8482579F5001FC212</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QP-Pharma-Sachkundige-Person-Freiberufler-6-Monate-Berlin_1641076.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Einer meiner Mandanten ist eines mittelstand#228;ndisches Pharmaunternehmen, welches eine neue Filiale in Berlin erand#246;ffnet. Das Unternehmen sucht ab sofort fand#252;r den Standort in Berlin einen Freiberufler:and#60;band#62;QP Qualified Person nach and#167; 15 AMG and#60;/band#62;Ihr Profil:and#149; Abgeschlossenes Studium der Pharmazie and#149; Mehrere Jahre Erfahrung als Qualitand#228;tssicherheitsbeauftragter in der Pharmaindustrie and#149; Qualifizierung als Sachkundige Person nach and#167; 15 AMG (Qualified Person) and#149; Fachwissen and#252;ber nationale und internationale relevante Regularien cGMP and#149; Flieand#223;ende Deutsch und Englischkenntnisse  Ihre Aufgabenschwerpunkte:and#149; Sie and#252;bernehmen die Verantwortung fand#252;r die Einhaltung und Zertifizierung der GMP Anforderungenand#149; Sie sind der Ansprechpartner fand#252;r die kontinuierliche Verbesserung der Qualitand#228;tssicherungsaspekte and#149; Sie leiten Lieferantenaudits und nehmen an Kunden- und Behand#246;rdenaudits teiland#149; Sie sind fand#252;r die and#220;berwachung und Implementierung von CAPA zustand#228;ndigRATE: VERHANDELBARLOCATION: BERLINDAUER DES VERTRAGS: 6 MONATE STARTDATUM: 15. MAI  FLEXIBEL ARBEITZEITEN Dieses ist einer von vielen Interessanten Jobs, die ich meinen Kandidaten anbieten kann. Als Personalberater spezialisiert auf die Vermittlung von freiberuflichen Fach- und Fand#252;hrungskrand#228;ften im Bereich der pharmazeutischen Qualitand#228;tssicherung arbeite ich mit vielen Unternehmen in Deutschland, zusammen, die mich stand#228;ndig mit neuen interessanten Projekten versorgen. Falls ich Ihr Interesse wecken konnte bezand#252;glich des Jobs oder vielleicht im allgemeinen, zand#246;gern Sie bitte nicht, mich zu kontaktieren oder mir direkt Ihren aktuellen Lebenslauf zukommen zu lassen. Sie erreichen mich unter +49 (0) 69 264 89 8400 oder p.arroyave(at)realstaffing.com und ich wende mich an Ihnen so schnell wie mand#246;glich.Ich freue mich bald von Ihnen zu hand#246;ren. Selbstverstand#228;ndlich wird unser Kontakt vertraulich behandelt.Besten Dank im Voraus und Viele Grand#252;sse,Pedro Arroyave Recruiting ConsultantMedical Devices EngineeringReal Staffing Group GmbHTel: +(49) 69 264 898 400and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Clinical Project Manager mit dem Sponsor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEA345F07AF9CA552482579F5001FC21D</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Clinical-Project-Manager-mit-dem-Sponsor_1641077.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein unabhand#228;ngiges, forschendes und produzierendes pharmazeutisches Unternehmen mit 20 klinischen Studien in allen Therapiegebieten in Mittel- und Osteuropa.Ab sofort suche ich eine/n Senior Clinical Project Manager (Senior CPM), office based. Die Position ist nur als Festanstellung zu vergeben.Ihr Profil:+ abgeschlossenes Medizinstudium+ 5 Jahre Erfahrung im Project Management+ min. 2 Jahre Erfahrung als on site Clinical Research Associate (CRA)+ gute Kenntnisse mit nationalen und internationalen Regularien+ flieand#223;end Deutsch und EnglischBei weiteren Fragen stehe ich Ihnen gerne zur Verfand#252;gung.Beste Grand#252;and#223;e,Yuliyana KamenovaE-Mail: y.kamenova(at)realstaffing.comTel.:+49 264 898 400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Statistical Programming  Phase IIIUSMACambridge.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob19F79EBD6AF4497C482579F5001FC22A</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Contract-Statistical-Programming-Phase-III-US-MA-Cambridge_1641078.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[There are 2 potential contract positions with an interesting Global Pharmaceutical leader in the Cambridge area. This Senior Analyst, Statistical Programming supports statistical programming activities in the production of the analysis datasets, tables, listings, figures, electronic submission components, and complex ad hoc analyses. As a individual you are responsible for:*monitoring and meeting assigned study and program milestones.*requesting resources as needed. *leading a small team of support statistical programmers to accomplish tasks and communicate issues to senior management as necessary. *provides input to policy, operations, and capability building in Statistical Programming and Operations. *He/She develops and implements standard programming practices while also ensuring that they are employed across studies and programs.  I am looking for somebody with the following qualifications:- 5-10 years SAS Base programming, with 5-7 years using SAS STAT, GRAPH and MACRO-5-10 years relevant industry experience-5-10 years clinical trial experience-2 years clinical database experience-Excellent knowledge of drug development process-Knowledge of CDISC standards including SDTM and ADaM-Knowledge of drug submission requirements Education Bachelorand#146;s or Masters degree, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, IT.- The role is local based.-Hourly rate should be around 60-75 dollars an hour. If you are interested please let me know within a short notice and respond with your most recent resume.Best Regards,Jord]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Project Manager in Wien gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDD7DC5E64707CA3B482579F5001FC234</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Project-Manager-in-Wien-gesucht_1641079.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mit mehr als 600 Mitarbeiter gehand#246;rt mein Mandant zu den grand#246;and#223;ten forschenden und produzierenden Pharma- und Biotech-Unternehmen and#214;sterreichs. Momentan suche ich eine/n Clinical Project Manager (CPM), office based,  in einer Vollzeit/Festeanstellung.Ihr Profil:+ vorherige Erfahrung im Bereich Clinical Project Management, Clinical Study Management+ verschiedene Indikationsgebiete (Medical Devices ist vom Vorteil)+ Phasen I-III+ sehr gute ICG-GCP und FDA Kenntnisse+ fieand#223;end Deutsch und EnglischIch freue mich auf Ihre Bewerbung und bei weiteren Fragen stehe ich Ihnen gerne zur Verfand#252;gung.E-Mail: y.kamenova(at)realstaffing.comTel.: +49 69 264 898 400Mit freundlichen Grand#252;and#223;en,Yuliyana Kamenova and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior clinical research associate mit einem Pharmaunternehmen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD7F2212A9B21C4B8482579F5001FC241</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-clinical-research-associate-mit-einem-Pharmaunternehmen_1641080.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mit mehreren Standorten in Deutschland zand#228;hlt mein Kunde zu den erfolgreichsten Pharmaunternehmen weltweit. Weiterhin ist das Unternehmen auf verschiedene Therapiegebiete spezialisieret, darunter Kardiologie, Immunologie und Onkologie.Zur Zeit suche ich eine/n erfahrene/n Clinical research associate (CRA) mit dem folgenden Profil:+ naturwissenschaftlicher Hochschulabschluss+ min. 2 Jahre Industrieerfahrung im Bereich Onkologie+ sehr gute ICH-GCP Kenntnisse, Erfahrung in RA ist vom Vorteil+ Teamplayer und Organisationstalent+ flieand#223;end Englisch und DeutschBei weiteren Fragen stehe ich Ihnen gerne zur Verfand#252;gung. E-Mail: y.kamenova (at) realstaffing.comTel.:+49 69 264 898 400Mit freundlichen Grand#252;and#223;en,Yuliyana Kamenova  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Leiter QM und QMB für Medizinprodukte für Standort Berlin gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB970D5F29D5D8923482579F5001FC24E</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Leiter-QM-und-QMB-f-and-amp-SHARP252r-Medizinprodukte-f-and-amp-SHARP252r-Standort-Berlin-gesucht_1641081.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein Berliner Unternehmen, dass  langjand#228;hrige Erfahrung in der Herstellung von Implantaten und Instrumenten in der Endoprothetik und der Osteosynthese mitbringt sucht ab sofort einen Leiter QM.-and#220;berwachung der Sicherheit des Unternehmens sowie der Gesamtprozesse -Dokumentation des QM-System -Umsetzung der Anforderungen an die Prozesse des QM-Systems (ISO 13485)-Erstellung und Pflege des QM-Handbuchs, incl. VA, AA, FB-and#220;berwachung der Erstellung und Pflege von Produktarten -Prozessvalidierung in Kooperation mit Fertigung/Produktion -Messung und and#220;berwachung der Prozesse (Datenanalyse, Erstellen von Kennzahlen) -Zertifizierung der Produkte in Kooperation mit RA -Vorbereitung und Durchfand#252;hrung von internen und externen Audits in Kooperation mit RA -Termingerechte Bearbeitung von Reklamationen sowie die Veranlassung und Durchfand#252;hrung von Rand#252;ckrufaktionen-Einfand#252;hrung von Qualitand#228;ts-, Umwelt- und Arbeitssicherheits- Managementsystemen-Managementreport sowie Personalverantwortung-Nachweis der Maschinen- und Prozessfand#228;higkeit in Kooperation mit ProduktionIhre Qualifikation:-einschland#228;gige Berufserfahrung in den o.g. Bereichen-sehr gute Englischkenntnisse (in Wort und Schrift) -Beherrschung der gand#228;ngigen MS-Office Anwendungen-analytische Denkweise, Organisationsfand#228;higkeit, Analyse- und Problemland#246;sefand#228;higkeit und Sorgfalt bzw. Genauigkeit zeichnet -Kreativitand#228;t, Eigeninitiative, Engagement sowie Kommunikations- und Teamfand#228;higkeit Wenn Sie diese anspruchsvolle und spannende Aufgabe ansprechend finden und eine geeignetes Profil mitbringen, freue ich mich auf Ihre Bewerbungsunterlagen. a.wydra (at) realstaffing (dot) com / Agnes Wydra - +49 (0)69 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance and Compliance Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9E5F0FFC5744DF3482579F5001FC25A</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-and-Compliance-Manager_1641082.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading Pharmaceutical Services organisation is currently recruiting for a UK Quality and Compliance Manager on behalf of a blue chip pharmaceutical company. Responsible for a UK Team you will be responsible for a the UK GXP Audit plan of all services including, distribution, supply chain, document solutions, GMP Cleaning, Lab Services and facilities management. Key responsibilities include:Manage the UK Quality and Compliance team, to ensure that resources are appropriately applied and utilised, in the delivery of quality and compliance support to the operational teams.Manage the UK Quality and#38; Compliance team to aid the development and continuous improvement of the Global Quality Management System. Work with cross functional teams to investigate, root-causes analyse and implement corrective actions where GxP deficiencies are discovered.Present quality related topics to local business management. Perform investigations and special projects as required by senior management.Maintain communication with key business and client personnel.Provide guidance and assistance to Quality and Compliance staff.Conduct training in GxP and QMS topics, to the wider operations team.Assist the Business development teams in bidding / securing new business.If you are interested in this position you must have the following experience to relevant in your application:- Previous Management experience- Previous Pharmaceutical Audit Experience- Previous Experience in Quality Assurance The position is based in Hertfordshire and looking to pay up to and#163;45k plus benefits, if you wish to apply please send an updated CV to John Morkus or call 0207 758 7311 for further details.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager gesucht  Teilzeit]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob11D2180683BF5E27482579F5001FC267</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-gesucht-Teilzeit_1641083.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein junges und innovatives Unternehmen der Medizintechnik in Hessen ist aktuell auf der Suche nach Unterstand#252;tzung fand#252;r das Regulatory Affairs Team. Das Unternehmen zeichnet sich durch hohes Wachstumspotential aus, bietet einen zukunftssicheren Arbeitsplatz und sucht einen Teamplayer der sich neuen Herausforderungen stellt.Gesucht wird ein Mitarbeit, der 20 Stunden die Woche zulassungsrelevante Aufgaben bearbeitet. Hierzu zand#228;hlt die Erstellung der relevanten Dokumente, die Koordination und Einhaltung der notwendigen nationalen und internationalen Regularien, sowie die Betreuung des gesamten Zulassungsprozesses.Idealerweise haben Sie ein technisches Studium oder eine vergleichbare Ausbildung erfolgreich abgeschlossen, und bereits erste Erfahrungen in der praktischen Umsetzung und Pflege von Zulassungen gesammelt. Zu Ihren Qualifikationen zand#228;hlen sehr gute Englischkenntnisse sowie gute MS-Office-Kenntnisse. Ihr Profil wird durch Ihre Kommunikationsstand#228;rke, Durchsetzungsvermand#246;gen und Ihre Teamfand#228;higkeit abgerundet.Habe ich Ihr Interesse geweckt? Dann zand#246;gern Sie nicht, und kontaktieren mich!Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Associate (CRA)  3 month rolling contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDE6D59505BE07F27482579F5001FC273</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Research-Associate-CRA-3-month-rolling-contract_1641084.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This role is an office based role and the Global Pharma needs the candidate to have UK monitoring experience within Phase II/PhaseIII in the Oncology abnd Cardiovascular area. Travel expenses will be paid either for petrol or train cost when visiting sites. Global Site ManagementProtocol writingICH-GCP understandingDO NOT MISS OUT ON THIS OPPORTUNITYWe have referral schemes in place in your referral is placed. and#163;200 vouchers for a referral. KEYWORDS: CRA I, CRA II, CRA, Phase II, Phase III, Clinical Research Associate]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Statistical Programmer  SAS Programmierer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3F7A47D3FE77E91E482579F5001FC281</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Statistical-Programmer-SAS-Programmierer_1641085.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein weltweit fand#252;hrendes Pharmaunternehmen, welches seit Jahren eine ausgezeichnete Reputation in der Pharmaindustrie genieand#223;t, in mehr als 100 Land#228;ndern tand#228;tig ist und mehr als 10 Milliarden and#128; Umsatz jand#228;hrlich erzielt, sucht fand#252;r den Standort in Nordrhein-Westfalen einen Senior SAS Programmer / Senior Statistical Programmer Exzellente fachliche und persand#246;nliche Voraussetzungen sind meinem Kunden wichtig, aber vor allem wand#252;nscht sich mein Kunde Mitarbeiter, die Wertschand#228;tzung, Leistung und Engagement verbinden und aktiv Verantwortung and#252;bernehmen.Sie kand#246;nnen erwarten Hochmotiviertes und dynamisches Umfeldein aufstrebendes Arbeitsumfelderstklassige Entwicklungsmand#246;glichkeitenFlache HierarchieGgf. PersonalverantwortungAbwechslungsreiche Tand#228;tigkeiten Innovative HerausforderungenSie bringen mit:Mehrjand#228;hrige Berufserfahrung in der Programmierung mit SAS im PharmaumfeldPhase I und III ErfahrungKommunikationsfand#228;higkeiten im TeamKundenorientierer FokusFand#228;higkeit sowohl strategisch als auch operativ zu agierenSind Sie interessiert? Dann bewerben Sie sich jetzt online oder rufen Sie mich unter +49 (0) 69 264 89 8400 an. Gerne stehe ich Ihnen unter j.daake(at)realstaffing.com oder telefonisch zur Verfand#252;gung.-SAS Programming- Statistical Programmer- -klinische Studien- clinical- -klinische Prand#252;fungen and#150;SAS- programming- NRW -Nordrhein Westfalen -Kand#246;ln -Dortmund -Bochum -Wuppertal -Aachen -SAS Programmierung -SAS Programmierer  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Operations  CTAClinical Director Level  612 months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2630677525A2C1D9482579F5001FC28D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Operations-CTA-Clinical-Director-Level-6-12-months_1641086.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I am a recruitment specialist within the Clinical area dealing with such positions as Clinical Trial Associate, Clinical Research Associate, Clinical Project Manager, Clinical Trial Manager, Clinical Director. These are for contract positions for short and long term contracts for the Pharmaceutical, CRO, Biotech and NHS industry.I deal with 8 out of the top Pharmaceutical companies in the industry and have strong relationships built over time with colleagues and clients directly.I would be interested to discuss these opportunities with you in more detail and map out where you want your career to progress and discuss this with my existing clients.Please send across your CV and we can discuss opportunities further.If you are a Clinical Professional of any level looking into progressing to a new position, why not get in touch for a confidential discussion. We can provide you with a full honest look at what jobs are currently available and which employers would be interested in your skills. All enquiries are strictly confidential and our clinical team deal exclusively with the Clinical Research industry, speaking to decision-makers to keep abreast of the best new opportunities. KEYWORDS: CRA, CPM CTA, CTM. CSM, CLINICAL, PHASE I-IV, THERAPEUTICS, PHARMA, CRO, BIOTECH]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Data Manager Nähe Freiburg  Basel]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB750056F2050C1F0482579F5001FC29A</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Data-Manager-N-and-amp-SHARP228he-Freiburg-Basel_1641088.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, eine CRO ist ein unabhand#228;ngiges Auftragsforschungsunternehmen im Dreiland#228;ndereck Deutschland/Frankreich/Schweiz mit den Bereichen Klinische Forschung, Datenmanagement, Medical Drug Safety und Statistik und sucht zur Unterstand#252;tzung des Teams im Bereich Datenmanagement ab sofort einen erfahrenen Data Manager. Bei dieser Position ist Berufserfahrung in der klinischen Forschung wand#252;nschenswert. Ihnen wird ein spannendes und herausforderndes Aufgabengebiet in einem angenehmen Umfeld sowie sehr gute fachliche und persand#246;nliche Weiterbildungsmand#246;glichkeiten geboten.Ihre Aufgaben umfassen den:+ eigenstand#228;ndigen Aufbau sowie Validierung und and#220;berwachung von Studiendatenbanken + Programmierung von Abfragen+ Plausibilitand#228;tskontrollen+ Mergen von Daten+ Erstellung von Datenmand#228;ngellisten und Datennachfragen Sie sollten folgende Qualifikationen mitbringen:+ Hochschulabschluss in (Natur-) Wissenschaften, in einem medizinischen Fachbereich und/ oder eine langjand#228;hrige Berufserfahrung im Bereich Datenmanagement + Kenntnisse medizinischer Fachbegriffe + gute Kommunikations- und Teamfand#228;higkeit + fundierte Sprachkenntnisse in Deutsch und Englisch + Erfahrungen mit mehreren Datenbanken sind ein PlusKlingt dies nach der Herausforderung, nach der Sie suchen?Gerne stehe ich Ihnen fand#252;r Rand#252;ckfragen zu dieser, als auch zu anderen Stellen in diesem Fachbereich zur Verfand#252;gung. Julia Daake, Real Staffingj.daake(at)realstaffing.com +49 (0) 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SAS Analyst  SAS Devekoper  SAS Programmer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob23009D9E1D026FBD482579F5001FC2A7</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SAS-Analyst-SAS-Devekoper-SAS-Programmer_1641089.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is an expending CRO who is looking for a SAS Analyst/ SAS-Developer.The number of the employees has steadily grown since the day it was founded in all working areas and the organisation covers the following of those areas:Site management / monitoringDocument development / medical writing Data Management and StatisticPharmacokinetics The organisation operates in an international environment where you will be contributing to studies that truly affect global healthcare. Staff retention has been extremely high, due to outstanding working conditions, excellent remuneration package and remarkable team spirit.Job profile:+ Document - Development of SAS MACROS  1. Transformation of *.csv data downloaded from a EDC application to      reasonable (e.g. combination of all vitals information from several      CSV-files into one SAS dataset) SAS datasets.  2. Descriptive data analyses (generation of standard tables considering      ODS)- CDISC SDTM data export- Edit check programming- Maintenance and further development of VBA tools - Data Management- SAS trainer (in-house courses)- Development of MS ACCESS entry databasesThe organisation operates in an international environment, offers a progressive working environment where plenty of opportunity for further career development exists. For further information, please contact Julia Daake at Real Staffing j.daake(at)realstaffing.com or +49 (0) 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Quality Assurance]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCE19529F9D1F5CC7482579F5001FC2B4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Director-of-Quality-Assurance_1641091.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client a massive International pharmaceutical organisation is currently looking to recruit a new Associate Quality Director for the Global Quality Assurance Team within Research and Development Med Affairs.  As an Director you will provide auditing and Quality Assurance activities in order to assure that the systems, processes and performance comply with applicable laws, regulations, Standard Operating Procedures, protocols and guidelines, meet the overall business and manufacturing targets.Responsibilities:Provide Quality Assurance leadership and support within allocated Region, liaising with the Senior Director.Deputise for the Senior Director for delegated projects or during absenceEnsure sufficient Quality Assurance resource is available within allocated Region to cover planned auditing activitiesLine manage Quality Assurance personnel within allocated area, ensuring appropriate development and training of individualsProvide assistance with the maintenance of the global Quality Assurance SystemProvide assistance in assuring Senior Management of the effectiveness of the Quality Assurance Assist in the provision of QA review of Policies, SOPs, Working Guidelines and Associated Documents prior to approvalShould you have the required experience and are interested in this role please call John Morkus on 0207 758 7311 for an immediate and#38; confidential response on your CV.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Laborleiter in Nordhessen für Pharmaunternehmen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8F7488D73CE4B166482579F5001FC2C0</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Laborleiter-in-Nordhessen-f-and-amp-SHARP252r-Pharmaunternehmen_1641092.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Wollen Sie fand#252;r ein groand#223;es  Pharmaunternehmen in Nordhessen arbeiten? Das Unternehmen exportiert seine Produkte weltweit.Im Moment wird ein Laborleiter fand#252;r Nordhessen gesucht.   Ihre Aufgaben:- Prand#252;fung von Ausgangsstoffen  u. Arzneimittel- Verantwortlich fand#252;r die Freigabe von Ausgangsstoffen - Mand#246;glichkeit als Sachkundige Person weitergebildet zu werden und eingesetzt zu werden- Durchfand#252;hrung von Laborbezogenen Projekten- Mitarbeit bei der Auditierung von externen Prand#252;flaboratorienDie Anforderungen:Sie sollten ein abgeschlossenes Hochschulstudium der Pharmazie (Apotheker) haben. (evtl. mit Promotion) Des Weiteren sind fundierte Kenntnisse auf dem Gebiet der instrumentellen pharmazeutischen Analytik (HPLC/GC, IR/NIR/UV_DIS, Dissolution) wichtig. Laborabland#228;ufe und regulatorische Vorgaben in einem pharmazeutischen Unternehmen sind Ihnen bekannt.  Verhandlungssicheres Englisch und die Teamfand#228;higkeit wird ebenfalls vorausgesetzt. Sollten Sie diese Vorraussetzungen mitbringen, dann haben Sie die Chance sich gut weiterzuentwickeln. Bei weiteren Fragen kontaktieren Sie Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen an s.chaudhry(at)realstaffing.com. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior QA Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEF169D33205E497B482579F5001FC2CC</referencenumber>
<City><![CDATA[Melbourne]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-QA-Associate_1641093.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our client is highly successful pharmaceutical company looking for an experienced senior in quality assurance with a wide range of experience. This position involves assisting with internal and external quality systems and processes.  Key to this role is being capable of facilitating the organisations Quality Management Systems, ensuring that company products and processes adhere to TGA/FDA guidelines and other relevant regulations. and#60;band#62;The successful candidate will possess the following credentials:and#60;/band#62; -Tertiary qualifications in science or related discipline; -Experience in product release, deviation and customer complaints. -Prior quality assurance experience within the pharmaceutical industry;-Strong working knowledge of GMP manufacturing principles and guidelines;-Strong understanding of ISO 9001; -Technical understanding of processes involved in the manufacturing, packaging, testing and stability monitoring of pharmaceutical products.-Working knowledge of Quality standards and broad knowledge of Quality systems-Understanding of Quality Assurance policies and procedures, particularly in relationto compliance with regulatory, statutory matters and corporate guidelines.-Exceptional management skills.  This senior position is for experienced QA associates only looking to advance their level of responsibility and commitment.  Successful candidates will be contacted directly.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Drug Safety Physician (mw) gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9B4528F4F5FFDA6D482579F5001FC2DA</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Drug-Safety-Physician-m-w-gesucht_1641094.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Drug Safety Physician (m/w) gesuchtFand#252;r ein weltweit fand#252;hrendes, forschendes Pharmaunternehmen suche ich ab sofort einen and#60;band#62; Safety Physician (m/w) and#60;/band#62;!Aufgaben:and#149;In der Klinischen Entwicklung auf Augenhand#246;he als Persand#246;nlichkeit auftretenand#149;Schreiben von Risk-Management Pland#228;nenand#149;Unterstand#252;tzung bei Produkteinfand#252;hrungenand#149;Vertretung der gesamten Pharmakovigilanz Perspektiven im pre- und post-marketingFand#252;r diese Stelle sollten Sie folgende and#60;band#62; Eigenschaftenand#60;/band#62; nachweisen kand#246;nnen:and#149;Abschluss eines Medizinischen Studiums, eine Facharztausbildung ist von Vorteiland#149;Praktische Erfahrung in der Klinischen Forschungand#149;Fundierte Erfahung in der Pharmakovigilanzand#149;flieand#223;endes und sicheres Deutsch und Englisch in Wort und SchriftGerne erhalten Sie diskret und fachlich kompetent weitere Details. Ihr Ansprechpartner ist Hanna HolowatyTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, max. 1MB, and#252;ber den Online Bewerbungslink oder an and#60;band#62; h.holowaty(at)realstaffing.com and#60;/band#62;und rufen Sie mich an. Weiterhin besetze ich deutschlandweit weitere Positionen, als Festanstellungen, im Bereich der Pharmakovigilanz und im Medical Affairs. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete neue Perspektiven.Besuchen Sie mein XING Profil fand#252;r weitere Informationen.https://www.xing.com/profile/Hanna_Holowaty]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[GCP Compliance Specialist  San Francisco, CA  Biopharma]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA0B5E36A4F5CED35482579F5001FC2E7</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/GCP-Compliance-Specialist-San-Francisco-CA-Biopharma_1641095.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;GCP Compliance Specialistand#60;/band#62;The purpose of this position is to manage and lead GCP Audits to assure that all aspects of clinical trials conducted have been executed in compliance with applicable US FDA, ICH GCP Guidelines and other government and/or country specific regulations.This is a 6 month contract to permanent position.and#60;band#62;and60 - and80 per hour depending on experience.and#60;/band#62;and#149;Ensuring clinical trials are performed in accordance with applicable study protocols, and are in compliance with GCP and ICH guidelines. and#149;Conducting clinical document audits on Investigator Brochures, Clinical Protocols and Study Reports, Case Report Forms, Data Listings, and Informed Consents.and#149;Conduct Internal audits on the Trial Master Files.and#149;Conduct GCP compliance audits of Investigator sites and Vendor facilities in accordance with annual Audit Plans. and#149;Conduct internal department audits to ensure compliance with Department Guidelines and Procedures, and GCP and ICH guidelines. and#149;Provide guidance on existing and new GCP regulations to clinical teams.and#149;Represent the CQA department on the clinical department teams.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Program Manager Managed Care Marketing]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD7CB121392CEC0B0482579F5001FC2F4</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Program-Manager-Managed-Care-Marketing_1641096.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A thriving and innovated Diagnostics company located in the San Francisco Bay Area is currently seeking a Program Manager of Managed Care Marketing to add to their close knit and expert team. This privately held firm specializes in a cardiovascular diagnostics test, which is the first of its kind and currently FDA cleared. The Role: -As the Manager of Managed Care Marketing you will be responsible for developing and implementing strategies in efforts to support payer relations, coding, and coverage -Private payer market research- payer roundtables/ad boards, synthesis of data and summarizing results for internal and external use-Supporting HEOR models into payer relations tools for use in discussions with commercial payer medical directors-Working cross functionally with clinical, market access, field reimbursement team]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Clinical Operations  Ohio]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD11223D1A3EC9522482579F5001FC301</referencenumber>
<City><![CDATA[Ohio]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-of-Clinical-Operations-Ohio_1641097.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Requirements:Education:Masters or Doctoral degree or equivalent in a scientific discipline Experience: Ten or more years of clinical research experience with five or more years of experience in the development and#38; management of clinical operations function and direct management of staff in a pharmaceutical and/or biotechnology environment; previous field CRA experience desired; the final title will be commensurate with the candidates experience Experience with international trials (including regulatory submissions, CMC, clinical operations)Proven excellence in operational strategy; experience with developing, implementing, and measuring the impact of clinical operations tools across multiple projects Experience developing and implementing functional and cross-functional SOPs and processess Knowledge, Skills, and Abilities:Thorough knowledge of FDA regulatory requirements and ICH/GCP guidelines essential Demonstrated proficiency in the implementation, monitoring and management of clinical trials including clinical supply and document control functions, timelines and budgets with all phases of development (including regulatory processes and contract hurdles) Demonstrated ability to build, coach, motivate and supervise a high performing team in a growing company, including ability to clarify roles and responsibilities Ability to establish excellent internal and external relationships; including alliance partners and vendors  Essential Duties and Responsibilities:Participate in strategic planning activities and translate strategic decisions into operational plans Assess organizational needs and build a scalable infrastructure to support ATM Clinical programs. Ensure adequate resources for clinical operations, and participate or support, as needed, including operational plans, tactical execution, protocol preparation, report writing, regulatory submissions, etc. Design and maintain operational processes and systems to allow cost- and time- effective execution of high-quality clinical studies in accordance with all applicable regulations. and#38;#9702;Ensure the appropriate implementation of clinical infrastructure within ATM including SOPs, policies and cross-functional communication and interactionand#38;#9702;Ensure consistency of operational approach across multiple clinical studies and development programsProvide operational input into integrated development plans and study protocols, as requiredDirect clinical program implementation to meet program timelinesLead clinical projects (as Clinical Project Leader) as requiredAssist in development of US cost estimates and budgets for clinical trialsManage staff within ATM Clinical Operations; and provide guidance to ATM Clinical Project Leaders and CRAs in analyzing and resolving issues relating to study design,  protocol execution and compliance Manage the functional area budgets; provide senior management with necessary updates on progress and changes in scope, schedule, and resources in a timely manner.Must be available for domestic and international travel up to 15%, dependent upon progress of programsand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director of Biostatistics  $150,000 to $170,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob68D83D00E5B8F725482579F5001FC310</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Associate-Director-of-Biostatistics-$150000-to-$170000_1641098.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The Associate Director Biostatistics acts as fully independent global statistical lead (GSTATL), representing Data Science in Core Teams. He/she may be responsible for one or for multiple global or local drug projects within the same indication / therapeutic area. He/she leads large and/or complex projects, interacts with regulatory authorities and key opinion leaders, supervises other statisticians providing support to the projects and is accountable for the statistical soundness of ALL statistical input and deliverables for the assigned projects. Provides consultancy to other project teams and other GSTATLs in areas of expertise. He/she is expected to complete these tasks with very minimal supervision, appropriately and pro-actively seeking line management intervention where needed to ensure successful outcome, e.g. with respect to project resource requirements or key strategic functional issues. RequirementsM.S. or Ph.D. in statistics or equivalentMinimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the big picture.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressureand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager of Medical Writing New Jersey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF46F3832542DCDBA482579F5001FC328</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Manager-of-Medical-Writing-New-Jersey_1641103.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A small pharmaceutical company boasting a robust pipeline is seeking an experienced Senior Medical Writing Manager, responsible for hands-on regulatory writing.  Salary is highly competitive with up to and140k and 20% bonus!  The management team is looking to add to upper management in medical writing - this position reports to Director and also there is no direct report responsibilities.-Write protocols, IBs, CSRs, Clinical sections of the CTD (2.5, 2.7.3, 2.7.4), integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses-Hands-on writing on all documents as well as supervision of work performed by CRO/Consultant writers-Critically review documents produced by external writers-Assist Clinical Study Managers with managing documents through review processRequirements:-BS in scientific field, MS/PhD Preferred-5-10 years of regulatory writing experience-Excellent interpersonal, cultural and communication skills-Experience with diagnostic imaging agents preferred-Documentum proficiency or something similarThis company offers excellent compensation and growth opportunities as well as great benefits.  Do not miss this opportunity to be a leader and innovator in the medical writing field!Send Resumes to Dandan Zhu at Real Pharma, contact me today at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director Medical Writing  Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA8ACF9804894D803482579F5001FC334</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Associate-Director-Medical-Writing-Medical-Writer_1641104.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Small international pharmaceutical company is seeking an Associate Director to join the medical writing group and lead the in-house writers as well as the contract writers.  This is an excellent opportunity to be an important member of this close-knit group that will offer the chance to participate heavily in life cycle management.  Salary is up to and140k and there will be 20% bonus! Position is located in New Jersey or Massachusetts.Responsibilities:-Prepare documents for regulatory submissions such as NDAs, INDs, CSRs, IBs, ISS, ISE, COs, RMP, briefing books, summaries of efficacy and safety, dossiers, etc-Managing contractors and mentoring in-house writers -Work closely across functional teams to accomplish goals within the set deadlines-Reviews DPP and SAP as needed-Prepare budgets, establishes target dates for completion of assignments, establishes SOPs and quality standards for documentsRequirements:-6-8 years of solid medical writing experience in submission documents-Submission or lead writer experience on complex documents REQUIRED-Minimum of BS, advanced degree such as MS, PhD or Pharm D or BSN is preferred-Excellent communication skills This company offers excellent bonuses, quarterly rewards, strong benefits package, and relocation packages are provided as well.  Do not miss this great chance to make a difference and be a treasured member of the team!Apply today and send resumes to Dandan Zhu at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Medical Writer Massachusetts]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob40FB4EC96F4FF01B482579F5001FC341</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Principal-Medical-Writer-Massachusetts_1641105.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Exciting in-house medical writing opportunity located in Cambridge, MA seeks an independent, experienced professional to lead the writing effort and work with senior management to set up document standards.  Salary is highly attractive at up to and140k+bonus. There will be lots of submissions coming through and significant chances to accelerate your career!We are searching for experienced writers specializing in Clinical Study Protocols, Clinical Study Protocol Amendments, Clinical Study Reports, Investigator brochures, Clinical Summaries and other documents, as needed.Main job responsibilities include:and#149;Working with the clinical team and providing guidance for format and organization of clinical filingsand#149;Write CSRs, protocols, IBs, ISS, ISE, NDA, BLA and IND submissionsand#149;Help to coordinate the efforts of the consultant writers and vendors.Requirements/Skills:and#149;More than 6 years of medical writing experienceand#149;Minimum of B.S. degreeand#149;Experience in leading NDA/BLA filings, EMEA filing experience a plusand#149;Great team player with some management experienceand#149;Effective relationship and communication skillsWe offer extremely competitive compensation and generous benefits package including stock incentives.  Donand#146;t miss this opportunity to grow in a nurturing, dynamic, collaborative and energizing company environment!  Send Resumes to Dandan Zhu at Real Pharma, contact me today at 212-707-8499]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Control (QC) Inspection Technician]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob86FD9214A3E31A8A482579F5001FC34E</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Control-QC-Inspection-Technician_1641106.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Quality Control (QC) Inspection Technicianand#60;/band#62;and#60;/uand#62;A medical device company in Mountain View, CA area is looking for a Quality Control (QC) Inspection Technician to join their team.  This is an urgent position and we are looking to identify someone immediately.  You will be responsible for interpreting specifications, microvision, optical comparitors, micrometers, and calipers.and#60;band#62;Quality Control (QC) Inspection Technician Requirements:and#60;/band#62;- A minimum of 2 years of Quality Control experience within the Medical Device industry- Experience interpreting specifications, microvision, optical comparitors, micrometers, and calipers.and#60;band#62;If you are interested in applying for this role, please respond to this advert immediately with an updated version of your resume.  and#60;/band#62;]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ProduktmanagerTomografiegeräte]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0DD497FB0ED28806482579F5001FC35C</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ProduktmanagerTomografieger-and-amp-SHARP228te_1641107.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Art der Tand#228;tigkeit: PermGehalt: 70000Ort: HessenMein Kunde ist seit and#252;ber 50 Jahren ein Spezialist im Bereich der dimensionalen Messtechnik und ist international tand#228;tig. Im Zuge des stetigen Wachstumspfades wird momentan ein Produktmanager gesucht. Als Produktmanager erwarten Sie u.a. folgende Aufgaben:and#149;Enge Zusammenarbeit mit der Entwicklungsabteilung bei der Erstellung von Produktkonzepten and#149;Ausarbeitung von Vertriebsstrategien und deren Optimierungand#149;Direkter Kontakt zu Key Accounts (Groand#223;kunden, Hochschulen)and#149;Markt- und WettbewerbsanalyseHierfand#252;r bringen Sie folgende Eigenschaften und Qualifikationen mitbringen:and#149;Mehrere Jahre Erfahrung im Produktmanagement von hochwertigen Investitionsgand#252;ternand#149;Eine Promotion oder ein sehr guter Studienabschluss als Physiker oder Ingenieurand#149;Kommunikationsstand#228;rke und Durchsetzungsvermand#246;genFand#252;hlen Sie sich angesprochen und sind Sie bereit fand#252;r eine aufregende Tand#228;tigkeit?Dann bewerben Sie sich umgehend. Fand#252;r weitere fragen steht Ihnen sehr gerne Herr and#214;ztand#252;rk zur Verfand#252;gung.Atilgan and#214;ztand#252;rk, Real Staffing GroupMedical DevicesTel.: 0049(0)69264898400E-Mail: a.oeztuerk(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Experte iin der Drug Safety (mw) in Bayern gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAD7F917BFEC9EC31482579F5001FC367</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Experte-iin-der-Drug-Safety-m-w-in-Bayern-gesucht_1641108.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein forschendes  Pharmaunternehmen aus dem Raum Bayern und ich suche einen and#130;Experten in der Drug Safety (m/w).Das Aufgabengebiet:and#149;Bewertung und Meldung des Nebenwirkungsspektrumsand#149;Signal Detectionand#149;Kommunikation und Abstimmen mit anderen Bereichen wie dem Global Headquarter, dem Clinical Bereich oder dem Regulatory Bereichand#149;medizinische Bearbeitung von Einzelfallberichtenand#149;Erstellung von narratives und anderen behand#246;rdlichen BerichtenWas mand#252;ssen Sie mitbringen?and#149;Abgeschlossenes Studium der Humanmedizin oder der Pharmazieand#149;Als Naturwissenschaftler bringen Sie fundierte und deutliche Erfahrung in der Pharmakovigilanz mitand#149;Selbststand#228;ndigkeit, eine schnelle Auffassungsgabe und Organisationstalentand#149;Ein ausgeprand#228;gtes Kommunikationsvermand#246;gen und Teamfand#228;higkeitand#149;sehr gute Deutsch- sowie EnglischkenntnisseNa, wie klingt das fand#252;r Sie? Gut? Dann freuen wir uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Frau Hanna Holowaty (h.holowaty(at)realstaffing.com) wenden.Real Pharma berand#228;t Unternehmen weltweit bei der Besetzung ihrer Positionen im Pharmabereich. Wir bieten auand#223;ergewand#246;hnliche Jobmand#246;glichkeiten fand#252;r talentierte Fachkrand#228;fte. Profitieren auch Sie von unserem qualifizierten Netzwerk und unserem Knowhow.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent Document Control Specialist San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob119D199B81D7D9CF482579F5001FC37E</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-Document-Control-Specialist-San-Diego_1641109.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has an urgen need for a Document Control Specialist for His QC department. This candidate must have experience in both QA and QC.Requirements:-Must be able to multy task and where different hats-experience in both QA/QC-document control-FDA knowledge-ISO, SOPs, Quality Management Systems- must be able to travel-some international travel -good team work skills, organizationThis is an excellent opportunity with a massively expanding company with new innovative products. Please respond ASAP by sending your resume if interestedKeywords: DOCUMENT CONTROL, FDA,SOP,ISO, BIOTECH,PHARMACEUTICAL, QA, QUALITY ASSURANCE, QC, QUALITY CONTROL]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principle Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDAA008EC2D84A3D1482579F5001FC38A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Principle-Medical-Writer_1641110.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you a Senior Medical Writer with experience, skills and application to progress to Principal Medical Writer? If so, we want to hear from you!Due to continued growth my client is looking to employ a Senior Medical Writer to join their strong editorial team. This is a fantastic opportunity to fast track your career to a Principal Medical Writer or Team Leader through supporting the developments on new and existing accounts.Skills/Experience:- Agency exposure as a Medical Writer- Development of abstracts, posters, primary and secondary manuscripts, review articles- Client liaison skills- Mentoring and reviewing the work of junior writers- A broad range of therapeutic knowledgeMy client will offer a competitive salary and benefits package for the right candidate.For more information, please contact Rebecca Randles on 0207 758 7311]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent  QC Analyst  San Diego; Enzyme exp]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob041FDC310B79FDD0482579F5001FC397</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-QC-Analyst-San-Diego-Enzyme-exp_1641111.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[As QC Analyst, the candidate would be responsible for conducting quality control routine and non-routine analysis of raw materials, in process, and finished formulation enzyme products according to standard operating procedures.  Job scope includes performing new method development, method improvements and validation of enzyme activity determination or supporting assays.Critical Competencies:and#149;         Conducts microbiological and analytical analyses according to standard operating procedures (SOPs)and#149;         Reviews results for compliance to specifications and reports deviationsand#149;         Analyzes data and prepares reports, upon requestand#149;         Prepares and revises SOPs and test methods, as requiredand#149;         Conducts necessary maintenance and calibration of lab equipment and#149;         Conducts problem solving on analytical and instrument issues, as requiredand#149;         Applies knowledge of good laboratory practices on a daily basisand#149;         Performs method transfer to and training of toll manufacturing personneland#149;         Travel will be required and can be as much as 25% of time Education/Experience:BS in Biological Sciences or related field and 1-2 years experience working with enzymes or proteins and running colorimetric enzyme assays preferred. General molecular biology and biochemistry laboratory techniques, including:  gel electrophoresis, spectrophotometry, a basic understanding of enzyme-catalyzed reactions and kinetics is required. Any analytical experience such as HPLC would be advantageous. Bilingual in English and Spanish is a plusThis is an extremely attractive offer that will not be available for long; Interviews next week. Please send resume if you are interested.Keywords: QC, QUALITY CONTROL, PCR, HPLC, ELECROPHORESIS, ASSAYS, ENZYME ASSAYS, SPANISH]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Account Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBA3EE669E156F313482579F5001FC3A4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Account-Manager_1641112.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[As the Head of Medical communications at Real Pharma I am currently recruiting on behalf of a medical communications agency for an Account Manager. As Account Manager the role would result in working predominantly on oncology accounts and reporting into the Account Directors. As AM some of your key responsibilities will include:and#149;  Managing the financial aspects of their designated projects and#149; Liaising with clientsand#149; Mentoring and possibly being a line manager for an Account ExecutiveIf you are interested in this opportunity you must:and#149; Have a degree in a relevant subject (e.g. life science) and#149; At least three years agency or relevant client side/industry experienceand#149; Mentoring/training experience and#149; Have experience in overall account management and project management, budget preparation, financial management, client liaison and event management, organic business growthIf you wish to apply for the position please send an updated CV or email to r.randles(a)realstaffing.com. The position is based in London and is looking to pay between and#163;30,000-and#163;40,000Keywords: Account Manager,  Med comms, Medical Communications]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Editor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob044E0A95D8EF04B3482579F5001FC3B0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Editor_1641113.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Medical Communications agency in London is now seeking a Medical Editor or Senior Editor to join their growing business. Role and Responsibilities The Medical Editor/Senior Editor is responsible for QC/editing and proofing of all types of material including: Manuscripts/first drafts written in Word by Medical Writers (MW) PowerPoint (PPT) presentations Artworked items Proposals/pitch presentations Corporate marketing materials Websites This agency is not a publications based agency. They have a wide spectrum of services. Materials need to be highly designed and patient friendly.The Medical Editor/Senior Editor should be adept at interpreting and incorporating client comments and working in conjunction with Medical Writers. For more information, contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Representative in Medical Devices mw]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA4F7BB32D502DCB5482579F5001FC3BB</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Representative-in-Medical-Devices-m-w_1641114.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global healthcare products company, searching for a Sales Representative for the segment and#150; Neurovascular.The vacancy entails you to perform the following tasks:and#149;Active within field salesand#149;Client consultingand#149;Client additionand#149;Overall business developmentand#149;Attending and presenting at medical device specific fairsand#149;Presenting the company at eventsYour Profile:and#149;Several years sales experience in Cathlab and#149;Experience in interventional neurovascular environment preferred, thorough understanding of selling in a hospital environment and#149;A successful completion of a business-related Degree, or numerous years experience in the field of salesand#149;Several years experience in the overall market concerning and#147;Medical Devicesand#148;and#149;Follow a confident worth ethicand#149;Strong communication skillsand#149;Experience and knowledge of medical device products and industryAdditionally, the position brings with it an attractive salary package.Do you recognise yourself? Then do not hesitate to send me your CV, to get further details. Your contact person is Simone Schaefer, email:  s.schaefer(at)realstaffing.com. Contact number: +49 (0) 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD010A069D8F0725C482579F5001FC3C8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Writer_1641115.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Medical Education Agency is seeking to employ a MEDICAL WRITER to join their team in the South East.As a MEDICAL WRITER you will be responsible for writing and delivering scientific information that meets the clients brief on time and in budget. You must be adaptable to learn about new therapeutic areas and be able to relay this confidently across to clients. A Medical Writer will be able to write high quality, scientifically accurate and grammatically correct text in line with the requirement of the client and at a level that is appropriate for the final audience. Documentations will include; manuscripts, print publications, multimedia and website. Having recently won a number of pitches for existing and new business they are seeking to grow their team by employing a medical writer.This is an opportunity not to be missed, so if you have a life science degree and medical communications experience, then please do not hesitate to contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8003CB76309242FF482579F5001FC3D4</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Writer_1641116.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Medical Communications Agency in Central London is currently seeking to employ a MEDICAL WRITER to join their growing team.As a MEDICAL WRITER you will be responsible for writing and delivering scientific information that meets the clients brief on time and in budget. You must be adaptable to learn about new therapeutic areas and be able to relay this confidently across to clients. A Medical Writer will be able to write high quality, scientifically accurate and grammatically correct text in line with the requirement of the client and at a level that is appropriate for the final audience. Documentations will include; manuscripts, print publications, multimedia and website.This is an opportunity not to be missed, so if you have a life science degree and medical communications experience, then please do not hesitate to contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent  Senior Supplier Quality Engineer  San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3C4ABC79F77C3286482579F5001FC3E0</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-Senior-Supplier-Quality-Engineer-San-Diego_1641117.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has an Urgent need for a Senior Supplier Quality Engineer who would be willing to make international trips on the occasion with the following requirements:-5-6 yrs experience- experience in Supplier Development/ Certification-needs to be able to work independently and have leadership skills- management exp (6-8 yrs)- exp. With  PCBAs, circuit boards, molding, injections, plastics-good communication skills- will be communicating with suppliers, internal customers- help remedy key issues across production cells- six sigma -ASQ cert-supplied evaluations-med device or specialized PCBA background- automotive experience is a plus-** customer service and communication- will be dealing with foreign suppliers]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Ingenieur (Medizintechnik) Baden Württemberg]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob551A4113058B8535482579F5001FC3EC</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Ingenieur-Medizintechnik-Baden-W-and-amp-SHARP252rttemberg_1641118.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r einen gesunden Mittelstand#228;ndler aus der Medizintechnik Branche suche ich einen Quality Ingenieur. Das Unternehmen ist international ausgerichtet und hebt sich mit innovativ entwickelten Produkten vom Markt ab. Die Herstellung ist am Standort. Hervorzuheben ist der attraktive Standort, beste Arbeitsbedingungen und Atmosphand#228;re sowie ein  attraktives Gehaltspaket.Folgendes erwartet Sie:and#149;Validierung von Anlagen und Prozessenand#149;Erfahrungen im Bereich Qualitand#228;tsmanagementand#149;DokumentationFolgendes bringen Sie mit:and#149;Berufserfahrung in der Medizintechnikand#149;Stark technischer Background wie Ingenieur Studium oder vergleichbare Qualifikationand#149;Kenntnisse der erforderlichen Gesetzte und Regularien wie ISO 13485, ISO 9001, FDA usw..and#149;EnglischkenntnisseGerne erhalten Sie diskret und fachlich kompetent weitere Details. Ihr Ansprechpartner ist Simone LeberTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, and#252;ber den Online Bewerbungslink oder an and#60;band#62; s.leber(at)realstaffing.com and#60;/band#62; und rufen Sie mich an. Weiterhin besetze ich weitere spannende Positionen im Bereich Qualitand#228;t in der Medizintechnik. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete  Ihnen neue Perspektiven. Besuchen Sie mein X I N G Profil fand#252;r weitere Informationen.https://www.xing.com/profile/Simone_Leber and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Vertriebsleiter Deutschland]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBE4917DD50B7F19B482579F5001FC3F8</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Vertriebsleiter-Deutschland_1641119.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Art der Tand#228;tigkeit: PermGehalt: 60000-90000Ort: Hessen, (Homeoffice)Mein Kunde ist seit and#252;ber 50 Jahren ein Spezialist im Bereich der dimensionalen Messtechnik und ist international tand#228;tig. Im Zuge einer geregelten Altersnachfolge wird ein Vertriebsleiter Deutschland gesucht. Als Vertriebsleiter erwarten Sie u.a. folgende Aufgaben:and#149;Nationaler Vertrieb und Auftrags Verhandlungand#149;Markt und Wettbewerbsanalyseand#149;Kundenpflege und Entwicklung von Vertriebsstrukturen Hierfand#252;r bringen Sie folgende Eigenschaften und Qualifikationen mitbringen:and#149;Fand#252;hrungspersand#246;nlichkeit gepaart mit einem technischen  Hochschulabschlussand#149;Interesse an High- Tech Produkten und Erfahrung im Investitionsgand#252;tergeschand#228;ftand#149;Durchsetzungsvermand#246;gen, Belastbarkeit und eigenstand#228;ndiges ArbeitenFand#252;hlen Sie sich angesprochen und sind Sie bereit fand#252;r eine aufregende Tand#228;tigkeit?Dann bewerben Sie sich umgehend. Fand#252;r weitere fragen steht Ihnen sehr gerne Herr and#214;ztand#252;rk zur Verfand#252;gung.Atilgan and#214;ztand#252;rk, Real Staffing GroupMedical DevicesTel.: 0049(0)69264898400E-Mail: a.oeztuerk(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales Manager mw, Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob80359F50D3976DBF482579F5001FC405</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-Manager-m-w-Medical-Devices_1641121.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is an industrial enterprise, specialising in the sector of Ophthalmology of medical devices and Ophthalmic Optics. Currently they are seeking a:Product Manager m/wThe role encompasses the realisation, planning and structuring of marketing concepts and to develop continual improvements to their product line. The position also requires you to hold and present conferences/seminars, as well as to attend medical device specific fairs. The position is therefore an interesting combination of business development, brand management, sales support and overall constant market analysing. The Profile:and#149;Successful completion of a Marketing/Business Management Degreeand#149;Several years experience in the areas of: ophthalmologyand#149;Several years experience in field sales and Key Account Managementand#149;Team leading know-how and#149;Strong communication skills which allows you to gain the interest of and convince your relevant business partnersand#149;Team leading ability, responsibility seeking, strong negotiation skills and performing with a confident work ethicand#149;Familiarity with  MS-OfficeIf this vacancy sounds appealing to you, then please contact Simone Schaefer at Real Pharma Frankfurt for more information. Tel: +49 (0) 69 264 89 8400/ Email: s.schaefer(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager Regulatory Affairs  Leidinggevende functie  tot 80k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob13F7CC8BAEC6220D482579F5001FC412</referencenumber>
<City><![CDATA[Zuid]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Manager-Regulatory-Affairs-Leidinggevende-functie-tot-80k_1641122.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Deze organisatie in Zuid-Holland is op zoek naar een Regulatory Affairs Manager. Deze positie is vrij gekomen door de groei die deze organisatie doormaakt. Deze organisatie laat zich kenmerken door haar generieke producten zoals zalven, crand#232;mes, drankjes etc. Hiervoor verzorgt deze organisatie de loonproductie voor diverse grote farmaceuten. Ook draagt deze organisatie zorg voor magistrale bereidingen en productie voor clinical trials.Als Regulatory Affairs Manager ben je eindverantwoordelijk voor de afdeling. Daarnaast stuur je 3 Regulatory Affairs Professionals aan. Ook ga je je inhoudelijk bezighouden met registraties van de producten die binnen deze onderneming worden geproduceerd. Samenstellen en indienen van registraties files zijn ook onderdeel van deze functie. Uiteraard sta je ook in contact met zowel nationale als internationale autoriteiten.  Dus heb jij:- Minimaal 2-3 jaar ervaring als RA Manager in een farmaceutische organisatie-Minimaal 3-4 jaar ervaring met samenstellen/indienen registratie files-Universitaire opleiding in Farma, Life Science of Chemie - Aantoonbare leidinggevende ervaring- Goede kennis van Nederlandse en Europese registraties - Sterke communicatieve vaardigheden, zowel mondeling als schriftelijk - Goede kennis van de Nederlandse en Engelse taal in woord en geschriftVoorwaarden:-Salaris tussen and#128;65.000- and#128;80.000 bruto per jaar-Premie vrij pensioen-Bonus and#150; afhankelijk van bedrijfs-/individuele prestatiesKlinkt dit als de ideale volgende stap in je carriand#232;re? Stuur dan je meest recente CV Real Staffing Group of bel 020 522 15 77 en vraag naar Robin Priems.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Account Manager  Bayern  Pharma  tolle Einstiegsposition]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7FF8194EC5BE913F482579F5001FC41D</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Account-Manager-Bayern-Pharma-and-amp-SHARP150-tolle-Einstiegsposition_1641123.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist seit Jahrzehnten im Einsatz fand#252;r die Gesundheit der Menschen.Um seine Kunden stets die beste Unterstand#252;tzung bieten zu kand#246;nnen, wird ein Mitarbeiter fand#252;r den Vertrieb gesucht.Sie betreuen Vertriebspartner und sind mitverantwortlich fand#252;r die  Planung, Durchfand#252;hrung sowie Kontrolle der Umsatz- und Absatzdaten der Produkte. Sie and#252;bernehmen eigenstand#228;ndig den Aufbau des Kundenstamms und gestalten das Beziehungsmanagement fand#252;r die Kundenbindung mit den Vertriebspartnern.Hierfand#252;r sollten Sie einen naturwissenschaftlichen oder betriebswirtschaftlichen Abschluss nachweisen kand#246;nnen, gute Englischkenntnisse, Erfahrungen im Vertrieb innerhalb der Industrie sowie Erfahrung im Pharma-Marketing haben. Idealerweise haben Sie Kenntnisse der Mand#228;rkte USA, England und Zentraleuropa.Sie sind in der Lage nach einer kurzen Einfand#252;hrungsphase selbstand#228;ndig zu arbeiten und sind offen fand#252;r den Aufbau von Beziehungen zu Vertriebspartnern im Ausland.Sind Sie Vetriebler mit einer Affinitand#228;t fand#252;r kreatives und selbstand#228;ndiges Arbeiten? Dann melden Sie sich bei uns.Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacien Délégué  Responsable AQ]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob48741035ABBEF91F482579F5001FC42B</referencenumber>
<City><![CDATA[Centre]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacien-D-and-amp-SHARP233l-and-amp-SHARP233gu-and-amp-SHARP233-Responsable-AQ_1641124.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Rejoignez un laboratoire de dimension internationale en tant que Responsable AQ and#38; Pharmacien Dand#233;land#233;guand#233; de son site de Distribution. Vos missions: Vous serez notamment le garant du systand#232;me AQ local et de son application. Vous serez aussi land#146;interlocuteur des fabricants et sous-traitants au niveau de la qualitand#233; (audits et inspections). Vous serez and#233;galement chargand#233; de la liband#233;ration des lots de produits finis et de leur traand#231;abilitand#233;.Vous serez accompagnand#233;(e) de deux techniciens qualitand#233; (management direct) et reporterez au PRI and#38; Responsable AQ basand#233; au siand#232;ge. Votre profil:-Pharmacien thand#233;sand#233;(e) et inscriptible en section B en tant que Pharmacien Dand#233;land#233;guand#233; ;-Expand#233;rience de 4 ans minimum ;-Maand#238;trise des BPF;-Anglais courant ;-Dand#233;marrage ASAP ;Vous devez obligatoirement and#234;tre inscriptible en section B en tant que Pharmacien Dand#233;land#233;guand#233;Envoyez-moi vite votre CV sous format Word.Je suis Benjamin MAURICE de Real Pharma, cabinet de recrutement spand#233;cialisand#233; dans lindustrie pharmaceutique. Je travaille avec de nombreux clients CRO, laboratoires pharmaceutiques ou biotechs, ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Medical Device  Illinois  Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2334CF9BDA5A236D482579F5001FC43B</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Medical-Device-Illinois-Contract_1641125.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading Medical Device company is seeking a skilled professional to fill the role of Quality Engineer.  The company, located in Illinois, specializes in the development and manufacturing of non invasive medical devices.  As a global leader, the company is focused on providing the best quality products to ensure excellent service and exceed patient expectations.  With U.S. sales growing year over year the company seeks to expand its market share by continually developing new technologies.The Quality Engineer is responsible for ensuring products are compliant.  This position is responsible for managing a team of engineers, conducting internal audits, and administering product tests.  The Quality Engineer will present findings to the Senior Management team.  All compliance and quality issues relating to the product will be addressed by this position.The candidate must have the following qualifications:- B.S. in Mechanical/Electrical Engineering or related field- 5+ years experience in medical device field- Familiar with FDA rules and regulation- Strong managerial skills- Strong communication skillsIf you are interested in this position apply now or contact Dana Leone at 312-453-9088 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director of Corporate Quality Audits]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob712478D4D8C46ADA482579F5001FC448</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Associate-Director-of-Corporate-Quality-Audits_1641127.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A multinational Pharmaceutical company with a Global presence is currently recruiting for a Senior Quality Assurance and Compliance Manager. Based in the South East you will be responsible for all activities including audit and inspection readiness, supplier certification and compliance management within global function.  As the Senior Quality Assurance Manager: -You will be responsible for Audit and Inspection Readiness-Assure integrated audit program is implemented including risk assessments, scheduling, execution and reports.-Develop internal auditor training program for EU. -Inspection readiness activities including training colleagues across regulatory interactions.-In conjunction with other colleagues you will participate in continuous improvement efforts.-Maintains awareness of current pharmaceutical compliance trends. Based on overall business need, the job function may also include: Supplier Certification-You will be the QA point of contact for Supplier Management -Collaborate with Quality Operation and develop clear roles and responsibilities for supplier certification qualification.-Interface with Global Quality Assurance to align supplier certification requirements If you are interested you must:-Relevant cGMP experience (through holding a QA position or a manufacturing or related position).-In depth knowledge of cGMP and the principles and concepts of relevant quality processes and quality systems based on previous roles-Detailed understanding of the cGMPs, quality systems and drug process-Detailed, demonstrable knowledge of GMP regulations and the Orange guide.This is an excellent position focussed around Compliance and Quality Management with a global scope and autonomy. You will liaising with senior stakeholders able to make a difference to the global function. If you are interested please send an updated CV to John Morkus or call 0207 758 7311 for further details.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Manager gesucht!  Medizintechnik]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFE2AB0AA965863C2482579F5001FC455</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Quality-Manager-gesucht-Medizintechnik_1641128.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein weltweit bekanntes Unternehmen im Bereich der Medizintechnikund hat seinen Standort in der Nand#228;he von Mand#252;nchen. Weiterhin zeichnet sich das Unternehmen auch mit seinen individuellen Weiterentwicklungsmand#246;glichkeiten und Fand#246;rderprogrammen fand#252;r Mitarbeiter aus.  Zum nand#228;chstmand#246;glichen Zeitpunkt suche ich einen Senior Manager fand#252;r das Qualitand#228;tsmanagement Team.Aufgaben:- Lieferantenaudits- Prozessoptimierung- Risikoanalysen- Enge Zusammenarbeit mit der Entwicklung- Stellvertretung der QM LeitungAnforderungen:Gesucht wird ein neuer Mitarbeitet mit langjand#228;hriger Medizintechnik Erfahrung..Sie sollten bereits mehrere Jahre in der Qualitand#228;tsabteilung gearbeitet haben und bevorzugt Kenntnisse oder Erfahrung aus der Entwicklung mitbringen.  Der Umgang mit Risikoanalysen ist fand#252;r Sie geland#228;ufig und Sie  bringen ein hohes Qualitand#228;tsbewusstsein mit. Ihr Ansprechpartner ist Simone LeberTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, and#252;ber den Online Bewerbungslink oder an and#60;band#62; s.leber(at)realstaffing.com and#60;/band#62; und rufen Sie mich an. Weiterhin besetze ich weitere spannende Positionen im Bereich Qualitand#228;t in der Medizintechnik. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete  Ihnen neue Perspektiven.  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[<b> Qualitätsingenieur im Raum Stuttgart <b>]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9427BA08071D507A482579F5001FC461</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/-and-amp-SHARP60b-and-amp-SHARP62-Qualit-and-amp-SHARP228tsingenieur-im-Raum-Stuttgart-and-amp-SHARP60-b-and-amp-SHARP62_1641129.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Pharma berand#228;t an mehreren Standorten weltweit Unternehmen bei der Besetzung von Positionen in den Geschand#228;ftsfeldern Pharma und in der Medizintechnik. Sie kand#246;nnen von diesem Knowhow profitieren, denn:Ab sofort suche ich fand#252;r ein and#60;band#62; Medical Devices Unternehmenand#60;/band#62; Sie alsand#60;band#62; Qualitand#228;tsingenieur im Raum Stuttgart and#60;/band#62;and#60;band#62; Erkennen Sie sich wieder? and#60;/band#62;and#60;liand#62; Technisches oder naturwissenschaftliches Studium oder vergleichbare Ausbildungand#60;/liand#62;and#60;liand#62; Kenntnisse der Standards ISO 13485, ISO 14971, FDA  and#60;/liand#62;and#60;liand#62; Berufserfahrung in der Medizintechnikand#60;/liand#62;and#60;band#62; Ja? Dann senden Sie mir noch heute Ihren Lebenslauf an s.leber(at)realstaffing.com! and#60;/band#62;and#60;band#62; Das sind Ihre Aufgaben: and#60;/band#62;and#60;liand#62; Bearbeitung von Reklamationen and#60;/liand#62;and#60;liand#62; Validierungand#60;/liand#62;and#60;liand#62; Unterstand#252;tzung bei Prozessoptimierungenand#60;/liand#62;and#60;liand#62; Durchfand#252;hrung von Auditsand#60;/liand#62;and#60;band#62; Sie mand#246;chten diskret nand#228;here Details erfahren oder sind sich bei dem ein oder anderen Punkt nicht sicher? and#60;band#62; Ihr Ansprechpartner ist Simone Leberand#60;/band#62;Tel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, max. 1MB, and#252;ber den Online Bewerbungslink oder an and#60;band#62; s.leber(at)realstaffing.com and#60;/band#62;und rufen Sie mich an. Besuchen Sie mein X I N G Profil fand#252;r weitere Informationen.and#60;band#62; https://www.xing.com/profile/Simone_Leberand#60;/band#62; and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Chef de projet affaires réglementaires DMOS]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5AF35CDBE5722840482579F5001FC46D</referencenumber>
<City><![CDATA[Paris]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Chef-de-projet-affaires-r-and-amp-SHARP233glementaires-DMOS_1641131.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Pourquoi rejoindre ce Laboratoire en tant que and#171; Chef de projet affaires rand#233;glementaires DMOS and#187;?-  Laboratoire pharmaceutique de renommand#233;e internationale dont le siand#232;ge europand#233;en est situand#233; en rand#233;gion parisienne.- Leader dans la dand#233;couverte de nouveaux traitements et de nouvelles technologies pour lamand#233;lioration de la vie des patients. -  Prand#233;sent and#224; linternational avec plus de 80 000 collaborateurs dans le monde.- Vous travaillerez dans un environnement dynamique et ouvert, vous permettant dand#146;acquand#233;rir une expand#233;rience professionnelle solide. Rattachand#233; au Responsable Affaires rand#233;glementaires, vous aurez pour mission :- De mettre en place les dispositions liand#233;es and#224; la loi DMOS au sein du dand#233;partement - De dand#233;clarer auprand#232;s du Conseil National de land#146;Ordre de toutes notifications conformand#233;ment and#224; la procand#233;dure en vigueur- De dand#233;clarer et contrand#244;ler les demandes de dons aux associations- Mettre and#224; jour et archiver des contrats DMOS ainsi que de la documentation juridique- Dand#146;and#234;tre land#146;interface auprand#232;s des diffand#233;rents services dans le suivi des dossiersVotre Profil :- De formation scientifique- Vous possand#233;dez une expand#233;rience de minimum 2 ans acquise dans un service affaires rand#233;glementaires.- Un bon niveau dand#146;anglais est indispensable and#224; land#146;oral comme and#224; land#146;and#233;crit. - Esprit de synthand#232;se et dand#146;analyse. Rigueur, organisation et esprit dand#146;and#233;quipe.Envoyez-moi vite votre CV sous format Word. La sand#233;lection des profils se fera dans un premier temps sur les cv envoyand#233;s.Je suis Jennifer Cohendy de Real Pharma, cabinet de recrutement spand#233;cialisand#233; dans lindustrie pharmaceutique. Je travaille avec de nombreux laboratoires pharmaceutiques, dispositifs mand#233;dicaux ou biotechs, ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Project Manager  Freelance  6 Months  1.0 FTE Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3EA8D549F32FC2AD482579F5001FC47B</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Project-Manager-Freelance-6-Months-10-FTE-Hessen_1641132.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading pharmaceutical company are currently seeking a  Freelance Clinical Project Manager to work on both National and International clinical trials at their office in the south of Germany. This is a global pharmaceutical company with a Global presence and a track record of making a real difference to individualsand#146; lives for over 100 years. Skills in the Management on Investigator Sites are required as below:and#149;Proactively manage a greater investigator site workload commensurate with experience, so that studies are run efficiently, and key study objectives are metand#149;Diabetes, Oncology or ZNS indications experience in the Clinical Research areaand#149;Ensure studies are run in Line with ICH/ GCP, local laws and the clients SOPs and proceduresand#149;Ensure patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirementsand#149;Inform the PI and site staff of all issuesand#149;Agree and develop corrective and preventive actions with PI and site personnel to close all open issuesand#149;Responsible for all aspects of site management from collaboration on site selection to study closeoutand#149;Train site staff on the protocol, protocol amendments and the clients processesand#149;Understand the product, the protocol and the therapy area in sufficient detail to be able to have appropriate discussions with the investigator team It is very essential for candidates to have come from a CRA / Monitoring background in order to understand the complications faced when conducting clinical trials and understand how to avoid and / or surmount them. As an International Pharmaceutical company there will be big involvement in International clinical trials and co-operation between colleagues and third parties in other countries.You will be working collaboratively with members of the Clinical Trial team to develop protocols, summaries, informed consent forms, patient information and other trial documents and provision of study specific training both internally and externally participating in the production of clinical trial documentation. Experience:and#149;CRA monitoring backgroundand#149;Diabetes experienceand#149;Long years of clinical studies experienceand#149;Report Reviewsand#149;Perform general administrative duties as neededand#149;Supervising of monitoringand#149;Fluent English and Germanand#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilityDURATION: 6 MONTHS + (Extension for another 6 months possible) LOCATION: Hessen RATE: and#128;80 - 100 PER  hour based on experienceIf you are interested in this position or would like more information please do not hesitate to contact Parminder Singh at Real Pharma on + 49 (0) 69 264 898 400and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance Associate  £25,000  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8DECAD26DEE09418482579F5001FC48A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Associate-and-amp-SHARP16325000-South-East_1641133.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a reputable consultancy with a pharmacovigilance focus.Only candidates with EU Pharmacovigilance experience can be considered.With ever-expanding operations, I am looking for a case processor with 1-2 years experience with an Oracle database. This position will be based in Guildford with a large team. This role will offer industry leading and award winning training and the opportunity to learn a wide remit of pharmacovigilance processes.Primary objective will be data entry work but a strong aptitude will be needed to take on varying work from numerous clients. Initiative and a pro-active nature are very important.If you feel you suit the above criteria, please get in touch ASAP.Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance Associate  £25,000  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob593A7B47B6E82491482579F5001FC496</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Associate-and-amp-SHARP16325000-South-East_1641134.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a reputable consultancy with a pharmacovigilance focus.Only candidates with EU Pharmacovigilance experience can be considered.With ever-expanding operations, I am looking for a case processor with 1-2 years experience with an Oracle database. This position will be based in Guildford with a large team. This role will offer industry leading and award winning training and the opportunity to learn a wide remit of pharmacovigilance processes.Primary objective will be data entry work but a strong aptitude will be needed to take on varying work from numerous clients. Initiative and a pro-active nature are very important.If you feel you suit the above criteria, please get in touch ASAP.Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Entwicklungsingeniuer für Operationsleuchtensysteme]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7FC9A085E709F343482579F5001FC4A6</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Entwicklungsingeniuer-f-and-amp-SHARP252r-Operationsleuchtensysteme_1641135.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde aus Hamburg sucht aktuell einen mechanischen Entwicklungsingenieur fand#252;r die Konstruktion von Endoprothesen.Ihre Tand#228;tigkeiten:- Design, Entwicklung und Konstruktion von Endoprothesen- Modellierung mit CAD Zeichnungen- Dokumentation, Validierung, und Qualitand#228;tssicherung von Gerand#228;ten  - Das Erstellen von Protokollen fand#252;r die Zulassung von Produkten Fand#252;r diesen Job brauchen Sie ein abgeschlossenes Studium in Maschinenbau, Feinwerktechnik oder Medizintechnik. Idealerweise bringen Sie 2 Jahre Berufserfahrung in der Konstruktion und Entwicklung mit. Sehr gute CAD SolidWorks und Englisch Kenntnisse sollten vorhanden sein. Erfahrung in der Entwicklung von Endoprothesen ist von Vorteil. Habe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Josand#233; Ramand#237;rez Bucheli (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Manager  Hematology  Pharma!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA1E5464688D3FD75482579F5001FC4B5</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Manager-Hematology-and-amp-SHARP150-Pharma_1641136.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mand#246;chten Sie in einem Unternehmen beschand#228;ftigt sein, indem der Fokus auf der Behandlung von seltenen Krankheiten liegt? Mand#246;chten Sie auch mit Ihrer Leistung signifikant Ihren Anteil zum Firmenerfolg und zur Gesundheit der Patienten beitragen?Mand#246;chten Sie international arbeiten und sind bereit, Reisen ins Ausland in Kauf zu nehmen?Dann sollte diese Stelle fand#252;r Sie als Product Manager im Bereich Hematology sehr interessant sein. Idealerweise erfand#252;llen Sie als interessierter Kandidat folgende Kriterien:and#149; abgeschlossenes Studium der BWL oder der Naturwissenschaftenand#149; sehr gute Marketing-Kenntnisse, vor allem im strategischen Marketingand#149; Erfahrung innerhalb der Pharmaindustrieand#149; idealerweise haben Sie Ihre Industriekenntnisse im Bereich der Hematology   gesammeltand#149; verhandlungssicheres Englischand#149; ReisebereitschaftBewerben Sie sich noch heute und nutzen die Chance auf eine interessante Position mit internationaler Ausrichtung.Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Wir freuen uns auf Sie.Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SeniorClinical Research Associate home based]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob55AEA40E1CDA8E66482579F5001FC4C1</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Clinical-Research-Associate-home-based_1641138.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is is a global CRO providing the full range of Phase I to IV clinical development services and has broad therapeutic expertise. Furthermore the company offers fast career progression, international opportunities and good payment.Currently I am looking for experienced CRA (clinical research associate) with a very good knowledge in oncology. Here are some more details about your profile:+ university degree in a science related field or certified health care professional or equivalent experience+ in depth knowledge of ICH-GCP, EU and FDA requirements+ excellent German and English language skills (spoken and written)+ willingness and#38; ability to travel (approx. 40%)Looking forward to your application and for further questions please feel free to contact me. E-mail: y.kamenova (at) realstaffing.com,  phone: +49 69 264 898 400Best regards,Yuliyana Kamenova and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Study Nurse  Hessen  1.0 FTE (4 x Onsite)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob309B1082652B4214482579F5001FC4CD</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Study-Nurse-and-amp-SHARP150-Hessen-10-FTE-4-x-Onsite_1641139.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Freelance Study Nurse and#150; Hessen / 1.0 FTE (4 x Onsite)My client is an international specialty Pharma Company in the heart of Hessen with a truly great environment to work in. They are currently seeking a Freelance Study Nurse for 6 months+. The role offers a great opportunity for those who may be looking for a new challenge in life. You should also have a very strong interpersonal skills and good experience in the Clinical Research area. Also excellent organizational and time management skills are required. Key Responsibilities:and#149;Helping and supporting the  Clinical Research Associates Teamand#149;Long years of clinical studies experienceand#149;Report Reviewsand#149;Assisting Clinical Trialsand#149;Is responsible for writing Agenda and#38; Minutes and#149;Provide practical support to the Clinical Operations group in the set up of the administration for the management of Clinical Trials and#149;Filing/archiving of documents in-house in line with GRT SOPand#146;s in close operation with the Clinical Trial Documentation and Archiving Unit  Expertise and Complexity:and#149;Clinical experience preferredand#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilitySalary/ Duration:and#149;Negotiableand#149;Start 01.06.2012and#149;End  01.12.2012 (with option on extension)The recruitment process will be a 1 Stage Face to Face interview with the Project Manager Onsite to meet the candidate in person.The client is located in Hessen which has excellent domestic and international access including the Frankfurt Airport and a very good rail connection. As a specialist recruiter in Clinical Research positions for Pharmaceutical clients in Germany and Switzerland, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.Apply now! Call Parminder Singh at +49 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head Quality  Biorpharmaceuticals  Tirol (mw)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF6CA8BEBCD896E4E482579F5001FC4D9</referencenumber>
<City><![CDATA[Tirol]]></City>
<Country><![CDATA[AUSTRIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Head-Quality-and-amp-SHARP150-Biorpharmaceuticals-and-amp-SHARP150-Tirol-m-w_1641140.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist einer der weltweit fand#252;hrenden Entwickler und Hersteller von patentfreien pharmazeutischen und biotechnologischen Arzneimitteln und Wirkstoffen und and#60;band#62; sucht Sie and#60;/band#62; als Leiter/ in eines Teilbereichs der Quality Unit.Es erwartet Sie ein aufgeschlossenes und motiviertes Team und vielfand#228;ltige Aufgaben. Das Unternehmen wand#228;chst seit Jahren kontinuierlich und bietet Ihnen langfristig sehr gute Perspektiven, auch an anderen Standorten.Sie sollten einen naturwissenschaftlichen Hintergrund und profunde Erfahrung im GMP-regulierten pharmazeutischen Umfeld mitbringen. Erfahrung im Bereich der (Steril-) Herstellung und/ oder Qualitand#228;tssicherung und/ oder Qualitand#228;tskontrolle, sowie erste Erfahrung in Mitarbeiterfand#252;hrung qualifizieren Sie weiterhin.Sie sollten Lust haben sich persand#246;nlich und fachlich einzubringen und Ihre, sowie die Visionen des Unternehmens in Teamarbeit umzusetzen und voranzutreiben.Klingt das interessant fand#252;r Sie? and#60;band#62;  Ich freue mich auf Ihre Bewerbungsunterlagen und gebe Ihnen gerne mehr Informationen zu dieser und anderen Positionen. and#60;/band#62; Melden Sie sich gerne bei mir, auch wenn diese Position nicht genau dem entsprechen sollte, was Sie sich vorstellen. Ich bin spezialisiert auf den Bereich Quality Management. Dort betreue ich unsere Kunden aus der pharmazeutischen und biotechnologischen Industrie und betreue ein umfangreiches Portfolio an Festanstellungen und habe sicherlich auch die passende Stelle fand#252;r Sie.and#60;band#62; Barbara Reist, Real Staffing Group  and#60;/band#62;and#60;band#62; Quality Management and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: b.reist (at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Spezialist für das Rh.MGebiet Kosmetunt.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7F54491DE260C26D482579F5001FC4E7</referencenumber>
<City><![CDATA[Rheinland]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Spezialist-f-and-amp-SHARP252r-das-Rh-M-Gebiet-Kosmetunt_1641141.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein weltweit agierendes und forschendes Kosmetikunternehmen im Rhein Main Gebiet, das in der Entwicklung von Kosmetikprodukten tand#228;tig ist. Im Moment wird dort ein Quality Assurance Spezialist gesucht.Ihre Tand#228;tigkeiten:Als Quality Assurance Spezialist gestalten Sie angemessene Vorgaben der GMP hinsichtlich Qualitand#228;t, Praktikabilitand#228;t und Wirtschaftlichkeit. Das Erstellen der SOPs, Audits und weitere Aufgaben der Qualitand#228;tssicherung. Ihr Profil:- Abgeschlossenes Studium der Pharmazie, Biotechnologie, Chemie oder in einem and#228;hnlichen Bereich- Mehrere Jahre Erfahrung als Qualitand#228;tssicherheitsbeauftragter in der Pharmaindustrie oder Kosmetikindustrie- Sehr gute MS Office und Lotus Kenntnisse- Fachwissen and#252;ber GMP- Flieand#223;ende Deutsch-, Englischkenntnisse und Italienischkenntnisse vom Vorteil- Bis zu 30 % Reisetand#228;tigkeit- Starke analytische und kommunikative Fand#228;higkeiten- Zielstrebig und teamorientiertHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen unter s.chaudhry(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Quality Unit  m f  BadenWuerttemberg]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE5AE8E801233B610482579F5001FC4F3</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Head-of-Quality-Unit-and-amp-SHARP150-m-f-and-amp-SHARP150-Baden-Wuerttemberg_1641142.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is an international service provider for the pharmaceutical industry and looking for a Head of Quality Unit for pharmaceutical packaging.There is a team of 8 securing the quality compliance on site including Quality Assurance, Quality Control and the Quality Management System.Your tasks:* Develop/ maintain/ apply quality requirement and standards (in an environment that values GMP, CI, 5S, Six Simga, lean manufacturing etc.)* Directing quality activities on site, including - Managing quality of materials and finished products - Documentation, Change, Deviation, CAPA, Complaint management - Coordination of internal and external audits* Establishing/ maintaining site quality manual and procedures* Communicating quality requirements to employees* Participation in optimization of processes, procedures, products* Site representative to global quality team Your profile:* Degree in pharmacy, engineering, chemistry or a similar scientific field* Significatnt experience in either pharmaceutical/ medical devices/ packaging component maufactuer* Profound knowledge of applying regulations (e.g. GMP and current industry practice)* Thorough knowledge of quality control and quality assurance operations* Knowledge of ISO 15378/ 9001 and Continuous Improvement Tools* Good knowledge of current pharmaceutical industry needs and expectations* Good German and English communication skills* leadership experience would be preferable* You should be willing to travel to worldwide sites, conferences and customers from time to timeIf you are interested in this role I am looking forward to receiving your current CV (please as Word document) and to make an appointment for a first phone call to get to know each other!and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pre Clinical Project Manager Freelance 1.0 FTE south Germany]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBF2081FB07DF784E482579F5001FC4FF</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pre-Clinical-Project-Manager-Freelance-10-FTE-south-Germany_1641143.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Pre-  Clinical Project Manager / Freelance / 6 Months / 1.0 FTE/ South GermanyA leading pharmaceutical company are currently seeking a  Freelance Pre- Clinical Project Manager to work on both National and International clinical trials at their office in the south of Germany. This is a global pharmaceutical company with a Global presence and a track record of making a real difference to individualsand#146; lives for over 100 years. Skills in the Management on Investigator Sites are required as below:and#149;Proactively manage a greater investigator site workload commensurate with experience, so that studies are run efficiently, and key study objectives are metand#149;Have a very good understanding of Research and Development of new substances in Project management of Pre Clinical studiesand#149;Ensure studies are run in Line with ICH/ GCP, local laws and the clients SOPs and proceduresand#149;Ensure patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirementsand#149;Inform the PI and site staff of all issuesand#149;Agree and develop corrective and preventive actions with PI and site personnel to close all open issuesand#149;Responsible for all aspects of site management from collaboration on site selection to study closeoutand#149;Train site staff on the protocol, protocol amendments and the clients processes It is very essential for candidates to have come from a CRA / Monitoring background in order to understand the complications faced when conducting clinical trials and understand how to avoid and / or surmount them. As an International Pharmaceutical company there will be big involvement in International clinical trials and co-operation between colleagues and third parties in other countries.You will be working collaboratively with members of the Clinical Trial team to develop protocols, summaries, informed consent forms, patient information and other trial documents and provision of study specific training both internally and externally participating in the production of clinical trial documentation. Experience:and#149;CRA monitoring backgroundand#149;Oncology experienceand#149;Long years of clinical studies experienceand#149;Report Reviewsand#149;Perform general administrative duties as neededand#149;Supervising of monitoringand#149;Fluent English and Germanand#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilityDURATION: 6 MONTHS + (Extension for another 6 months possible) LOCATION: South Germany RATE: and#128;80 - 100 PER  hour based on experienceIf you are interested in this position or would like more information please do not hesitate to contact Parminder Singh at Real Pharma on + 49 (0) 69 264 898 400and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualified Person voor loonverpakker]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4D387DD01903DC90482579F5001FC514</referencenumber>
<City><![CDATA[Zuid]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualified-Person-voor-loonverpakker_1641144.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een contract manufacturer in het zuiden van het land is op zoek naar een Qualified Person ter versterking van hun team.Deze organisatie is ooit begonnen als een echt familie bedrijf maar inmiddels zijn ze uitgegroeid tot een grote speler in de Nederlandse markt. Op dit moment werken er 130 mensen, verspreid over 2 sites waar al meer dan 600 verschillende geneesmiddelen geproduceerd worden, zowel solide als steriele toedieningsvormen. Op dit moment zijn er twee QPand#146;ers en een hoofd QP werkzaam die deze producten vrijgeven. Echter, wegens de continue groei van het aantal aanvragen vanuit de markt zijn zij op korte termijn zoek naar een Qualified Person. In de functie van Qualified Person ben je samen met de andere QPers verantwoordelijk voor het gehele vrijgifteproces. Daarnaast houd je je bezig met het monitoren van het kwaliteitssysteem (GMP), Change Control en treed je bij afwijkingen in overleg met productie. Op middellange termijn zal je je meer en meer gaan focussen op audits (intern en extern).  Secundaire voorwaarden:- Op basis van je ervaring een jaarsalaris van maximaal and#128;80000- 25 vakantiedagen + 13 atv dagen en overige interessante secundaire voorwaardenFunctie eisen:- MSc farmacie- Kennis van magistrale bereidingen- Werkervaring in een GMP omgeving- Nederlands: vloeiend in woord en geschriftBen je geand#239;nteresseerd en wil je meer weten over deze functie, druk dan op de and#145;applyand#146; button en upload je cv ter attentie van Gwen Reniers.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Manager, Pharma, greater area Chur]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE64F5A6CFF49F2BB482579F5001FC520</referencenumber>
<City><![CDATA[Switzerland]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Manager-Pharma-greater-area-Chur_1641145.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients of the pharmaceutical industry is currently looking to fill the position of a Product Manager.    Product Manager, Pharma, greater area ChurThe company is looking for:-Background in pharmaceutical or from the cosmetics industry -Knowledge/experience of marketing in the pharmaceutical industry is a plus-Outstanding communication skills -Fluency in English and German (written and oral)The role:-Classical marketing activities e.g. implementation of product strategies-Market analyses e.g. competitors  -Being scientific and having the skills to translate this into marketingThe company:-Location: greater Chur area offering traditional Swiss flair-Established of more than 50 years in CH -Values stand for offering exceptional service while being innovativeYou gain a negotiable salary package as well as career opportunities!I am Corinna Kutzner, a recruitment specialist in marketing recruitment sector. I am currently working with many organisations in this area only in Switzerland. This means that I can offer you multiple vacancies for your job search. For more information on this, or any other similar roles, please apply online or contact Corinna Kutzner on +41 (0) 43 50 80 972.Key words: Marketing, Pharmaceutical, Product Manager, Junior, Switzerland, Marketing Strategies, Chur, Marketing Tools, Implementation, Cosmetics, English, German, Products]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QC Team Leader  6 months  Walloon Brabant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob064EA6FDD15F122B482579F5001FC52C</referencenumber>
<City><![CDATA[Walloon Brabant]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/QC-Team-Leader-6-months-Walloon-Brabant_1641146.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[QC Team Leader and#150; 6 months and#150; BrusselsMy client is looking for a QC Team Leader for a 6 months contract in Walloon Brabant. You will need to manage the execution of a range of both well-defined and adhoc testing activities through a a team of lab technicians in order to ensure testing results delivery in line with qualitative and quantitative targets. Project: and#149;Oversee the detailed laboratory activities of one shift (+/- 7 techniciansand#149;Stability tests, raw material, semi-finished products, finished products, in process controls, cleaning verification, and#133; and#149;Set priorities and must be able to readjust planning in case of unforeseen events. and#149;You will be in internal discussion with the production, project managers abd Rand#38;D, QA and Supplyand#149;External discussion with suppliers/service providers and regular contact with customers. and#149;People management, organization, troubleshooting and reportingand#149;Verify and control test result reports prepared by the laboratory technicians in order to decide about the release and sign offand#149;Technology transfer and method validationand#149;QC methods and procedures Profile: -Master in science or equivalent by experience-Approximately 5 year experience in a lab environment of which by preference 2 year experience in people management-Able to understand all processes in and outside the companyDuration:-Duration: 6 months-Location: Walloon Brabant-Start date: Negotiable-Rate: Market rate We will endeavour to respond to your application ASAP. However, there may be times when it is not possible to reply to all applications, due to high volumes of enquiries. This is sometimes the case for unsuccessful applications to one of our vacancies. We apologise for this and can reassure you that we will keep your details and contact you in the future should any suitable positions arise.If interested, do not hesitate to contact Olivier Buysschaert on 02/610.59.59and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Key Account Manager in der Pharmazie (bei Lohnhersteller) gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob09E8C10F63940213482579F5001FC537</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Key-Account-Manager-in-der-Pharmazie-bei-Lohnhersteller-gesucht_1641147.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein in Nordrhein-Westfalen ansand#228;ssiges Unternehmen sucht derzeit mehrere Key Accounter mit Erfahrung bei einem Lohnhersteller in der Pharmazie. Ihre Aufgaben:and#149;Aufbau eines Key-Account Gebietes mit allen relevanten Tand#228;tigkeitenand#149;aktive und zielgerichtete Kundenbetreuung and#149;Kontaktaufbau zu Meinungsbildnern and#149;Erstellung von individuellen Angeboten mit Ziel des Abschlusses eines Rahmenvertragesand#149;Entwicklung von Maand#223;nahmen zur Vermeidung von Umsatzrisikenand#149;Entwicklung von Strategien (Konzepten) zum Aufbau eines Netzwerkes zur Steigerung von Umsatz und Ertragand#149;Durchfand#252;hrung von Marktbeobachtungenand#149;Analyse von Kennzahlen und deren Umsatzentwicklungand#149;Organisation und Kontrolle von Aktionen bei Fachmessen und Kongressenand#149;Mitwirkung bei der Entwicklung neuer Versorgungskonzepteand#149;Erarbeitung von langfristigen Strategien zur Bindung von TopkundenIhr Profil:and#149;Ausbildung zum Pharmareferent (w/m) oder vergleichbare Ausbildung, Studium der Medizin, Biologie, BWL mand#246;glichand#149;mindestens 3 and#150; 5 Jahre Berufserfahrung bei einem Lohnhersteller in der Pharmazie. and#149;selbststand#228;ndige, kreative Arbeitsweise und Organisationsgeschickand#149;Erfahrung in der Durchfand#252;hrung von Messen und Workshopsand#149;naturwissenschaftliche Kenntnisse und Kenntnis des gesundheitspolitischen Umfeldesand#149;sehr gute MS-Office-Kenntnisseand#149;and#220;berzeugungsstand#228;rke und Verhandlungsgeschickand#149;Teamfand#228;higkeit und Kontaktfreudigkeitand#149;ReisebereitschaftBei Interesse melden Sie sich bitte unter:Lisa Schumacher I Recruitment ConsultantMarketing and#38; Sales Real Staffing GroupRecognising talentl.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[<b> Core Data Sheet Expert Drug Safety (mw)<b>]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9617BD563B75B38B482579F5001FC544</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/-and-amp-SHARP60b-and-amp-SHARP62-Core-Data-Sheet-Expert-Drug-Safety-m-w-and-amp-SHARP60-b-and-amp-SHARP62_1641148.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62; Core Data Sheet Expert Drug Safety (m/w)and#60;/band#62;Ab sofort suche ich im Namen eines forschenden Pharmaunternehmens einenand#60;band#62; Core Data Sheet Expert Drug Safety (m/w) and#60;/band#62;Hier erwarten Sie u.a. folgende and#60;band#62; Aufgabenand#60;/band#62;:Sie werden als medizinischer Ansprechpartner in der Pharmakovigilanz fand#252;r die Betreuung und Bearbeitung der Company Core Data Sheets zustand#228;ndig sein. Sie arbeiten an den wissenschaftlichen Verpackungstexten und kand#252;mmern sich um das update der Core Data Sheets indem Sie auf Ihren wissenschaftlichen Hintergrund zurand#252;ckgreifen.  Fand#252;r diese Stelle bringen Sie folgende and#60;band#62; Eigenschaftenand#60;/band#62; mit:and#60;liand#62;  abgeschlossenes Studium der Pharmazie oder der Naturwissenschaftenand#60;liand#62;  Affinitand#228;t dazu und Erfahrung mit der Arbeit mit wissenschaftlichen Textenand#60;liand#62;  praktische Erfahrung in der Medizinisch Wissenschaftlichen Abteilungand#60;liand#62;  zuverland#228;ssige Arbeitsweiseand#60;liand#62;  Deutsch und Englisch flieand#223;end in Wort und Schriftand#60;band#62; Das trifft auf Ihre Person zu? Nur zu! Schicken Sie mir gerne Ihren aktuellen CV. and#60;/band#62;Sie werden hingegen vom internationalen Umfeld des Unternehmens profitieren. Nicht nur das Unternehmen an sich ist ein sehr guter Arbeitgeber, sondern auch die Mitarbeiter sind offen und die Teamatmosphand#228;re stimmt.Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Frau Hanna Holowaty wenden. and#60;band#62; Hanna Holowaty, Real Staffing Group  and#60;/band#62;and#60;band#62; Medical Affairs/ Pharmakovigilanz and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: h.holowaty(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SoftwareEntwicklungsingenieur Medizintechnik]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCA5B03F391A608B0482579F5001FC54F</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Entwicklungsingenieur-Medizintechnik_1641149.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Die Real Staffing Group ist eine spezialisierte Personalberatungsagentur fand#252;r die Pharma- und Medizintechnikindustrie. Wir vermitteln Fach- und Fand#252;hrungskrand#228;fte. Mein Kunde, der in Baden-Wand#252;rttemberg ansand#228;ssig ist, suche ich zur Erweiterung des Teams, einen Software-Entwicklungsingenieur Medizintechnik.Software-Entwicklungsingenieur MedizintechnikAufgaben:Als Software-Entwicklungsingenieur Medizintechnik sind Sie fand#252;r die Planungssoftware und Reporting verantwortlich. Somit liegen Ihre Aufgaben in der Entwicklung anwendugsorientierter Software. Sie fand#252;hren eigenstand#228;ndig Projekte durch. Sie sind fand#252;r die Erstellung von Spezifikationen zustand#228;ndig.Profil:Studium der Informatik, Elektrotechnik, Naturwissenschaft o. and#228;.Sie bringen mind. 2 Jahre Berufserfahrung in der Softwareentwicklung mit. Sehr fundierte Kenntnisse in C/C++ und C# sind dabei erforderlich. Sie haben bereits Kenntnisse in Anforderungen bzw. Requirementsmanagement sammeln kand#246;nnen. Sie sind bereits mit UML vertraut.Von Vorteil sind Kenntnisse in: QT, VTK, Bildentstehungstools 3D-Slicer etc.Sie wollten schon immer Programmierbare Medizinsysteme entwickeln? Sie wollen Ihre offene Persand#246;nlichkeit in einem internationalem einbringen?Dann bewerben Sie sich jetzt als Software-Entwicklungsingenieur MedizintechnikSenden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Manager (international tätig) für die Pharmaindustrie gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob53209A664172BEA6482579F5001FC55A</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Manager-international-t-and-amp-SHARP228tig-f-and-amp-SHARP252r-die-Pharmaindustrie-gesucht_1641150.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein Pharmaunternehmen im Umkreis Hamburg und sucht derzeit zum nand#228;chstmand#246;glichen Termin einen Product Manager. Das Unternehmen bietet nach einer gewissen Zeit die Mand#246;glichkeit zum Senior oder zum Abteilungsleiter aufzusteigen. Kinderbetreuung wand#228;re durch einen betrieblichen Kindergarten ebenfalls mand#246;glich. Ihre Aufgaben: Akquise von Neukunden und aktives Lieferantenmanagement inklusive der persand#246;nlichen Betreuung vor Ort Ausbau und Optimierung des Produktportfolios Markt und Wettbewerbsbeobachtung Unterstand#252;tzung bei der Markteinfand#252;hrung neuer ProdukteIhre Anforderungen: Sie verfand#252;gen and#252;ber eine abgeschlossene Ausbildung im Auand#223;enhandel oder ein Studium, Fachrichtung Marketing und Vertrieb und sind seit mehreren Jahren im internationalen Vertrieb tand#228;tig. Durch Ihre bisherige Tand#228;tigkeit in der pharmazeutischen Industrie besitzen Sie detaillierte Kenntnisse and#252;ber den deutschen und europand#228;ischen Markt.Wir setzen verhandlungssichere Englischkenntnisse voraus, Kenntnisse einer weiteren Fremdsprache sind von Vorteil. Wenn Sie offen, zuverland#228;ssig, belastbar und teamfand#228;hig sind, erwartet Sie eine interessante und abwechslungsreiche Aufgabe mit Raum fand#252;r Eigeninitiative und Verantwortung.Lisa Schumacher I Recruitment ConsultantMarketing and#38; Sales Real Staffing GroupRecognising talentTaunusanlage 18, 60325, FrankfurtTel:  +49 (0) 69 264 89 8400Fax: +49 (0) 69 264 89 8001www.realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Leiter Qualität mit hoher Personalverantwortung gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC6931B068CE876FE482579F5001FC567</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Leiter-Qualit-and-amp-SHARP228t-mit-hoher-Personalverantwortung-gesucht_1641151.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein innovatives Medizintechnik Unternehmen in Baden Wand#252;rttemberg suche ich eine gestandene Persand#246;nlichkeit. Das Unternehmen hat seine eigene Entwicklung and#38; Produktion vor Ort.Am Besten bringen Sie langjand#228;hrige Erfahrung in der Medizintechnik Branche mit und haben bereits ins der Funktion als Quality and#38; Regulatory Affairs Manager gearbeitet. Ihre Aufgabe besteht darin die Qualitand#228;tsabteilung zu leiten, sowie wird Reisebereitschaft erwartet. Kenntnisse der 21 CFR Part 820, 21 CFR Part 210 ,21 CFR Part 211, 21 CFR Part 11, ISO 13485 sind Ihnen geland#228;ufig. Durch Ihre Persand#246;nlichkeit kand#246;nnen Sie die Mitarbeiter fand#252;r sich gewinnen und auch Entscheidungen auf Management Ebene tragen. Die englische Sprache beherrschen Sie verhandlungssicher.Wenn fand#252;r Sie die oben aufgelisteten Punkte keine Fremdwand#246;rter sind und Sie sich als Leiter Quality behaupten mand#246;chten, dann kand#246;nnten Sie der richtige Mann oder die richtige Frau sein.Erwarten kand#246;nne Sie ein attraktives Gehalt in einem spannenden und schnell wachsenden Unternehmen.Gerne erhalten Sie diskret und fachlich kompetent weitere Details. Ihr Ansprechpartner ist Simone LeberTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, and#252;ber den Online Bewerbungslink oder an and#60;band#62; s.leber(at)realstaffing.com and#60;/band#62; und rufen Sie mich an. Weiterhin besetze ich weitere spannende Positionen im Bereich Qualitand#228;t in der Medizintechnik. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete  Ihnen neue Perspektiven. Besuchen Sie mein X I N G Profil fand#252;r weitere Informationen.https://www.xing.com/profile/Simone_Leber]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[(Senior) CRA officebased in Süddeutschland oder homebased]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7D7452B17CC24451482579F5001FC571</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-CRA-office-based-in-S-and-amp-SHARP252ddeutschland-oder-home-based_1641152.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist eine groand#223;e internationaltand#228;tige und sehr erfolgreiche CRO. Das Unternehmen sucht nach CRA oder Senior CRA office- oder home-based zu besetzen. Wenn Sie mind. 1 Jahr Monitoringerfahrung mitbringen, Interesse an interessanten Projekten und neuen Herausforderungen in einer erfolgreichen CRO haben, dann freue ich mich auf Ihre Bewerbung. Bitte senden Sie Ihren Lebenslauf als Word-Dokument. Bei weiteren Fragen helfe ich Ihnen unter folgenden Kontaktdaten diskret weiter:Yana ZinchukReal Staffing+49 (0)69 264 89 8400 y.zinchuk(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Project Manager für eine internationale CRO in Frankfurt]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB781C126F06DF2A3482579F5001FC57D</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Project-Manager-f-and-amp-SHARP252r-eine-internationale-CRO-in-Frankfurt_1641153.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r eine internationale mittelstand#228;ndige CRO mit dem Sitz in Frankfurt habe ich eineand#60;band#62;Clinical Project Managerand#60;/band#62;Stelle zu besetzen. Es handelt sich um eine office-based Stelle, Festeinstellung. Auand#223;er der Mand#246;glichkeit an interessanten Projekten mitzuarbeiten, bittet das Unternehmen eine gute Bezahlung und einen Firmenwagen dazu.Ihre Aufgaben:- Planung, Koordination und durchfand#252;hrung von klinischen Studien- Leitung des Studienteams- BudgetverantwortungIhre Qualifikation: - Mind. 1 Jahr Erfahrung als Clinical Project Manager- Frand#252;here Erfahrung als CRA wand#252;nschenswert- Erfahrung bei einer CRO vorausgesetzt- Verhandlungssicheres Englisch in Wort und SchriftIch freue mich auf Ihren Lebenslauf als Word-Dokument. Bei weiteren Fragen helfe ich Ihnen unter folgenden Kontaktdaten diskret weiter:Yana ZinchukReal Staffing+49 (0)69 264 89 8400 y.zinchuk(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Medical Writer für ein Pharmaunternehmen gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEA4B76C1B1A82843482579F5001FC587</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Medical-Writer-f-and-amp-SHARP252r-ein-Pharmaunternehmen-gesucht_1641154.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r meinen Kunden, ein groand#223;es internationales Pharmaunternehmen in Sand#252;ddeutschland, suche ich einen REGULATORY MEDICAL WRITER.Haben Sie: - Erfahrung in regulatory and#38; scientific writing?- Spaand#223; am Schreiben und Auswerten? - schon Publikationen verand#246;ffentlicht? - Naturwissenschaftliches Studium hinter sich?Es handelt sich um eine Festeinstellung, idealerweise office-based in Sand#252;ddeutschland.Ich freue mich auf Ihre Bewerbung. Bitte senden Sie Ihren Lebenslauf als Word-Dokument. Bei weiteren Fragen helfe ich Ihnen unter folgenden Kontaktdaten diskret weiter:Yana ZinchukReal Staffing+49 (0)69 264 89 8400 y.zinchuk(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Control Chemist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDC839DDBB853D42F482579F5001FC592</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Quality-Control-Chemist_1641155.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[We are currently seeking experienced quality control chemists for two contract roles based in  both Melbourne and Sydney.  and#60;band#62;The role will include the following:and#60;/band#62; and#149;QC and Stability Testing - wet chemistry and instrumental techniques.and#149;Calibration of various instruments within the laboratory. and#149;QC and Stability Testing of Bulk/Finished Products to.  and#60;band#62;To be successful candidates must have:  and#60;/band#62;and#149;A tertiary qualification in chemistry.and#149;At least 5 years experience in the pharmaceutical industry.and#149;have a sound knowledfe of the regulations governing the pharmaceutical industry (GLP, GMP, TGA etc.).and#149;Experience in HPLC analysis and trouble shooting.and#149;Experience with GC and/or AAS desirable.and#149;Good wet chemistry techniques.and#149;Sound written and communication skills.and#149;The ability to work shift workPlease send through your CV and note you will only be contacted if you are successful in making the shortlist.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Health Economist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA1B5B8A90AB5BDB2482579F5001FC59D</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Health-Economist_1641156.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, one of the worlds largest Pharmaceutical companies, is searching for a Health Economist for a part-time/flexible working arrangement long-term contract based in Sydney. Purpose:- To plan and#38; prepare high quality applications for reimbursement to the Pharmaceutical Benefits Advisory Committee (PBAC)- To plan and#38; prepare high quality applications, in collaboration with the Pricing Associate,  to the Pharmaceutical Benefits Pricing Authority (PBPA)- To collaborate with cross-functional colleagues to develop, communicate and execute risk sharing agreements with the Department of Health- To provide advice to internal customers on local reimbursement and#38; pricing strategies as required.- The role will have responsibility across PBAC submissions and have full end to end ownership, consequently dealing with all areas of the submissionRequirements:- Relevant qualifications or a tertiary degree in Pharmacy, Economics, Medicine or Health Sciences; - Experience in pharmaco-economics or health economics within the Australian, Canadian or UK pharmaceutical industry, or with a large evidence based related health care sector (Government or academia), or in consulting; - PBAC submissions experience- Excellent communication skills This role can offer a part time working option or flexible working arrangements if required. Apply now or for more information contact Gemma Macpherson on 02 8251 1100.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobEF155906DA3C7540482579F5001FC5A9</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Senior-Regulatory-Affairs-Associate_1641157.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you looking to move into a more senior role? Or just looking to move into a new and exciting company? Well this could be for you!The Company:Our client, a global Pharmaceutical company, is looking for a Senior Regulatory Affairs Associate. This established company is currently experiencing very strong growth over the last few quarters, due to its global success. The Role:I have an excellent role that I need to fill as soon as possible. If you fulfill the requirements of the job, please contact me today.Brief Job Description: -Tertiary education in Science (medical science, pharmacology or chemistry) -5-8 years RA experience working with prescription medicines is essential-experience working with medical devices is desired -project management skills -working knowledge of Australian and New Zealand regulatory requirements -able to advise and mentor associates -committed and passionate toward work -friendly and works well in a teamIf you have the drive and ambition to succeed combined with excellent communication skills and relevant industry experience then this could be the right opportunity for you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Medical Writer Maryland Phase 1]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC64114468DCBC40C482579F5001FC5B4</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Baltimore]]></State>
<url>http://www.engineerjob.us/job/Senior-Medical-Writer-Maryland-Phase-1_1641158.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of the largest CROs world-wide is seeking a friendly, team-oriented regulatory medical writing expert with management skills to work in an exciting, engaging and energetic company environment. Salary is highly attractive at up to and120k. This is a mainly on-site position based out of Maryland.As the senior medical writer in the phase 1 group, your main responsibilities include:-Preparing clinical documents such as clinical study reports and protocols for Phase 1 healthy volunteer studies-Collaborate with various groups in the team to facilitate client deliverables-Update clinical study and global regulatory submission document templates-Assist the Medical Monitor in the review, analysis and interpretation of data from clinical studies, including data files, tables, figures and listings -Oversee or assist in the planning and conduct of DSMB, Safety Review Committee, Cohort Review, Dose Escalation, Data Review or other study-related meetingsRequirements/Skills:-BS minimum-Work on-site in Maryland is a must-Excellent communication skills-PHASE ONE EXPERIENCE IS KEY! MUST HAVE Healthy Volunteer Study Experience!This company offers extremely competitive compensation and generous benefits package.  Donand#146;t miss this opportunity to join a growing and stable medical writing group at a company with lots of groundbreaking expansion!Send Resumes to Dandan Zhu at Real Pharma, contact me today at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager of Medical Writing  Associate Director level New Jersey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8469F36A1B1387AA482579F5001FC5BF</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Manager-of-Medical-Writing-Associate-Director-level-New-Jersey_1641159.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Exciting large global pharmaceutical company seeks Manager or Associate Director of Medical Writing in the Clinton, NJ area.  This company offers stable long-term job advancement opportunities as well as an encouraging team atmosphere.  The salary is highly competitive with the opportunity to hit 20% target bonus. This company has an impressive emerging presence and this inhouse medical writing team is definitely the place to be!Main responsibilities include:-Hands-on Writing of clinical documents under minimal supervision such as CSRs, IBs, narratives, NDAs, INDs, summaries of efficacy and safety, etc.-Adhering to regulatory and internal procedures and standards, templates and formats with consistency and independence-Working closely with various departments to ensure complete and smooth results-Work with fellow writers Requirements:-5+ years of solid medical writing experience-BS required, advanced degrees desired such MS or PhD-Highly capable team player with strong interpersonal skills-Leadership initiative, ability to multi-task and complete assignments on timeDo not miss this opportunity to get your dream medical writing job as a leader in regulatory medical writing in a stable, financially strong and international pharmaceutical company!  Apply today and send resumes to Dandan Zhu at Real Pharma; Reach me at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Remote  Medical Writer  Agency Experience Needed]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFC854BBDCC13BF44482579F5001FC5CB</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Remote-Medical-Writer-Agency-Experience-Needed_1641160.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Medical Writer required to join a New Jersey Medical Communications Group, to work on pharmaceutical/biotechnology promotional programs and initiatives.  Programs include advisory boards, speaker bureaus, and market research in such fields as neuroscience/psychiatry, gastroenterology, cardiology, endocrinology, and oncology.  You will play a direct role in content creation by writing and revising a range of materials.Additional responsibilities will include:-Interacting with physician faculty and client medical/marketing staffs to ensure that information is accurate, complete, on-message, and fully compliant - Managing submission and revision of materials through clientsand#146; medical-legal review process.- Travels to attend and report on program events and medical conferences- Attend program events (such as advisory boards) and prepare summary reportsYou should have:-3-5 years writing experience in Medical Communications Agency-Bachelorand#146;s degree or higher in English, communications, or a related field; or in the life sciences-Medical agency experience -Specific experience in any of the therapeutic areas above is a bonus This is a stable company, offering an exciting chance to take a role, and make a real, visible difference to the growth and direction of the business. Salary is commensurate upon experience and70-95K plus benefits. Please upload your resume today, and/or call Christian Williams at Real Pharma on 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Medical Writer Massachusetts]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34371C7577F499B0482579F5001FC5D7</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Principal-Medical-Writer-Massachusetts_1641161.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Exciting large global pharmaceutical company seeks principal medical writer in the Cambridge, MA area.  This company offers stable long-term job advancement opportunities as well as encouraging team atmosphere. Full Relocation will be provided - salary is also above market average at up to and140k for a principal writer with strong submission experience!Main responsibilities include:-Preparing clinical documents under minimal supervision such as CSRs, IBs, narratives, NDAs, INDs, summaries of efficacy and safety, etc.-Adhering to regulatory and internal procedures and standards, templates and formats with consistency and independence-Working closely with various departments to ensure complete and smooth results-Mentor and train junior writers or other peersRequirements:-Minimum of 4+ years of solid medical writing experience-BS required, advanced degrees desired-Highly capable team player with strong interpersonal skills-Leadership initiative, ability to multi-task and complete assignments on timeDo not miss this opportunity to get your dream medical writing job as a principal writer in a stable, financially strong and international pharmaceutical company!  Apply today and send resumes to Dandan Zhu at Real Pharma; Reach me at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Remote  Medical Director  New YorkNew Jersey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01E5279C7C92D045482579F5001FC5E2</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Remote-Medical-Director-New-York-New-Jersey_1641162.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Medical Communications Agency seeks a Medical Director to provide scientific strategy and execution of Med Comms programs.Key Responsibilities:-Leading the strategic development of program goals, concept development and proposal design/ writing. -Actively participating in new business pitches with existing and prospective clients-Delivering accurate information while complying and enforcing legal and regulatory requirements -Creating content for Manuscripts, Review Articles, Abstracts, Posters, Slide Decks, Advisory Board Material, etc. that is comprehensive and on strategy.-Responsible for scientific direction of client programs to ensure medical communication is accurate.-Managing customer expectations and customer delivery -Traveling to and manages on-site editorial needs. Qualifications/Requirements:- Advanced degree in the life sciences, pharmacology or medicine - 4-5 years+ experience in medical communications role within  medical communications industry. - Must have first-hand publications/scientific content development experience. - Project management experience with direct client contact regarding project delivery and content development needs This is a stable, global Company, offering an exciting chance to take a lead role, and make a visible difference to the growth and direction of the office. Salary is up to and150K plus benefits. Please upload your resume today, and/or call Christian Williams at Real Pharma on 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance  Drug Safety Associate  Hertfordshire  £28K]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34AF106FD6775CC4482579F5001FC5ED</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Drug-Safety-Associate-Hertfordshire-and-amp-SHARP16328K_1641163.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Leading global Pharmaceutical company urgently requires Pharmacovigilance Officer/ South East/ Hertfordshire area /London / South East and#163;23 - and#163;28K + bonus This role with suit someone with at least 6 months to 1 year experience in Pharmacovigilance with a focus to progress a long term career. Further training will be given. PV Operational Associate - Working closely with PV Project Managers - In charge of case submissions to MHRA, FDA, EMEA - Good understand of global regulations - Tracking all cases - Liaising with investigators - Good organisational and attention to detail is needed. This is an excellent opportunity to join a growing company that offers fast career progression. The role will grow with a opportunity to get training on PSUR and ASR report writing, SOP, and protocols. Apply now by sending a recent CV or call Leena Lalli on 02077587311 for more info.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Embedded Software Entwickler Raum München bis 65.000 EUR]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob56925FFB366968F3482579F5001FC5F8</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Embedded-Software-Entwickler-Raum-M-and-amp-SHARP252nchen-bis-65000-EUR_1641164.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Die Real Staffing Group ist eine spezialisierte Personalberatungsagentur fand#252;r die Pharma- und Medizintechnikindustrie. Mein Kunde, der in Raum Mand#252;nchen ansand#228;ssig ist, suche ich zur Erweiterung des Teams, einen Embeddes Software-Entwickler.Embedded Software-EntwicklerProfil:Studium der (technischen) Informatik, Elektrotechnik o.and#228;.Sie konnten bereits mehrjand#228;hrige Berufserfahrung in Embedded Software C/C++ sammeln. Sie haben ebenfalls sehr starke Kenntnisse in Debugger und Cross-Compilern. Fundierte Kenntnisse sind in der Echtzeitprogrammierung erforderlich.Medizintechnikerfahrung wand#228;re wunschenswert. Erfahrungswerte im Bereich Mikrocontroller und FPGA-Design sind vorteilhaft.Aufgaben:Sie sind fand#252;r die Embedded-Softwareentwicklung und Firmware verantwortlich. Sie entwickeln das Design und sind ebenso fand#252;r die Realisierung zustand#228;ndig. Dabei dokumentieren alle relevanten Schritte. Sie sind fand#252;r die Algorithmenentwicklung zustand#228;ndig und fand#252;r die objektorientierte Entwicklung. Sie wollen Ihre gewonnne Erfahrung unter Beweis stellen? Sie wollten schon immer mit sehr erfahrenden Embedded-Softwareentwicklern zusammen arbeiten?Dann bewerben Sie sich jetzt als Embedded Software - EntwicklerWeitere Angebote fand#252;r jederlei Erfahrungswerte sind vorhanden. Bitte kontaktieren Sie mich.Senden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract SAS Statistical Programmer  Germany  18 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5B57D074797D99BD482579F5001FC602</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-SAS-Statistical-Programmer-Germany-18-Months-_1641165.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a family owned, leading Pharmaceutical company in Germany with a major market presence both nationally and internationally due to their pioneering approach in the manufacture of leading Pharmaceutical products and their large investment policy into drug development.I have an excellent 18 month freelance / contract opportunity for a SAS Statistical Programmer to work for my client near Frankfurt due to the an explosive pipeline of new drug development that requires additional support from Statistical programmers.You will be providing SAS programming support to a number of clinical trials as part of a submission package to the FDA. Therefore you will be creating and validating analysis datasets, Tables, Figures and Listings.Experience:-5 +  years SAS Statistical Programming within the Pharmaceutical Industry SAS BASE / MACRO / STAT / GRAPH Creating and Validating Analysis Datasets, Tables, Figures and Listings Knowledge of CDISC - SDTM / ADaM is desirableExcellent communication skills in English (German is advantageous)This is a fantastic opportunity to make lasting impression with one of the Top 10 Pharmaceutical companies in the World and have a prestigious client on your CV and could lead to a long-term relationship with this client based on performance.Rate: Up to and#128;650 Per Day (Depending upon experience)Duration: 18 Months (6 Months Extension possible)Location: Near Frankfurt, GermanyStart Date: ASAP  If you are available and interested in this position please contact Vincent Klauser at Real Pharma on + 49 (0) 69 264 89 8400 or email v.klauser(at)real-pharma.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Biostatistician  Near Cologne  6 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF78E9F793F100D18482579F5001FC60D</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Biostatistician-Near-Cologne-6-Months-_1641166.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client are global Pharmaceutical company based near Cologne with multiple offices around the globe and an excellent reputation in the Pharmaceutical industry. They require a Freelance Clinical Trial Biostatistician due to an opening in their Biostatistics department due to a member of staff taking maternity leave for the next 6 months.As a Clinical Trial Biostatistician you will be working on multiple clinical trials for a number of different substances / phases within the drug development lifecycle. Your role will be to provide statistical input into the trial protocol, statistical analysis plan, statistical analyses and reporting on the findings of different clinical trials. Working within a team of statisticians and statistical programmers you will be reporting to the Clinical Program Biostatistician reporting on significant milestones and results within each trial. Experience:-* 5 years + pharmaceutical industry experience as a Biostatistician* Phase II and#150; III experience * Submission experience* Excellent knowledge of different statistical methods* Strong SAS Programming skills* Excellent written and verbal communication skills in English (German advantageous)This is a fantastic opportunity to make lasting impression with one of the Top 10 Pharmaceutical companies in the World and have a prestigious client on your CV and could lead to a long-term relationship with this client based on performance.As a specialist recruiter in Data Management and Biostatistics positions for Pharmaceutical clients in Germany and Switzerland, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.Location:  Near Cologne Duration: 6 months + (extension possible)Rate: NegotiableIf you are interested in this position please contact Vincent Klauser at Real Pharma on + 49 (0) 69 264 898 400 or email v.klauser(at)realstaffing.com for more information.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Manager  Medical Advisor (mw)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5F526B76FCBC545E482579F5001FC618</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Manager-Medical-Advisor-m-w_1641167.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Pharma berand#228;t Unternehmen weltweit bei der Besetzung ihrer Positionen im Pharmabereich. Wir bieten auand#223;ergewand#246;hnliche Jobmand#246;glichkeiten fand#252;r talentierte Fachkrand#228;fte. Profitieren auch Sie von unserem qualifizierten Netzwerk und unserem Know-how.Ab sofort suche ich im Namen eines global agierenden, pharmazeutischen Unternehmens einen Medical Manager / Medical Advisor (m/w):Ihre  Aufgaben umfassen als Medical Manager:and#149;Mitarbeit im Medical Departmentand#149;medizinisch-wissenschaftliche Tand#228;tigkeitenand#149;wissenschaftliche Betreuung nationaler und internationaler Projekte in der klinischen Forschungand#149; Erstellung medizinischer Schulungsunterlagen sowie Schulung der Auand#223;endienstmitarbeiterand#149;Schnittstellenfunktion mit der ZulassungsabteilungIhre Qualifikationen:and#149;Berufserfahrung in der Pharmabrancheand#149;Abgeschlossenes medizinisches Studium, Facharztausbildung von Vorteiland#149;Mehrjand#228;hrige Klinische Erfahrungand#149;Belastbarkeit und Wortgewandtheitand#149;flieand#223;end in Deutsch und EnglischWas Ihnen geboten wird:and#149;and#220;berdurchschnittliche Sozialleistungenand#149;flache Hierarchien und kurze Entscheidungswegeand#149;eigenstand#228;ndiges und verantwortungsvolles ArbeitenFalls Sie sich selbst wiedererkennen und diskret nand#228;here Details erfahren mand#246;chten, dann senden Sie Ihren Lebenslauf an  h.holowaty(at)realstaffing.com oder greifen Sie zum Telefon und kontaktieren Hanna Holowaty.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Control Microbiologist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCCC8927B3D8F41E9482579F5001FC623</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Control-Microbiologist_1641168.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Quality Control Microbiologistand#60;/band#62;and#60;/uand#62;A pharmaceutical company in the San Francisco bay are is looking for a Quality Control (QC) Microbiologist.  The major purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the areaand#146;s supervisor.Quality Control Microbiologist Responsibilities:and#149;Performance and reporting of safety testing for product release, and other related testing.and#149;Compilation and entry of environmental monitoring data. Reviewing of EM Dataand#149;Recording and reviewing of daily monitoring data for laboratory equipment. and#149;Assisting in raw material inspections by performing microbiological testing as requiredand#149;Performing the required testing for protocols.and#149;Revising of Standard Operating Procedure (SOP) as required.Quality Control Microbiologist Requirements:and#149;7 years of pharmaceutical or biotechnology industry experienceand#149;5 years of QC experienceIf you are interested in applying to this job, please reply to this job positing as soon as possible to be considered.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Administrator]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob74DACFDE2FF712DF482579F5001FC62E</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Research-Administrator_1641169.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#149; Maintains overall study accountability, including distribution and reconciliation of all investigational product.and#149; Assists in the preparation of study protocols, site-specific instruction manuals and case report forms, and other study aids for investigational products.and#149; Ensures validity of study information by monitoring and tracking clinical study data to identify/resolve discrepancies and obtain missing data.  Monitoring activities can include both on-site visits with source-data review/reconciliation and remote data monitoring.  and#149; Ensures timely collection of study documentation by obtaining, maintaining and controlling all necessary records and documentation according to corporate and departmental procedures and regulations.and#149; Ensures proper product supply, accountability and storage during assigned clinical studies and resolves any discrepancies during inspections of clinical site device accountability records and storage facilities.and#149; Coordinates collection of source documents for trial adverse experiences and drives the clinical event safety process towards adjudication of events in coordination with adjudication bodyand#149; Contributes to the SOPs for regulatory and clinical functional groups.and#149; Ensures appropriate communication processes are established within and across functional groups. and#149; Works in accordance with internal quality system procedures and ensures study and site compliance with protocol and regulatory policies.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Validation Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC337C295264C5353482579F5001FC639</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Software-Validation-Specialist_1641170.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Background Informationand#60;/band#62;This position will support various functional groups in preparing documentation that follows our internal Operating Procedure for Validation of Quality System Applications.  This includes, but is not limited to, IT, QA, Doc Control, Manufacturing, Rand#38;D, etc. The Consultant needs to be able to understand the processes described and assist the business process owners in preparing documentation that is required by this process.  and#60;band#62;Essential Duties and Responsibilitiesand#60;/band#62;and#149;Review process documents for compliance to requirementsand#149;Attend meetings with cross-functional project members to prepare required documentsand#149;Provide expertise in the process for Validation of Quality System application softwareand#149;Provide expertise in and assure preparation of complete and accurate documents that support the validation of key aspects of a given software package that will require validationand#149;Interface with the appropriate Technical and QA personnel to obtain current and ongoing process activitiesand#149;Provide guidance in structuring prepared documents for compliance and traceability for future use and understanding]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Responsable Médical Senior (hf)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob08453C513C79AE94482579F5001FC644</referencenumber>
<City><![CDATA[Ile]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Responsable-M-and-amp-SHARP233dical-Senior-h-f_1641171.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Rejoignez un laboratoire pharmaceutique international qui recherche un Responsable Mand#233;dical Senior (h/f).Votre challenge:Rattachand#233;(e) directement au Prand#233;sident France, vous and#234;tes chargand#233; de dand#233;velopper la division mand#233;dicale en France de ce groupe international.  Vos missions:- Contribuer au dand#233;veloppement stratand#233;gique mand#233;dical du groupe sur les zones Moyen-Orient - Afrique- Dand#233;velopper et gand#233;rer le rand#233;seau de KOL des diffand#233;rents domaines thand#233;rapeutiques concernand#233;s - Former les diffand#233;rents partenaires sur les produits du groupe- Valider les documents promotionnels- Organiser des rand#233;unions professionnelles et scientifiques, afin dand#146;apporter land#146;information mand#233;dicale autour des produits- Participer aux congrand#232;s nationaux et internationaux Votre profil:- Vous and#234;tes mand#233;decin, Directeur Mand#233;dical avec une expand#233;rience confirmand#233;e en mand#233;dico-marketing (environ 10 ans) -Votre expand#233;rience dans diffand#233;rents domaine thand#233;rapeutiques tand#233;moigne de votre adaptabilitand#233; et votre flexibilitand#233;-Vous avez idand#233;alement une expand#233;rience and#224; land#146;and#233;tranger ou and#224; land#146;export-Vous and#234;tes autonome et force de proposition et vous souhaitez rejoindre une structure qui donne les moyens dand#146;avancer-Vous maand#238;trisez parfaitement land#146;anglais, la connaissance de land#146;arabe est un plusLocalisation : rand#233;gion parisienneDate de dand#233;marrage : au plus tand#244;tEnvoyez-moi dand#232;s maintenant votre CV sous format Word ou nand#146;hand#233;sitez pas and#224; transmettre cette offre autour de vous. NB : Sans nouvelles de ma part dans les 3 semaines suivant rand#233;ception de votre candidature, veuillez considand#233;rer que votre candidature nand#146;aura pas and#233;tand#233; retenue pour ce poste. Je me permets toutefois de garder votre candidature pour une opportunitand#233; similaire and#233;ventuelle. http://fr.realstaffing.com/fr/page/pharma_sector/]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Bioinformatics Scientist III  SF Bay Area  Long Term Contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB2046988F6E59305482579F5001FC64F</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Bioinformatics-Scientist-III-SF-Bay-Area-Long-Term-Contract_1641172.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SF Bay Area DNA Sequencing Start-Up is urgently seeking a high level Bioinformatics Consultant to work on an exciting project.  This is a long-term consulting position, with the aim to eventually go permanent.  Candidates who have these qualifications will be considered:- MUST have a PhD in Biology or other Biological Science concentration.  This position requires a deep understanding of science, therefore candidates are required to demonstrate a publication record.  - 7 - 10 years of experience in the Bioinformatics Space.  At least 5 of these years must be within the Pharmaceutical/Biotechnology industry.- Working knowledge of the following technologies: mySQL, R, Perl, Python, Matlab, C++.  This is not a heavy coding position, but candidates should be able to work with these programs.- Ability to work in a diverse working space, this candidate will be a liaison between several groups.- Dynamic and ethusiastic attitude are a must - while the company mission and objectives are clear, this is a start-up environment and candidates must be able to wear many hats]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director, Analytical Development and Quality Control]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob85350CBDD32DE138482579F5001FC65C</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Associate-Director-Analytical-Development-and-Quality-Control_1641173.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Associate Director, Analytical Development and Quality Controland#60;/band#62;and#60;/uand#62;A pharmaceutical company in the San Francisco bay area is looking for an Associate Director, Analytical Development and Quality Control to join their team.  This is a contract to hire opportunity and a great way to get your foot in the door with a growing, exciting company.  The successful candidate will provide leadership for analytical development and testing programs. You will oversee day-to-day laboratory and quality control operations as well as additional responsibilities that include the following:and#149;  Oversee and lead client programs that require use of novel and routine analytical methods intended for characterization and stability/release testing of products across all development phases.and#149;  Coordinate with QA to ensure that cGMP testing is performed in compliance with regulatory requirements.and#149;  Direct, develop and optimize analytical methods for protein characterization and quality methods.and#60;band#62;Associate Director, Analytical Development and Quality Control:and#60;/band#62;The ideal candidate will have a Ph.D. with 6+ years of hands-on, laboratory biochemistry, analytical chemistry, and/or protein chemistry laboratory experience, and 3+ years experience supervising technical teams in industry. In-depth knowledge and experience with cGMP compliance requirements (FDA, EMEA) in the biotech industry is a must.To apply to this position, please reply to this job positing with your resume.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Ingénieur R&D expérimenté en électronique analogique et numérique]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB299E7A13FF13039482579F5001FC667</referencenumber>
<City><![CDATA[Ile]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Ing-and-amp-SHARP233nieur-R-and-amp-SHARP38D-exp-and-amp-SHARP233riment-and-amp-SHARP233-en-and-amp-SHARP233lectronique-analogique-et-num-and-amp-SHARP233rique_1641174.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Sociand#233;tand#233; franand#231;aise productrice de dispositifs mand#233;dicaux de haute technologie, spand#233;cialisand#233;e dans le recueil et le traitement de signaux dans le domaine de la cardiologie.Le poste :Au sein du dand#233;partement Rand#38;D vous and#234;tes en charge de la conception et de land#146;architecture des composants and#233;lectroniques. Vous and#233;voluez dans un environnement and#224; forte contraintes techniques (dispositif de petite taille, de basse consommation and#233;nergand#233;tique,and#133;) et rand#233;glementaires (environnement mand#233;dical, ISO 13485, ISO 9001-2000)Vous and#234;tes en charge de tout le cycle de vie du produit : de la conception and#224; land#146;industrialisation ainsi que le service aprand#232;s-venteLe profil :De formation and#233;lectronique (BAC+5) vous band#233;nand#233;ficiez dand#146;une expand#233;rience professionnelle dand#146;au moins 5 annand#233;es dans un dand#233;partement Rand#38;D (Electronique)Vous avez dand#146;excellentes compand#233;tences en and#233;lectronique analogique ET numand#233;rique et vous avez une longue expand#233;rience de travail avec des microcontrand#244;leursVous and#234;tes communiquant, vous and#234;tes passionnand#233; par le dand#233;veloppement and#233;lectronique et vous avez un bon niveau dand#146;AnglaisEnvironnement technique :Temps rand#233;el embarquand#233;Langage C, assembleur sur microcontrand#244;leurs (type : MSP430)Fonctions logiques pand#233;riphand#233;riques associand#233;esAcquisition et traitement de signaux physiologiques (normes CEM, IEC 60601), TCP/IP, bluetooth, Wifi, GSM, GPRS, USB and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Distriktleiterin  Süddeutschland  Spezialaußendienst  BayernBaden]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob425DC86AF576E5A2482579F5001FC670</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Distriktleiter-in-S-and-amp-SHARP252ddeutschland-and-amp-SHARP150-Spezialau-and-amp-SHARP223endienst-and-amp-SHARP150-Bayern-Baden_1641176.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Einer meiner Kunden, ein stark expandierendes Biotech-Unternehmen, will seinen Expansionskurs fortfand#252;hren und sucht einen Distriktleiter/in fand#252;r Sand#252;ddeutschland.Ihre Aufgabe ist die adand#228;quate Unterstand#252;tzung des Vertriebsleiters Nord und der Aufbau einer eigenen Sales Force, um die relevanten Gebiete bundesweit fand#252;r das Unternehmen optimal abzudecken.Sie arbeiten im Bereich der Orphan Drugs und stellen sich interessanten Aufgaben.Als ideale(r) Kandidat/in kand#246;nnen Sie folgende Erfahrungen nachweisen:and#149; Erfahrung als Vertriebsleiter in einem Pharma and#150; oder Biotech-Unternehmenand#149; flieand#223;ende Deutsch -  und Englischkenntnisseand#149; Erfahrung mit der Fand#252;hrung von Fachkrand#228;ftenand#149; Kommunikationsstarkand#149; Kenntnisse and#252;ber die Gesundheitspolitikand#149; Organisations- und Zeitmanagementand#149; Idealerweise haben Sie Erfahrung im Bereich Orphan Drugs oder PulmonaryWas halten Sie davon and#150; das klingt doch interessant?Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich gerne an Herrn Elyas Bozan wenden. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent Senior Process Validation Engineer San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob199FA14E625F4AE8482579F5001FC67C</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-Senior-Process-Validation-Engineer-San-Diego_1641177.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client in San Diego has an urgent requirement for a Senior Process Validation Engineer with 6 years experience in the Pharmaceutical Industry with the following qualifications:Act as Process Validation subject matter expert for resolution of deviations, assessment of change orders and other quality system actionsOversee/execute selected studies and protocols for processes and systems.Write selected studies, plans, protocols, and reports for processes and systemsQualifications:Education/Experience:BS degree in a scientific discipline with at least 6 years of experience, orMS degree with at least 4 years of related experience.Required Skills/ Knowledge:and#149;Management of complex validation projectsand#149;In depth, working knowledge of 2004 FDA Aseptic Process Guidance for Industryand#149;Solid background and experience with GMPand#146;sand#149;In depth working knowledge of 2011 FDA Process Validation Guidance for Industryand#149;Experience implementing Process Validation Programand#149;Quality Risk Management conceptsThis is an extremely attractive offer that will not be available for long. If interested please send your resume immediately.Keywords: PROCESS VALIDATION, PROCESS ENGINEER, VALIDATION ENGINEER, GMP, DEVIATIONS, CHANGE ORDERS, FDA, QULAITY RISK MANAGEMENT]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Executive: £35k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB1DB4171E3F2EA8F482579F5001FC689</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Executive:-and-amp-SHARP16335k_1641178.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;and#60;/band#62;Regulatory Affairs Executive: and#163;35k+ Location: Commutable from London, Harrow, Uxbridge, St Albans, Slough, Maidenhead Job Purpose: To be responsible for the effective coordination and supervision of the required work flow within the department to ensure effective and efficient maintenance of existing licences and new applications.Main duties and responsibilities:and#149;Preparation of licence applications and leaflet updates for both MHRA and EMEAand#149;Monitoring pending applications to ensure rapid processing and responding to queries from the licensing authorityand#149;Maintenance of granted licences including variations and renewalsand#149;Preparation of internal batch control documentation including design of components for internal and external printing (cartons, labels and patient leaflets) and updating as requiredand#149;Implementation of Batch Production Records and updating electronic recordsand#149;Liaison with other departments including production and quality assurance and PV departmentsand#149;Advising senior management on trade mark issuesand#149;Assessing the applicability of the and#147;Specific Mechanismand#148; to potential productsand#149;Maintenance of appropriate databases to record licence status, trade mark status and componentsand#149;Direction, development and training of staffand#60;uand#62;and#60;band#62;Education: and#60;/band#62;and#60;/uand#62;You must have a degree in life sciences as a minimum If you are keen to find out more email me your update C.V at n.hopkins(a)realstaffing.com or call 02077587311  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. Bioinformatics SW Engineer  Contract  SF Bay Area]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC445F78BE6FD48F6482579F5001FC695</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Bioinformatics-SW-Engineer-Contract-SF-Bay-Area_1641179.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SF Bay Area Biotechnology Company, is seeking to bring on a Sr Bioinformatics SW Engineer to their team.  You will be focusing on developing developing the companys DNA sequencing product and working to bring this to market.  The ideal candidate would have the following qualifications:- Minimum of an MS, preferrably a PhD, in Biology, Computer Science, Statistics, Biostatistics or other Life Science background- 4-7 years of experience working on related projects (3 years must be in industry)- Technical skills: Python, Java, Perl, mySQL, Machine learning, SOA, statistical learning, R, Matlab, Web Services.  Must be able to work in a Linux environment.- Command of algorithm development and database design- Ability to be forward thinking and solve problems related to software development- Excellent communication skills and enthusiasm - this particular group is passionate about Genomics and Personalized Medicine and would like their new member to share this as well.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4D11BDBAA151FB97482579F5001FC6A0</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-gesucht_1641180.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Wir suchen ab sofort einen Regulatory Affairs Manager fand#252;r ein Medizintechnik-Unternehmen in and#214;sterreich. Mein Kunde ist in seinem Segment Marktfand#252;hrer und wand#228;chst zurzeit sehr stark. Das sollten Sie mitbringen:and#149;Erfolgreich abgeschlossenes technisches oder vergleichbare Ausbildungand#149;Nachweisbare, mehrjand#228;hrige Erfahrung im Bereich der Zulassungenand#149;Reisebereitschaftand#149;Verhandlungssichere Deutsch- und Englischkenntnisse in Wort und Schriftand#149;Motivierte, teamfand#228;hige und kommunikationsstarke MitarbeiterIhre Aufgaben:and#149;Erstellung und Pflege der zulassungsrelevanten Unterlagenand#149;Kontakt und Verhandlung mit den relevanten nationalen und internationalen Behand#246;rden and#149;Koordination mit den jeweiligen Land#228;ndervertretungen bei Zulassungen auand#223;erhalb des europand#228;ischen RaumsWenn Sie auf der Suche nach einer neuen Herausforderung in einem internationalen Unternehmen sind and#150; dann bin ich Ihr richtiger Ansprechpartner.Bitte kontaktieren Sie mich, gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[International Area Sales Manager  Pharma  Bayern!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9AFD5D8E833A160D482579F5001FC6B5</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/International-Area-Sales-Manager-and-amp-SHARP150-Pharma-and-amp-SHARP150-Bayern_1641181.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Sind Sie auf der Suche nach einer internationalen Position im Vertrieb? Wollen Sie als Area Sales Manager das B2B and#150; Business mit den Partnern in den Ihnen zugewiesenen Regionen vorantreiben? Sollten diese Faktoren relevant sein fand#252;r Sie, dann haben wir hier die richtige Vakanz.Zu Ihren wichtigsten Aufgaben zand#228;hlt die enge Zusammenarbeit mit den Distributoren in der von Ihnen betreuten Region. Sie betreuen neben den Bestands- auch Neukunden und unterstand#252;tzen diese im Bereich Marketing, Prozesse der Produktneueinfand#252;hrung. Sie sprechen Empfehlungen fand#252;r die strategische Ausrichtung aus, analysieren die Potentiale fand#252;r die Erschlieand#223;ung neuer Mand#228;rkte und sind auch fand#252;r die Budgetplanung verantwortlich. Als International Area Sales Manager sind Sie in der Lage, geeignete Vertriebspartner fand#252;r die eigenen Produkte zu gewinnen.Um dieser Aufgabe gerecht zu werden, sollten Sie folgendes mitbringen:and#149; Vertriebs and#150; und Marketingerfahrungand#149; Die Zusammenarbeit mit Distributoren ist Ihnen bestens bekanntand#149; B2B-Erfahrungand#149; Flieand#223;ende Deutsch- und Englischkenntnisse sind notwendigand#149; Idealerweise haben Sie Berufserfahrung innerhalb der Pharmaindustrie gesammelt Was fand#252;r ein Unternehmen erwartet Sie?Mein Kunde ist ein weltweittand#228;tiges Unternehmen und konzentriert sich unter anderem auf die Bereiche Respiratory und Gynaecology. Wenn wir Ihr Interesse geweckt haben, dann freuen wir uns auf Ihre Bewerbung. Gerne kand#246;nnen Sie sich als Junior-Fachkraft ebenfalls bewerben.Bei Fragen wenden Sie sich bitte an Herrn Elyas Bozan. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Engineer Sr  Irvine  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDC79B7DF00FBCC27482579F5001FC6C2</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Assurance-Engineer-Sr-Irvine-URGENT_1641182.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has an urgent need for a Senior Quality Engineer with the following qualifications and skills;and#149;Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), EMEA, Health Canada, ANVISA and other regulatory requirements in a regulated manufacturing environment and#149;Monitors activities in key areas for compliance to standards, and identifies opportunities for improvement and#149;Researches and recommends improvements in production and#149;Manages the nonconformance/deviation investigation process and#149;Quality review of Facility/ Equipment Work orders and#149;Quality approval of change controls and#149;Quality review and approval of Qualification, Validation and all other GMP documents and#149;Provides quality assurance support for site and corporate project teams and#149;Analyzes data from production and laboratories, and reports deviations and#149;Helps direct junior level QA Engineering staff in completion of assignments and#149;Provide knowledge support during third party audits/regulatory audits and#149;Performs related duties as assignedDesired Skills and#38; ExperienceQUALIFICATIONS:   The ideal candidate will have:   KNOWLEDGE OF: and#149;Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements in a regulated manufacturing environment and#149;OSHA, FDA, EPA, Health Canada, ANVISA,EMEA, DEA, AQMD and other regulatory and safety compliance guidelines and#149;Root Cause Analysis and Deviation/Non-Conformance Investigations and#149;Applied cGMPs and#149;Auditing techniques in a regulated environment and#149;Applied statistics and trend analysis and#149;Change Control Program and#149;Solid Dosage Pharmaceutical manufacturing, packaging, suppliers, raw materials and products processes and#149;Change Control Program and#149;Technical writing, English usage, spelling, grammar and punctuation and#149;Equipment and Facilities qualification and#149;Product and Process Validations and#149;Engineering and business computer systems and software applications (TrackWise, JDE, SAP, LiveLink, LIMS, JMP) and#149;Project management and#149;Laboratory equipment and testing]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer in Mecklenburg Vorpommern gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2B47BA758EAA812A482579F5001FC6CD</referencenumber>
<City><![CDATA[Mecklenburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-in-Mecklenburg-Vorpommern-gesucht_1641183.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein interessantes Medizintechnikunternehmen in Mecklenburg-Vorpommern sucht einen Quality Engineer zur Erweiterung des Qualitand#228;tteams. Ihre Aufgabengebieteand#149;Herstellung von Produkten/Komponenten Risikoanalysen und Qualitand#228;tsplanungand#149;Prand#252;fung der Qualitand#228;tsstandards in Bezug auf Verbesserungspotentiale and#149;Maand#223;nahmen, zur Verbesserung von Mand#228;ngel (intern und extern) and#149;Prand#252;fung der Einhaltung der Qualitand#228;tsnormen in jeder Fertigungsphase and#149;Arbeits- und Verfahrensanweisungenand#149;Organisation des kontinuierlichen Verbesserungsprozessesand#149;Prozesscontrolling der Verbesserungsprojekteand#149;Dokumentation der Prand#252;fergebnisse und das Erstellen der Vorgabedokumenteand#149;Produktionsaudits und QM-Checks and#149;Qualitand#228;tsgesprand#228;che mit Lieferanten and#149;Mitwirkung bei der Auswahl neuer Lieferanten and#149;Qualitand#228;tsschulungen der Mitarbeiter Sie bringen einen Abschluss als Ingenieur FH/TU in der Fachrichtung Maschinenbau oder Verfahrenstechnik mit und besitzen Kenntnisse in der Anwendung von Qualitand#228;tstechniken. Sie haben bevorzugt mehrjand#228;hrige fachtechnische Berufserfahrung sowie Erfahrungen im Qualitand#228;tsmanagement. Eine Ausbildung/Zertifikate im Qualitand#228;tsmanagement (z. B. Qualitand#228;tsmanager) sind von Vorteil. Der sicherer Umgang mit MS Office sowie SAP-Kenntnisse und Kenntnisse mit Statistiktools (z. B. Minitab) sind wand#252;nschenswert. Ebenfalls weisen Sie gute Statistikkenntnisse sowie Englisch-Kenntnisse in Wort und Schrift auf.Wenn Sie die Rolle des and#252;berzeugenden land#246;sungsorientierten Moderator and#252;bernehmen kand#246;nnen und and#252;ber eine selbstand#228;ndige Arbeitsweise verfand#252;gen, freue ich mich auf Ihre Bewerbung. Agnes Wydra/ a.wydra (at)realstaffing (dot)com+49 (0)69 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs und Quality Manager gesucht  Baden Württemberg]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBC31CBAACE2924C7482579F5001FC6D9</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-und-Quality-Manager-gesucht-and-amp-SHARP150-Baden-W-and-amp-SHARP252rttemberg_1641184.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein innovatives Unternehmen der Medizintechnik suche ich einen Regulatory Affairs und Quality Manager. Das Unternehmen ist auf Wachstumskurs und Vorreiter in neuen Technologien. Sie bringen Persand#246;nlichkeit, Durchsetzungsvermand#246;gen und einen ausgeprand#228;gten Teamgeist mit? Dann lesen Sie weiter.Ihre Aufgaben:and#149;Kommunikation mit zulassungsrelevanten Behand#246;rden und Organisationenand#149;Pflege des Qualitand#228;tmanagementsand#149;Management von Zertifizierungen und anderen externen Auditsand#149;Erstellung technischer Dokumentationenand#149;Betreuung des Produktentstehungsprozessesand#149;Enge Zusammenarbeit mit allen Abteilungen des UnternehmensIhr Profil:and#149;Abgeschlossenes technischen Studium (Schwerpunkt Medizintechnik)and#149;2-3 Jahre Berufserfahrungen im Bereich der nationalen und internationalen Zulassung fand#252;r Medizinprodukteand#149;Erste Erfahrungen im Qualitand#228;tsmanagementand#149;Kenntnisse von relevanten Normen, Gesetzen und Regularienand#149;Sehr gute Deutsch- und EnglischkenntnisseSie sind an dieser anspruchsvollen und spannenden Herausforderung interessiert and#150; dann bin ich Ihr richtiger Ansprechpartner. Zand#246;gern Sie nicht und kontaktieren Sie mich!Ihre Ansprechpartnerin: Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent Principal Quality Engineer 5yrs exp  San Diego, excellen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE89D486A8AE538E5482579F5001FC6E5</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-Principal-Quality-Engineer-5yrs-exp-and-amp-SHARP150-San-Diego-excellen_1641185.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Job DescriptionPerforming failure and trend Analysis, investigations and communicating compliance problems between teams. The position will also be responsible for documentation, and compliance procedures, implementing CAPAs, and reviewing NMCRs. Familiarity with GMP and ISO3485, or medical instruments. Six Sigma problem solving, and certified PM is a plus.This is a fantastic opportunity for a long term contract with a well established pharmaceutical company. It is an urgent role, so if you would be a good fit for the position please email me your resume as soon as possible. Key Words: QA, Pharmaceutical, GMP, failure Analysis, CAPA, compliance documentation, Six Sigma]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Associate, very urgent requirement, Geneva]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA13F653388E3A5A5482579F5001FC6F1</referencenumber>
<City><![CDATA[Geneva]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Research-Associate-very-urgent-requirement-Geneva_1641186.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An international pharma company with a fantastic work environment and locations worldwide is looking for a Clinical Research Associate in Geneva. The position offers the opportunity for involvement with studies in all phases.The unique Swiss landscape, culture and mentality will definitely enrich you whilst the unparalleled quality of life allows you to enjoy your free time skiing and hiking in the mountains.The clinical operation team wants to expand their team with a highly motivated Clinical Research Associate, who supports the team and brings a positive outlook. The multi-cultural team is very open with development opportunities available to someone aspiring to further their career.As an employee in the clinical research field you will be responsible for preparing documents and protocols, controlling the trial master file, supporting the clinical team in relation to studies, communication with relevant people in the clinical operation environment, developing of monitoring plans e.g. EC-submissions for the studies. The Candidates requirements are:and#149;1.5 year work experience as a CRA or 1 year as a CTA in medical devices or in pharmaceutical or biotech or generic drug companyand#149;A degree in clinical research or in a related field of study and#149;The candidate should speak fluent German and English or be fluent in Italian or in French.If you like to get more information on this position, then donand#146;t hesitate to contact Nadja Beckert at Real Pharma as soon as possible on 0041 (0) 43 508 097 2 or call me on n.beckert(at)realstaffing.com. This position is one of 25 positions, which I hold at the moment. Further if this position doesnand#146;t suit to you, please let me know and we can also discuss other positions in Switzerland.Schweiz, Luzern, Zand#252;rich, klinische Studien, clinical Trial, CRA, CTA, Pharmabereich, Switzerland, klinische Forschung, klinische Untersuchungen, Clinical Trial Assistant, klinische Mitarbeiter, SCRA, Senior CRA, Principal CRA, Kanton Zand#252;rich, Clinical Operation, Nadja Beckert, Studienbegleitung, Clinical Data Associate, Clinical Research Associates, Clinical Trial Manager, Clinical Studies, Study Managers, Klinisches Monitoring, Monitoring, CRO, CRA, Senior CRA, Senior CRO, Director Clinical Research, Head of Medical Studies, Head of Clinical Research, Clinical Project Managerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Auditorin oder Expertein für Medizinprodukte Raum Frankfurt am Main]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob03E19073177A06EC482579F5001FC6FE</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Auditor-in-oder-Experte-in-f-and-amp-SHARP252r-Medizinprodukte-Raum-Frankfurt-am-Main_1641187.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein interessantes Medizintechnikunternehmen in Hessen sucht eine/n Auditor/in oder Experte/-in fand#252;r MedizinprodukteZu Ihren Aufgabengebieten gehand#246;rt als Auditor/in die Bewertung von Qualitand#228;tsmanagementsystemen sowie als Fachexperte/-in das Bewerten von technischen Produktdokumentationen sowie das agieren im Auditteam. Fand#252;r diese verantwortungsvolle Aufgabe bringen Sie gute Erfahrung als Auditor fand#252;r QM-Systeme EN ISO13485,  nach EN ISO 9001 und Technischen Dokumentationen oder Erfahrung in der Entwicklung, Prand#252;fung oder klinischen Anwendung von Medizinprodukten und/oder Software mit. Sie haben Interesse an der aktiven Mitarbeit bei der Entwicklung von strategisch interessanten Mand#228;rkten und Dienstleistungen sowie an der Kundenbetreuung. Flexibilitand#228;t und Reisebereitschaft sowie gute Kenntnisse der englischen Sprache in Wort und Schrift bringen sie verstand#228;rkt mit. Von Vorteil ist, wenn sie and#252;ber Fachwissen zu den Anforderungen an die Konformitand#228;tsbewertung von Medizinprodukten sowie im Bereich Prand#252;fung, Bewertung oder Erstellung von technischen Produkt- und Prozessdokumentationen in der Medizintechnik verfand#252;gen.Sind Sie bereit fand#252;r eine neue Aufgabe in einem aufstrebenden sowie wachsenden Unternehmen? - Dann bewerben Sie sich oder kontaktieren Sie mich direkt unter folgenden Kontaktdaten:a.wydra(at) realstaffing.com Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Systems Specialist  Internal Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6F98172F986BFBD0482579F5001FC70C</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Quality-Systems-Specialist-Internal-Auditor_1641188.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is an international company from NRW near Kand#246;ln. Itand#180;s a very innovated medical device company who is looking for a Senior Quality System Specialist and internal Auditor to improve their production department.Job Qualifications and#149;BA/MS plus several years experience in related or equivalent industry and#149;FDA Quality System Requirements: ISO 13485, ISO 9001and#149;ANSI/AAMI SW 68, and ISO 14971 risk management standardsand#149;Six Sigma, M3K, etc. and#149;Background in one or more of the following areas desiredand#149;Familiarity with radiation therapy helpfuland#149;excellent verbal and written communication skillsand#149;Interacting with all levels of managements, co-workers, and regulatorsand#149;english fluent for international travels and#149;Regulatory AffairsJob Description and#149;FDA Quality Systems Regulation (QSR), ISO 13485, ISO 9001 and#149;Writing SOPs, work instructions, quality and control plans etc.and#149;CAPA process and#149;internal audits and Compliance with audit programsand#149;reporting results to managementand#149;Plan and perform support activities/ lead and coordinate site activities and#149;validation protocols and test reportsand#149;FMEA/FTAand#149;Work closely with different departmentsand#149;Assist with FDA inspectionsFor further information about this great opportunity, please e-mail or call Agnes Wydra (Quality Management Recruitment Consultant) at Real Pharma on 0049 (0) 69 26 489 8400.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Manager nahe Osnabrück gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob69FB0EC77F2EB0BD482579F5001FC71A</referencenumber>
<City><![CDATA[Niedersachsen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Manager-nahe-Osnabr-and-amp-SHARP252ck-gesucht_1641190.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein deutsches  Familienunternehmen mit internationalem Umfeld in der Medizinbranche, sucht nahe Osnabrand#252;ck einen zielstrebigen Qualitand#228;tsmanager.Ihr Profil:-Erfolgreich abgeschlossenes Studium der Naturwissenschaften, Pharmazie, Ingenieurwissenschaften oder vergleichbare Qualifikation-Qualitand#228;tsmanager/in (DQS, EFQM-Modell)-Berufserfahrung in einer vergleichbaren Tand#228;tigkeit-Interpretation und Umsetzung von ISO 13485 / GMP-Anforderungen-Projekterfahrung im QM-Umfeld (Prozessentwicklung, Design Transfer, Change Control, CAPA) -Kenntnisse im Qualitand#228;tsmanagement fand#252;r Medizinprodukte und Arzneimittel -Sehr gute Englischkenntnisse in Wort und SchriftIhre Aufgaben:-Sicherstellung der regulatorischen Compliance-Life Cycle Management Prozesses nach GMP-Richtlinien, ISO 9001, ISO 13485, MDD und 21 CFR 820, 210, 211-Planung, Umsetzung, Weiterentwicklung, and#220;berwachung und Steuerung des Qualitand#228;tsmanagements und der Prozessorganisation im Qualitand#228;tsmanagement-Planung, Umsetzung, and#220;berwachung und Weiterentwicklung von Prozessen ( z.B. Change Control)- Steuerung des Risikomanagement-Prozesses- Eigenverantwortliche Durchfand#252;hrung von ProjektenWenn Sie diese spannende Stelle anspricht und Sie dazu eine hohe Eigenmotivation, ein ausgeprand#228;gtes Verstand#228;ndnis fand#252;r komplexe Vorgand#228;nge sowie ein souverand#228;nes Auftreten mitbringen, freue ich mich auf Ihre Bewerbung unter folgenden Kontaktdaten: a.wydra (at) realstaffing.com / Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Validierungsingeneur in Niedersachsen gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDB8240A4901A5E73482579F5001FC725</referencenumber>
<City><![CDATA[Niedersachsen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Validierungsingeneur-in-Niedersachsen-gesucht_1641191.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein interessantes Unternehmen in der Medizinbranche, sucht fand#252;r den Bereich QM in Niedersachsen einen Validierungsingeneur.Sie bringen ein erfolgreich abgeschlossenes Studium der Naturwissenschaften, Ingenieurwissenschaften, Pharmazie, oder vergleichbare Qualifikation mit.Aussagekrand#228;ftige Kenntnisse im Bereich der Qualifizierung von Anlagen sowie der Validierung von Prozessen, Prand#252;fmethoden und Software im GMP-Umfeld liegen vor.Erfahrung im Bereich Arzneimittelprand#252;fung oder Arzneimittelherstellung sowie in der Herstellung von sterilen Land#246;sungen, insbesondere fand#252;r Reinraumklassen gemand#228;and#223; Annex 1 des EG-GMP-Leitfadens sind gegeben. Ebenso bringen Sie Kenntnisse mit der Interpretation regulatorischer Anforderungen gemand#228;and#223; 21 CFR 820, cGMP, ISO 13485 und MPG sowie Projektmanagementerfahrung mit.Zu Ihren Aufgaben gehand#246;rt:-Planung, Umsetzung, Monitoring und Reporting aller Validierungs- und Qualifizierungsaktivitand#228;ten: fand#252;r neu zu beschaffende Produktionseinrichtungen inklusive Erstellung von Qualifizierungs- und Validierungspland#228;nen sowie der Validierungsberichte.sowie fand#252;r bestehende Produktionseinrichtungen inkl. ggf. notwendiger Revalidierungsmaand#223;nahmen nach GMP-Richtlinien, ISO 9001, ISO 13485, MDD und 21 CFR 820, 210, 211.Sie fand#252;hren Schulungen zu Themen der Qualifizierung und Validierung durch und erstellen Lastenheften. Ebenfalls wirken Sie bei der Erstellung und Durchfand#252;hrung von Prozessrisikoanalysen und  Prozessfand#228;higkeitsuntersuchungen mit.Wenn Sie diese interessante Stelle anspricht und Sie ein ausgeprand#228;gtes Verstand#228;ndnis fand#252;r komplexe Vorgand#228;nge, sowie ein eingenstand#228;ndiges und wissenschaftlich-strukturiertes Arbeiten mitbringen, freue ich mich auf Ihre Bewerbung unter folgenden Kontaktdaten: a.wydra (at) realstaffing.com / Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Projektleiter Qualifizierung und Validierung nahe Münster gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB1F11F1F44C4D6A3482579F5001FC733</referencenumber>
<City><![CDATA[Niedersachsen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Projektleiter-Qualifizierung-und-Validierung-nahe-M-and-amp-SHARP252nster-gesucht_1641192.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde, ein solides Unternehmen in der Medizinbranche, sucht fand#252;r seine Abteilung QM nahe Mand#252;nster einen motivierten Projektleiter Qualifizierung und Validierung.Zu ihren Aufgabengebieten gehand#246;rt die Projektplanung, Umsetzung, Monitoring und Reporting aller Validierungs- und Qualifizierungsaktivitand#228;ten fand#252;r neu zu beschaffende Produktionseinrichtungen nach GMP-Richtlinien, ISO 9001, ISO 13485, MDD und 21 CFR 820, 210, 211. Die Qualifizierungs- und Validierungspland#228;ne, die Validierungsberichte sowie das Mitwirken bei Erstellung von Lastenheften. Die Erstellung und Durchfand#252;hrung von Prozessfand#228;higkeitsuntersuchungen und Prozessrisikoanalysen. Sie bieten Projektunterstand#252;tzung zur Sicherstellung der regulatorischen Compliance beim Aufbau neuer Produktionslinien sowie bei Product Life Cycle Management-Prozessen.Sie bringen ein erfolgreich abgeschlossenes Studium der Naturwissenschaften, Ingenieurwissenschaften oder vergleichbare Qualifikation, Berufserfahrung in einer vergleichbaren Tand#228;tigkeit sowie Projekterfahrung im QM-Umfeld mit. Kenntnisse im Qualitand#228;tsmanagement fand#252;r Medizinprodukte und Arzneimittel sind wand#252;nschenswert. Sehr gute Englischkenntnisse in Wort und Schrift, eine hohe Eigenmotivation sowie ausgeprand#228;gtes Verstand#228;ndnis fand#252;r komplexe Vorgand#228;nge sind Ihr Steckenpferd. Eigenstand#228;ndiges, wissenschaftlich-strukturiertes Arbeiten sowie souverand#228;nes Auftreten rundet ihr Profil ab.Hat Sie diese Stelle angesprochen? Dann freue ich mich auf Ihre Bewerbung unter folgenden Kontaktdaten: a.wydra (at) realstaffing.com / Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Biostatistician   Early Phase Oncology  Growing BioPharma]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8281322328A192AF482579F5001FC740</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Biostatistician-Early-Phase-Oncology-Growing-BioPharma_1641193.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Position Senior / Principal Level BiostatisticianTherapeutic area - Oncology (early phase)Location - Greater BostonCompany size - approx 150 - 200Company profile:A Biopharmaceutical company focused on the discovery and development of transformational medicines for complex disease, with an initial focus on cancer.  With 5 compounds in oncology clinical trials and a strong pipeline that is expected to produce several more clinical development candidates in the near future this company are an exciting environment for Biostatisticians with early phase oncology experience who are looking to be part of a growing leading edge organisation who will be making a positive difference to the treatment of future cancer patientsThe Senior  / Principal Biostatistician will be working with a cross functional program team as the statistical lead, responsible for statistical activities across multiple studies, and reporting to the program medical director. The ideal candidate is a good communicator, high-energy, self-motivated, and forward thinking. Experience working in oncology development is preferred, but not required. Job Responsibilities:Provide leadership and guidance as the statistical expert on a cross functional program team Represent statistical issues with external parties including regulatory agencies and corporate partners Work collaboratively with internal and external (e.g. CRO) team members to coordinate the planning and execution of biostatistics deliverables Work with data management personnel in the preparation of datasets that are of high quality and in usable format Apply statistical expertise to ensure optimal clinical trial designs, analysis methods and data displays Be accountable for all statistical aspects of protocols and regulatory submissions Contribute to the development of statistical approaches and support for biomarker analysis and translational research.Provide requirements to SAS Programmers to facilitate efficient and effective programming Be responsible for quality assurance of data produced, the validity of the reported results and their statistical interpretation Participate in the establishment of processes and standards for the generation and reporting of data Requirements:PhD / MS in statistics or related discipline with at least 5 (7) years of experience in the pharmaceutical or biotech industry Demonstrated ability to effectively contribute to the statistical aspects of clinical protocol design, data interpretation, review and reporting of results for multiple studies and projects Practical experience with application of advanced statistical methodologies to clinical trial design/analysis and with regulatory reporting/submissions Experience managing outsourced biostatistical services Proficiency with statistical software tools such as SAS, S-Plus, R, EAST Familiarity with regulatory requirements and considerations (e.g. GCP, ICH, 21CFRpart11, CDISC) and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Entwicklungsingenieur für die Konstruktion (Medizintechnik)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9F4ADE49EB48E16482579F5001FC752</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Entwicklungsingenieur-f-and-amp-SHARP252r-die-Konstruktion-Medizintechnik_1641194.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Sind Sie ein Experte im Bereich der Druckmessung? Haben Sie Lust Ihr Know-how in diesem Bereich einzubringen und interessante Projekte durchzufand#252;hren? Mein Kunde aus Hamburg sucht ein Entwicklungsingenieur fand#252;r Druckmessgerand#228;te. Ihre Tand#228;tigkeiten:Sie sind hauptsand#228;chlich verantwortlich fand#252;r alle Konstruktionstand#228;tigkeiten. Auand#223;erdem unterstand#252;tzten Sie den ganzen Entwicklungsprozess von der Idee bis zum Implementierung. Des Weiteren sind Sie im Bereich der  Dokumentation und Validierung involviert.Ihr Profil:- abgeschlossenes Maschinenbau-Studium plus Vertiefung in der Druckmessung, Sensorik oder Elektrotechnik- Berufserfahrung in der Konstruktion und Entwicklung sowie gute CAD Kenntnisse sind notwendig - Erfahrung innerhalb der Medizintechnik ist von Vorteil- Sehr gute Englisch sowie Deutsch Sprachkenntnisse sowie Selbststand#228;ndigkeit und Leistungsorientierung ist gefragtHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Josand#233; Ramand#237;rez Bucheli (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Director Regulatory Affairs für ein Medical Device Unternehmen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob31E806E30F4E66F0482579F5001FC75D</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Director-Regulatory-Affairs-f-and-amp-SHARP252r-ein-Medical-Device-Unternehmen_1641195.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Global Director Regulatory Affairs fand#252;r ein Medical Device UnternehmenMein Kunde ein fand#252;hrendes Medical Device Unternehmen betreut vom Standort in Zand#252;rich aus die welweiten Zulassungsaktivitand#228;ten. Fand#252;r dieses Team von 30 Leuten suche ich aktuell einen Director Regulatory Affairs zur Leitung der Abteilung Regulatory Affairs und Postmarketsurveillance.Leben Sie wo andere Urlaub machen, Zand#252;rich ist das wichtigste wirtschaftliche, wissenschaftliche und gesellschaftliche Zentrum der Schweiz. Mehrfach schon wurde Zand#252;rich als eine Stadt mit der besten Lebensqualitand#228;t ausgezeichnet. Innerhalb kurzer Zeit sind Sie entweder im Sommer am See oder im Winter in einem der angrenzenden Skigebiete.Dies ist eine einzigartige Mand#246;glichkeit fand#252;r eine Senior Management Position. Sie sind zustand#228;ndig fand#252;r weltweite Zulassungen und Entwicklungen von Strategien zur Zulassung neuer Produkte und neuer Land#228;nder.Der ideale Kandidat hat mehrjand#228;hrige Erfahrung im Bereich Regulatory Affairs mit internationalen Zulassungen, sowie intensive Erfahrung mit dem fand#252;hren von Mitarbeitern. Deutsch und Englischkenntnisse sind zwingend erforderlich.Sie erwartet ein innovatives Unternehmen, dass in Mitarbeiter und Qualitand#228;t investiert um seine Marktposition zu erhalten und das mit attraktivem Gehaltspaket und guten Arbeitsbedingungen abrundet. Sollte Ihnen diese Position zusagen oder eine and#228;hnliche im Bereich Regulatory Affairs and#150; Medical Devices , schicken Sie mir bitte Ihre Bewerbung an c.kalous(at)real-pharma.com kontaktieren Sie mich unter +41 43 50 80 97 2.Keywords: Regulatory Affairs, RA, Zulassung, Senior Management, Line-Management, CMC, Lifecycle, Labelling, CTD, CTA, MRP, DCP, MAA, eCTD, FDA, NDA, ICH, REACH, GCP, IMPD, OTC, Christian Kalous, Kalous, Generics, Vaccines, CRO, Labeling, Pharma, Biotech, Biosimilars, Veterinary, Diagnostic, in-vitro, in vivo, FMCG, OTC, Pharma, Biotech, Medical Devicesand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager required, ZurichBasel]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD3F21C1E1267D854482579F5001FC769</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-required-Zurich-Basel_1641196.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Manager required, Zurich/BaselMein Kunde eines der fand#252;hrenden Unternehmen in der Pharmaindustrie im Bereich der Augengesundheit, hat mich beauftragt einen EU Regulatory Affairs Manager zu identifizieren.Das europand#228;ische Regulatory Affairs Team wird an diesem Standort zentralisiert und wand#228;chst zunehmend. Sie arbeiten strukturiert im Team mit einem Associate an den europand#228;ischen Zulassungen und den internationalen (LATAM/APAC) Dokumenten.Das Unternehmen dessen Name in der Industrie herausragt, ist sowohl auf den Bereich Pharma als auch Medical Devices spezialisiert. Die besten Vorraussetzungen haben Sie mit Erfahrungen in beiden Bereichen, jedoch sollten Sie als Spezialist in and#132;nurand#147; einem der beiden Bereich sich nicht von einer Bewerbung abhalten lassen.Neben interessanten globalen Aufgaben und einem attraktiven Vergand#252;tungssystem werden Sie in der Abteilung von einem Team von Regulatory Affairs Associates unterstand#252;tzt, die Sie den Fokus auf wichtige Aufgaben lenken land#228;sst. Seien Sie die Schland#252;sselfigur in den Zulassungen dieses UnternehmensIdealerweise bringen Sie ca 2 Jahre Regulatory Affairs Erfahrung im Bereich Medical Devices oder Pharma mit. Sie kennen sich mit europand#228;ischen Regularien aus, arbeiten Projekt orientiert und sprechen flieand#223;end Englisch. Fand#252;r weitere Informationen kontaktieren Sie bitte Christian Kalous bei Real Pharma unter +41 43 50 80 972 oder c.kalous(at)realstaffing.comKeywords: Regulatory Affairs, RA, Zulassung, Senior Management, Line-Management, CMC, Lifecycle, Labelling, CTD, CTA, MRP, DCP, MAA, eCTD, FDA, NDA, ICH, REACH, GCP, IMPD, OTC, Generics, Vaccines, CRO, Labeling, Pharma, Biotech, Biosimilars, Veterinary, Diagnostic, in-vitro, in vivo, FMCG, OTC, Pharma, Biotech, Medical Devices, Christian Kalousand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager für Kombinationsprodukte]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob19BA4079E4FE8F96482579F5001FC774</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-f-and-amp-SHARP252r-Kombinationsprodukte_1641197.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Manager fand#252;r KombinationsprodukteMein Kunde hat mich beauftragt einen Regulatory Affairs Manager zu identifizieren.Es handelt sich dabei um ein Biotech Unternehmen im Umkreis Zand#252;rich. Der Standort ist ideal fand#252;r Familien oder auch allein stehende. Ruhig gelegen, jedoch schnell und einfach erreichbar von Zand#252;rich, bietet der Standort Vorteile fand#252;r beide Parteien. Innerhalb von 20 Minuten erreichen Sie Zand#252;richs Innenstadt, wo Sie neben netten Einkaufsmand#246;glichkeiten und schand#246;nen Bars und Restaurants, den See fand#252;r alle mand#246;glichen Freizeit Aktivitand#228;ten finden.Das Unternehmen beschand#228;ftigt sich am Standort vollstand#228;ndig mit der Erforschung und Herstellung von Gefand#228;and#223;prothesen, sowohl mit als auch ohne Medikamenten Beschichtung.Aufgrund der erhand#246;hten Nachfrage und dem starken Wachstum wird eine Unterstand#252;tzung in der Abteilung Regulatory Affairs gesucht. In dieser spannenden Rolle sind Sie zustand#228;ndig fand#252;r die Erarbeitung von regulatorischen Angelegenheiten wand#228;hrend der Erforschung und Entwicklung neuer Produkte. Das beinhaltet sowohl europand#228;ische, als auch weltweite Neuzulassungen. Sie fungieren als Ansprechpartner fand#252;r die Zulassungsbehand#246;rden und bauen Beziehungen mit diesen auf und pflegen Sie. Es erwartet Sie eine sehr gute kollegiale Arbeitsatmosphand#228;re mit interessantem Vergand#252;tungspaket.Fand#252;r weitere Informationen kontaktieren Sie bitte Christian Kalous bei Real Pharma Zand#252;rich unter +41 43 50 80 97 2 oder c.kalous(at)realstaffing.comKeywords: Regulatory Affairs, RA, Zulassung, Senior Management, Line-Management, CMC, Lifecycle, Labelling, CTD, CTA, MRP, DCP, MAA, eCTD, FDA, NDA, ICH, REACH, GCP, IMPD, OTC, Generics, Vaccines, CRO, Labeling, Pharma, Biotech, Biosimilars, Veterinary, Christian Kalous, Christian, Kalous Diagnostic, in-vitro, in vivo, FMCG, OTC, Pharma, Biotech, Medical Devicesand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Vigilance Officer in der Nähe vom Zürichsee]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob127C58098A83DD67482579F5001FC780</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Vigilance-Officer-in-der-N-and-amp-SHARP228he-vom-Z-and-amp-SHARP252richsee_1641199.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Vigilance Officer in der Nand#228;he vom Zand#252;richseeMein Kunde ist ein Medical Device Unternehmen spezialisiert auf die Herstellung von Implantaten. In verschiedenen Feldern ist der Name marktfand#252;hrend und ein Synonym fand#252;r Qualitand#228;t und Innovationen. In dem Hauptsitz in der Schweiz wird neben der Forschung auch ein groand#223;er Teil produziert. In nur 25 Minuten befinden Sie sich von dem Standort in Zand#252;richs Stadtzentrum und dem See, haben jedoch auch die Mand#246;glichkeit land#228;ndlicher zur wohnen.In der Abteilung Regulatory Affairs suche ich einen Spezialisten zur Handhabung der Complaince. Das heiand#223;t  nach der Zulassung auftretende Nebenwirkungen zu einzelnen Produkten werden von Ihnen geprand#252;ft und an die einzelnen Behand#246;rden gemeldet. Sie sind dafand#252;r Ansprechpartner in Ihrem Team und intern in andere Abteilungen zur Behebung der unerwand#252;nschten Nebenwirkung.Fand#252;r diese Rolle qualifizieren Sie sich mit 2-4 jand#228;hriger Erfahrung in dem Bereich Medical Devices, bei nur 18 Monaten kand#246;nnen Sie sich auch schon gerne melden.Zusand#228;tzlich haben Sie groand#223;es Interesse an Regulatory Affairs und wollen sich in einem innovativen Unternehmen behaupten und aufsteigen. Ein Chirurgischer Hintergrund ist von Vorteil aber nicht Voraussetzung. In Deutsch und Englisch sind Sie allerdings sehr gut. Sollte Ihnen diese Position zusagen oder eine and#228;hnliche im Bereich Regulatory Affairs and#150; Medical Devices interessieren, schicken Sie mir bitte Ihre Bewerbung an c.kalous(at)realstaffing.com oder kontaktieren Sie mich unter +41 43 50 80 97 2.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Device RA Specialist required near Zurich]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7FAF1103B3BF0D5F482579F5001FC78C</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Device-RA-Specialist-required-near-Zurich_1641200.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Medical Device RA Specialist required near ZurichFor my client, a leading company in the field of medical devices with its headquarter near Zurich, I was asked to identify a Regulatory Affairs specialist to increase their department.The market this company is working on is increasing and delivering high potential to develop careers in. As a matter of fact the company is spending more than 5% of the gross profit into research and development to ensure their leading position on the market. Its Philosophies is to be No 1 deliverer for their Patients worldwide and to ensure this, workshops and trainings for patients and doctors are hold frequently.Regulatory Affairs plays a big role in the company, to secure their market position with new submissions and reviewing actual regulations your team will keep the pipeline up and ensure an ongoing company success.I am looking for individuals who would like to take their career forward; ideally you have already experience in regulations within medical devices. German is not a must but helpful.The company is consistently investing in their staff and building up individuals internally to develop their career into new responsibilities, this will then be round up by a good salary package with good benefits. I am a specialist Regulatory Affairs Headhunter / Recruitment consultant who is Zurich based, and I work only on roles in Switzerland. This is one example of a portfolio of over twenty positions on which I am currently working. For more information on this or other roles, contact Christian Kalous at Real Pharma Zurich on 043 50 90 97 2 or email c.kalous (at)real-pharma.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Kandidat Swiss Medic Erfahrung gesucht in Zürich]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0B49114A3884E5F8482579F5001FC7A1</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Kandidat-Swiss-Medic-Erfahrung-gesucht-in-Z-and-amp-SHARP252rich_1641201.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Kandidat mit Swiss Medic Erfahrung gesucht in Zand#252;richMein Kunde die Schweizer Niederlassung eines grand#246;and#223;eren Pharmaunternehmens ist aktuell auf der Suche nach einer Unterstand#252;tzung im Bereich Regulatory Affairs. Das internationale Headquarter befidnet sich auch in Zand#252;rich, so dass Sie ein Unternehmen mit Entwicklungspotential in auch andere Bereiche erwartet, das regelmand#228;and#223;ig in seine Mitarbeiter investiert und diese bei der persand#246;nlichen Entwicklung unterstand#252;tzt. Sie arbeiten eng mit den Schweizer Behand#246;rden zusammen und sorgen fand#252;r die vollstand#228;ndige Einreichung aller Unterlagen, sowie der Nachbearbeitung und Aktualisierung bestehender Zulassungen.Idealerweise haben Sie bereits Zulassungen mit den Schweizer Behand#246;rden durchgefand#252;hrt und kennen sich gut aus um selbststand#228;ndig die Aufgaben fand#252;r die Schweiz zu and#252;bernehmen. Deutsch beherrschen Sie flieand#223;end bzw. sehr gut in Wort und SchriftEs erwartet Sie eine interessante abwechslungsreiche Tand#228;tigkeit mit Eigenverantwortung und einem attraktiven Gehaltspaket.Fand#252;r weitere Informationen kontaktieren Sie bitte Christian Kalous bei Real Pharma unter 0041 (0) 43 50 80 97 2 oder c.kalous(at)realstaffing.com Als Personalberater bin ich spezialisiert auf die Vermittlung von Kandidaten im Bereich Regulatory Affairs, das bedeutet ich arbeite an mehreren offenen Positionen in der Schweiz mit groand#223;en sowie auch mittelstand#228;ndigen Kunden. In meinem Portfolio befinden sich aktuell Positionen vom Einstiegslevel als Associate bis hin zum Head of Regulatory Affairs. Sollte Ihnen diese Position nicht zusagen kontaktieren Sie mich fand#252;r weitere Positionen.Keywords: Regulatory Affairs, RA, Zulassung, Senior Management, Line-Management, CMC, Lifecycle, Labelling, CTD, CTA, MRP, DCP, MAA, eCTD, FDA, NDA, ICH, REACH, GCP, IMPD, OTC, Christian Kalous, Kalous, Generics, Vaccines, CRO, Labeling, Pharma, Biotech, Biosimilars, Veterinary, Diagnostic, in-vitro, in vivo, FMCG, OTC, Pharma, Biotech, Medical Devicesand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance HR Consultant  Recruiter  Near Frankfurt  5 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6AD78E4FA388375D482579F5001FC7AD</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-HR-Consultant-Recruiter-Near-Frankfurt-5-Months-_1641202.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Freelance HR Consultant / Frankfurt / 6 Months +A Global Pharmaceutical client are currently looking for a Freelance HR Consultant to help to assist their local HR Department near Frankfurt for an initial 5 months with the possibility of extension depending upon demand.The client is currently hiring a significant amount of new staff across a number of different Pharmaceutical related positions including Scientific and Sales positions due to a large increase in projects within the organisation from external customers.Your role will be helping with the search and selection of appropriate candidates from a variety of different sources, scheduling and attending interviews, dealing with external recruitment agencies and applicants within the company to provide all parties with accurate information regarding open vacancies and the organisation.Experience:-5 + years Human Resources / Recruitment experienceExperience with handling German Workerand#146;s CouncilPharmaceutical Industry / Medical Devices experience advantageousExperience with TALEO would be highly advantegousStrong Negotiation SkillsExcellent CommunicatorFluent English and GermanRATE: Negotiable (Depending Upon Experience)DURATION: 5 Months + (Extension possible)LOCATION: Near FrankfurtSTART DATE: ASAPIf you are interested in this position please contact Tim Heathcote at Real Pharma on + 49 (0) 69 264 898 400 or email t.heathcote(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global PharmaGenerics  Senior  Principle Regulatory Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob78A5ECA0C7DB4BE7482579F5001FC7BC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Pharma-Generics-and-amp-SHARP150-Senior-Principle-Regulatory-Specialist_1641203.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Global  Pharma/Generics and#150; Senior / Principle Regulatory Specialist (Generics) and#163;40-60kThis global pharma/generics company is growing and expanding their team and is looking for a senior regulatory associate- Easy commute from - South East/ Hertfordshire/ Cambridge/ London/ Uxbridge/ Watford, 30 minutes train from Kings Cross-and#163;30-60k-This role requires:and#149;Min 3/4 years experience and#149;Working knowledge of submissions, Variations and#149;To provide regulatory conformance support to siteand#146;s Quality, Product Manufacturing, Medical and other stakeholder groups.and#149;Has liaised with the MHRA dealing with European Marketsand#149;Working knowledge of eCTD will be a bonus, not essential as training will be givenand#149;To track all applicable regulatory changes and commitments to approval; ensuring implementation and all relevant personnel are informed or communicated.  and#149;To ensure change controls are managed correctly for the Regulatory Group and in compliance to approved procedures. (e.g. Spreadsheets, Databases and Trackers).This company emphasises on career progression and training and development. 12 months working for this company will be the equivalent of working for 18 months at a big pharma, due to the vast amount of exposure you will gain here.This is a great opportunity not to be missed, please send me your C.V or call me to discuss the role furtherNatalie Hopkins on 02077587311 or n.hopkins(a)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Science Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob20DEC23BF3858B66482579F5001FC7D3</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Science-Manager_1641204.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilitiesand#149;The person who fills this role will be expected to maintain and develop relationships with KOLs, participate in coordinating and conducting peer-to-peer interactions and medical presentations, and serve as a reviewer for independent research initiatives and publications. and#149;They will represent Medical Affairs at national and international meetings, congresses and symposiums. Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice and reviewing submissions and formulary applications will all be part of the role. and#149;The MSM will also be expected to work with cross-functional colleagues in sales, marketing, market research, training, health economics, clinical operations and external affairs. and#149;They will build solid and credible relationships with the medical community on the companyand#146;s behalf and cultivate key thought leaders and product advocates in the Academic and Community settings. If this role interests you please contact Orna Mc Donald on 02077587311 or email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Associate Director:£70k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob617340BF76CCFE6C482579F5001FC7DE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Associate-Director:-and-amp-SHARP16370k_1641205.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Regulatory Affairs Associate Director:and#60;/band#62; and#163;70k+ 1. Accountable for meeting timelines and for submission of quality regulatory documents.2. Provide direction to assigned programs by coordinating all aspects of Regulatory submissions. 3. Interact with the EMA and other international regulatory agencies, as necessary on a proactive, independent, and frequent basis. 4. For assigned projects, coordinate regulatory activities including life-cycle maintenance plans and submissions. 5. Interact effectively with regulatory colleagues, designated project teams and staff to give accurate and timely regulatory advice, and receive information. 6. Manage the timely preparation and submission of CTAs, Orphan Designations, PIPs and MAAs (and corresponding international registration packages), variations to these applications and responses to regulatory agency questions. 7. Work with Clinical and other development staff to facilitate rapid approval of pending applications.8. Keep up to date on relevant European and international guidelines, regulations, and other pertinent documents; interpret regulations and related guidelines.Experience:and#149; Seven or more years of professional experience in a technical or clinical discipline and at least five years in a regulatoryand#60;band#62;If you would like to hear more information on the role contact me on 07703013616 or email your details to n.hopkins(a)realstaffing.comand#60;/band#62; and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Oncology MSL SouthWest]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob75FB47ED3CF2E00C482579F5001FC7EA</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Oncology-MSL-South-West_1641206.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Liaising with internal and external stakeholders to exchange scientific data relating to the Oncology/ Haematology field-Responding to off-label requests from clinicians-Working on medical education activities at regional level-Staying up-to-date with all relevant clinical data/ publicationsIf this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Project Manager (CPMSCPM)  36 month contract]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAC5DB7C8D060B58F482579F5001FC7F7</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Project-Manager-CPM-SCPM-3-6-month-contract_1641207.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This is an exciting opportunity to project manage and lead core project team during study start up phase and facilitate teams ability to lead extended/complete project team. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director, this varied role will include;- Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services.- Monitor project schedule and scope to ensure both remain on track. Initiate and implement appropriate actions.- Accountable for budget across assigned project(s) including the control and minimizing of write-offs. Proactively identify out of scope activities and ensure necessary change orders are executed.- Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Covance and client requirements.- Present at external and/or internal meetings.- Ensure client satisfaction.- Supporting new staff in region and integrate them into the study process efficientlyEuropean experience is a must!!Please contact Oliver Cole for further details on 0207 758 7322.KEYWORDS: CPM, CLINICAL PROJECT MANAGER, SCPM, STUDY START UP, STUDY, START-UP, START UP, FIELD BASED, HOME BASED]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Serialisierungskoordinator in einem Pharmaco in Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob719970762FF8B521482579F5001FC80C</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Serialisierungskoordinator-in-einem-Pharmaco-in-Hessen_1641208.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Wenn sie bei einem international agierenden Pharmaunternehmen in Hessen arbeiten mand#246;chten, bei dem Sie gute Entwicklungsmand#246;glichkeiten haben, dann kontaktieren sie mich. Mein Kunde aus Hessen sucht einen Serialisierungskoordinator.Anforderungen:-Abgeschlossenes Studium der Biotechnologie, Verfahrenstechnik oder Informatik -Erfahrung in der Mitarbeiterfand#252;hrung und das Fand#252;hren von Projektteams-Sehr gute GMP Kenntnisse-Erfahrung mit den behand#246;rdlichen Strukturen zur Arzneimittelsicherheit-Umgang mit Institutionen zur Entwicklung internationaler Standards zur Fand#228;lschungssicherheit von Arzneimitteln-Teamorientierung, Kommunikationsstand#228;rke und Eigeninitiative-Verhandlungssicheres EnglischIhre Aufgaben:-Konzeption, Entwicklung und Implementierung neuer Technologien-Systeme zur eindeutiger Produktkodierung und Kennzeichnung entwickeln-Verhinderung von Produktverfand#228;lschungen mit Berand#252;cksichtigung int. und nat. regulatorischer Vorgaben   -Serialisierung von Systemen zum Originalitand#228;tsschutz-Entwickeln von Serialisierungsdaten-Management-Konzept -Sie berichten an die Herstellungsleitung -Vertretung des Kunden bei Internationalen ProjektenHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen an s.chaudhry(at)realstaffing.com. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Regulatory Affairs Consultant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE3C0C09E675F3890482579F5001FC818</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Contract-Regulatory-Affairs-Consultant_1641209.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My global client is a leader in research based pharmaceuticals and is looking for a Senior Regulatory Affairs Associate for a 12 month contract based in Sydney. This role is an exciting opportunity to work on a broad range of therapeutic areas from general medicines, specialty medicines, womens health and diagnostic imaging. Role responsibilities: - To ensure that all NCEs, new indications and new presentations are registered in the best possible time fram and with the best possible labels - To ensure that all company products remain compliant with all relevant regulatory and corporate requirements throughout their product lifecycle - To partner with relevant stakeholders within the company to assist in achieving optimal company outcomes - Registration of new products, indications and presentations - Maintenance of existing products - Internal stakeholder support - External stakeholder relationships Role requirements: - Tertiary qualifications in Science of Pharmacy - 4-7 years of regulatory experience, working with prescription medicines - Working knowledge of Australian and New Zealand regulatory requirements - Ability to work unsupervised with demonstrated time management skills - Project Management skills - Experience with the new TGA processes This role requires someone who is highly autonomous and can work independently and with high quality. This opportunity will offer flexible working arrangements to the successful candidate.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Manager für Hamburg in einem Pharmaunternehmen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9A897BD62882F5B9482579F5001FC824</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Manager-f-and-amp-SHARP252r-Hamburg-in-einem-Pharmaunternehmen_1641210.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein Pharmaunternehmen in Hamburg, das fand#252;r die Entwicklung von generischen Arzneimitteln tand#228;tig ist. Im Moment wird dort ein Quality Assurance Manager gesucht.Ihre Tand#228;tigkeiten:Als Quality Assurance Manager gestalten Sie die Markteinfand#252;hrungen unserer Produkte. Die eigenstand#228;ndige Fand#252;hrung von Audits inklusive CAPA und Inspektionen bei Fertigarzneimittel und Wirkstoffherstellern. Sie fand#252;hren die Selbstinspektionen und Auditierungen unserer Vertragspartner durch. Sie vertreten unsere QP nach and#167;14 AMG bei der Freigabe von Fertigarzneimittel und Wirkstoffen. Ihr Profil:- Abgeschlossenes Studium der Pharmazie, (Apotheker) am besten mit der Qualifikation als Sachkundige Person nach and#167; 15 AMG- Mehrere Jahre Erfahrung in der Qualitand#228;tskontrolle oder der Qualitand#228;tssicherheit fand#252;r Arzneimittel- Teamfand#228;higkeit- Flieand#223;ende Deutsch und Englischkenntnisse- Starke analytische und kommunikative Fand#228;higkeiten- Zielstrebig und teamorientiertHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen unter s.chaudhry(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ICT technician for contract manufacturer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7C8773240446D384482579F5001FC830</referencenumber>
<City><![CDATA[Limburg]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ICT-technician-for-contract-manufacturer_1641211.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[For one of my customers Iand#146;m looking for a (CSV) validation professional with a good knowledge of GAMP5 and 21 CFR part 11 compliance. The company is a contract manufacturer which focuses on human cell/tissue culturing for biotech/biopharmaceutical companies.As an ICT technician you will be working within the QA engineering department along 5 other people. The whole organization consists of about 60 peopleDo you know your way around GMP and are you up for a challenge setting up the entire validation processes for this company? Then this is your job!Job description:Responsible for the network qualification by writing URSand#146;s, drawing up and executing of IQ/OQ/PQ protocols and mapping out the entire CSV process through GAP analysis Preparing the change control and CAPA procedures and writing of SOPs for network/user management and helpdesk activities Preparing the organization chart to map out each persons responsibilities and activitiesDefine network structures and making network component inventoryCoordinate activities with external ICT companyMaintaining contact with clients and preparing the Intranet Secondary benefits: - A competitive salary between and#128;3800 en and#128;4600 per month- Attractive secondary benefits including pension and travel cost reimbursementRequirements:- BSc in Informatics / comparable- Profound knowledge of GMP- Minimum of two years work experience in validation (CSV)- Good knowledge of GAMP5 and 21 CFR part 11 compliance and SQL server- English: fluent, both spoken and written; Good knowledge of Dutch is nice to haveAre you enthusiastic about this vacancy and do you want to learn more? Please press the and#145;applyand#146; button and upload your cv for Gwen Reniers. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Principal Validation Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8171BBDDF7CDBE95482579F5001FC83D</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Principal-Validation-Engineer_1641212.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The Principal Validation Engineer will report directly into the Manager of Validation. This position allows for direct management of indivduals and is a major contributor to a department of quality and validation engineers. Primarily responsiblies include:-Manage and plan projects in relocation to engineering techniques, procedures.-Ability to prioritize multiple tasks.-Supervises/coordinates an engineer and/or technicians on assigned work.- Act as the SME for validation issues and specific area such as process and equipment.* Provide innovative and novel approaches for tasks within the various quality systems. * Creating and/or substantially rebuilding the various quality systems as needed. * Assessing and determining the real and practical risks to product quality, regulatory compliance, GMP compliance, and business continuity. * As required, approving, reviewing, and/or making recommendations for major changes. For each change he/she will establish or determine testing criteria, effectiveness tests, on-status release requirements, affected documentation, and state of validation.* Supporting the overall Quality Management Systems* Accomplishing Certificates of Compliance that ensure that all local SOPand#146;s are in compliance.* Performing risk management tasks (FMEA, Fault Tree Analysis, etc.)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Design Electrical Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7115878CF1AD76AE482579F5001FC849</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Design-Electrical-Engineer_1641213.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for a Senior Design Electrical Engineer to join a San Jose based medical device and pharma manufacturing company. This successful manufacturing company is looking to bring on a leading member of their full time design team.Role: As a Senior Design Electrical you will be responsible for the design and implementation of specific functional electro-mechanical infusion pump units through the complete product design cycle. Responsibilities include high speed digital design, power management, analog design and electric motor control, wired and wireless communication. This role also requires the ability to mentor junior level engineers.Requirements:B.S. in Electrical EngineeringMSEE preferred8+ years of experience in hands-on design with analog and digital circuitsLeadership capabilitiesStrong communication skills for a cross-functional roleSalary:and90-115k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Project Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD9C03DE985B72BE4482579F5001FC855</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Technical-Project-Manager_1641214.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffins client immediately requires a Technical Project Manager for a contract to hire position in Menlo Park, CA.The Technical Project Manager will work collaboratively with our internal staff and our external clients to analyze the technical specifications or data files to bring them in alignment with our print and electronic services.  Primary responsibilities for this position:and#149;Provide technical solutions for clients and sales team.and#149;Pre-sales support for Sales Managers.and#149;Provides support to the sales team and project teams by delivering precise solution designs, attending customer meetings, conference calls, and assisting in facilitating technical sales on complex solutions.and#149;Provide peer reviews of implementations, configurations, and documentation for team members.Project ScopingGather business requirements into appropriate technical specifications.Support Sales Department on new Prospect Clientand#146;s data files and applications business requirements.Meetings with the Prospect and/or clients on gathering technical information in order to fulfill the analysis process.Map data fields from the data files with customer application requirements.Communicate and schedule feasibility meetings with Department Managers whenever project requirements fall out of the standard service design.Review and analyze customer requirements to create a project plan for prospect activity or implementation plan.Assist in developing existing product specifications.Other duties as assigned.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Electro Mechanical Systems Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF52BE9B52E5BB1FE482579F5001FC860</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Electro-Mechanical-Systems-Engineer_1641215.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for a Senior Electro Mechanical Systems Engineer to join a San Jose based medical device and pharma manufacturing company. This successful manufacturing company is looking to bring on a leading member of their full time team.Role: As a Senior Electro Mechanical Systems engineer you will be responsible for the re-design and testing of sophisticated electro-mechanical systems and components as well as the generation of analytical models and test methods. Self-direction as well that the ability to lead others is important to this roles success. This roles requires the capability to analyze and develop advanced algorithms for systems involving motors, actuators and sensors.Requirements:B.S. in Mechanical Engineering12+ years of experience in mechanical engineering field(MSME with 10 years of experience may substitute for above)Proven record in design and development of electro-mechanical systemsFamiliarity with C++ and VB codes, also LABVIEW scriptsLeadership capabilitiesStrong communication skillsSalary:and90-120k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Auditor  Medical Devices  £40k  Oxford]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA74217BD3A9E3943482579F5001FC877</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Auditor-Medical-Devices-and-amp-SHARP16340k-Oxford_1641216.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This global organisation is looking for a qualified lead auditor with experience of auditing to ISO:13485.They will have had experience scheduling their own audits previously and travelling internationally to other internal sites, clients, suppliers and other internal departments. They will need to have 3+ of lead auditing experience.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Manager  Medical Devices  Surrey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB154F3E305A6AD17482579F5001FC884</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Quality-Manager-Medical-Devices-Surrey_1641217.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Join a world renowned medical device organisation that is in a period of strong growth due to a number of acquisitions. This role offers strong progression within the company and the ability to develop to Director level if you show the correct skills and drive.They are looking for a manager that has experience of interacting in the global market and has the ability to interact multisite and manager a large group in a direct and also a matrix system. This candidate will need to have experience of Class II-III devices as well as the ability to develop staff beneath them This candidate needs to have a science related degree.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pricing and Market Access Manager  Up to Circa £90,000]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6FE0D6F42D1553D3482579F5001FC89A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pricing-and-Market-Access-Manager-and-amp-SHARP150-Up-to-Circa-and-amp-SHARP16390000_1641218.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing are proud to be working along side a market leading consultancy that provide scientific and commercial expertise to the pharmaceutical and Life sciences Industry. In recent years the organisation have experienced a significant period of growth and are committed to investing back within the organisation to ensure that they continue to be recognised as one of the leading providers of data to the pharmaceutical and health care industries. A key area that the CRO are keen to develop is the Pricing and Market Access department and subsequently a position has arisen for a new Pricing and Market Access Engagement Manager.  The Engagement Manager will play a pivotal role in delivering projects and developing strategies that provide top quality support to leading pharmaceutical executives. Therefore Engagement Managers have a high level of responsibility and need to be highly committed to delivering the best possible outcomes for projects and clients.We are looking for pricing and market access professionals who are exceptional strategic and analytical thinkers who can apply this to deliver high quality projects and develop client-oriented solutions. The ideal candidate will possess  Project leadership and client relationship skills and have the ability to demonstrate excellent commercial, analytical, problem-solving, communication, interpersonal and leadership skills. On offer is a salary of up to circa and#163;90,000 depending on experience and the chance to work for a global market leading organisation. For more information please contact Immanuel Ross at Real Staffing on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Senior Clinical Research Associate Hessen  3  mon. 1.0FTE]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4B6CC72F010777D6482579F5001FC8A5</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Senior-Clinical-Research-Associate-Hessen-3-mon-10FTE_1641219.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a large Pharmaceutical Company based in Hessen who are looking for a Freelance Senior Clinical Research Associate (CRA) with experience in diverse Indications.You will be working 2 days Monitoring, 2 days Office and 1 day Home based. The SCRA must have the following Qualifications:Key Responsibilities:and#149;Preparing and supervising the clinical studies for substances in different areasand#149;Monitoring of clinical studiesand#149;Good knowledge in Ethic submission and documentationand#149;Coordinating the CRA team and also  Quality controland#149;Very good skills in GCP and clinical trialsExpertise and Complexity:and#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilityand#149;Fluent German Salary/ Duration:and#149;Start 15.05.2012and#149;End  15.08.2012 (with option on extension)Apply now! Call Parminder Singh at Real Pharma on +49 69 264 89 8400 or send your CV to p.singh(at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Leader  Manchester  Procedure Packs  £40k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob30C8ADFE4C7BE040482579F5001FC8B3</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Leader-Manchester-Procedure-Packs-and-amp-SHARP16340k_1641220.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Below are details of a role at a global medical device organisation, this position offers the candidate a great career progression within an organisation that services countries all over the world.Job Overview:Due to an internal move I am currently representing a global client for the position of Regulatory Affairs Specialist.  The role is to primarily manage the regulatory activities throughout the product life cycle that support the companies Procedure Packs.  The ideal candidate must be a regulatory affairs professional with a strong background in the medical devices industry.  Knowledge and experience of procedure packs is highly desirable.  Job Description:Execute the pre-market process in order to secure compliance and thereby achieve CE Marking Authorisation and other product approvals for medical devices.Execute the post-market process in order to secure compliance and thereby maintain CE Marking Authorisation and continuous product approvals for medical devices.Key Accountabilities:Key accountabilities include but not limited to:Responsible for managing and supervising the regulatory activities in support of both existing and new products.  This includes anticipating regulatory obstacles throughout the product lifecycle and development process.Directly and frequently communicates and interacts with all departments/ functions including Manufacturing, Contract Manufacturing, Rand#38;D, Sales and Marketing with regards to regulatory and compliance issues.Competencies:In depth knowledge of European Medical Device Regulations; knows what are the main priorities concerning quality, safety and efficacy of products.Understanding of general and broader business issues.Understands corporate culture and how individuals and the organization as a whole workQualification and Experience:Batchelorand#146;s degree in a science based subject or other appropriate curriculum.Minimum of five years experience in the medical device industry whereof at least three years in regulatory affairs.Knowledge and experience of procedure packs is highly desirable.Proven ability to apply the know-how and experience in a creative way.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Account Director]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob17DABB2BC5B746CF482579F5001FC8C0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Account-Director_1641222.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a leading Medical communications and Medical Education agency based in London. They are seeking to employ a credible Account Director to lead an arm of the business in developing their networks and client base. Duties:Strategy and operational buildingDesign and creation of E-Med Ed servicesBusiness DevelopmentBuilding and developing a team of employeesCapabilitiesEnergeticResults drivenProactiveFocusedAble to build relationshipsThis is an excellent opportunity for someone with a wealth of Pharma experience to join a growing company and progress their career.For more information about benefits and a job spec, please contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  PharmaceuticalBiotechnology  Contract  Illinois]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob51B94A72DCEDBB18482579F5001FC8CD</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Pharmaceutical-Biotechnology-Contract-Illinois_1641223.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An exciting opportunity has become available at a global Pharmaceutical and Biotechnology company in Illinois.  The company is a global leader in injectable drugs and infusion technologies committed to serving customer and patient needs carried out by its highly respected and qualified employees.  The company specializes in pharmaceuticals and medication delivery with a concentration in the development and manufacturing of products to improve the safety and efficiency of patient care. The position entails regular assessments and auditing, evaluation and approval of materials, and participation in collective projects. Additionally, the position will require consultations with management, plant and suppliers as well as the ability to communicate effectively amongst all levels.  The position will also entail the development of SOPs processes as well as mentoring and training of Quality Auditors.The position requires the following:- B.S.- 6+ years of FDA/EU/Canadian/Japanese/and or Latin American regulated industry experience- Familiarity with medical product manufacturing processes- Knowledge of CFRs and ISO standards- Problem solving skills- Effective communication skills All interested candidates please apply immediately or contact Dana Leone at 312-453-9088 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Contract Biostatistician  Madrid  12 Months]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF5098DC218689DD1482579F5001FC8D9</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Contract-Biostatistician-Madrid-12-Months-_1641224.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client requires a contract biostatistician for a 12 month assignment at their site in Madrid, Spain. As a contract biostatistician you will be working on Phase III-IV global CNS studies acting as the project biostatistician. Your role will be to provide statistical input into the trial protocol, statistical analysis plan, statistical analysis and reporting on the findings of different clinical trials. Working within a team of statisticians and statistical programmers you will be reporting to the Head of Biostatistics reporting on significant milestones and results within each trial.Experience:* 5 years + pharmaceutical industry experience as a Biostatistician* Phase III and#150; IV experience * Submission experience* Excellent knowledge of different statistical methods* Strong SAS Programming skills* Excellent written and verbal communication skills in English The project team is based in Madrid therefore ideally you will be able to work at the client`s office in Madrid for 5 days per week. However you may also be able to work at the client`s offices in the UK, France or Germany if necessary. Location: ideally in Madrid but other locations possible (UK, France, Germany)Duration: 12 months + (extension possible)Rate: NegotiableStart: June 2012If you are interested in this position please contact Vincent Klauser at Real Pharma on + 49 (0) 69 264 898 400 or email v.klauser(at)realstaffing.com for more information.As a specialist recruiter in Data Management and Biostatistics positions for Pharmaceutical clients in Germany and Austria, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Account Director  North West  £40k£50k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01F4FA45E892C24C482579F5001FC8E5</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Account-Director-North-West-and-amp-SHARP16340k-and-amp-SHARP16350k_1641225.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[As head of Medical Communication recruitment at Real Pharma I am currently recruiting on behalf of a rapidly growing communications agency, who currently work with a large variety of products and brands. The position is for an Account Director, this would involve providing proactive direction of designated client accounts, being able to champion the needs of designated clients within the agency, maximizing the full potential and profitability of designated accounts and Mentoring junior staff. As Account Director some of your key responsibilities will include:and#149; To champion the needs of the accounts for which they are responsible within the agency and maximize the full potential of these accountsand#149; Responsible for the profitability of all projects on designated accountsand#149; Responsible for working with the Director, Client Services in forecasting for designated accounts,  including accurate phasingand#149; Provide guidance and day-to-day training of Account Managers and Executives on designated accountsIf you are interested in this opportunity you must:and#149; Have a degree in a relevant subject (e.g. life science) and#149; At least three years agency or relevant client side/industry experienceand#149; Mentoring/training experience If you wish to apply for the position please send an updated CV or email to r.randles(a)realstaffing.com. The position is based in the North West and looking to pay and#163;40,000-and#163;50,000.Keywords: Account Director, Med comms, Medical Communications, Medical Education, Healthcare PR, Healthcare Advertising, Senior Account Manager]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical WriterSenior Medical Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob79D9D01DAFDC2FA0482579F5001FC8F0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Writer-Senior-Medical-Writer_1641226.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading medical communications agency is seeking to employ a medical writer to join their growing team. My client prides themselves on passion and enthusiasm to succeed with excellent career progression.The role will involve:Publication PlanningMeeting plansClient facing exposureSymposiaand#146;sManuscriptsAbstractsThis emerging medical communications agency is located in the South East and is looking to pay a competitive salary depending on experience.For more information please contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR MEDICAL WRITER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob70BE619000C82319482579F5001FC8FC</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-MEDICAL-WRITER_1641227.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[I am currently recruiting on behalf of an integrated Healthcare Communications Agency, who is seeking to expand and grow their Editorial arm by brining on board a Senior Medical Writer/Scientific Specialist to take on a leadership role in this fantastic agency. You will be working very closely with the Principle Medical Writers of the company being involved in researching, writing, pitching and strategy. You must have an eye for seeing the bigger picture within the industry or the particular therapeutic area you are working on, which will cover a range from oncology, pain relief, diabetes.  The company work across a range of orphan drugs with large pharmaceutical companies who the Directors have worked with for a number of years.They company are a very energetic, passionate, trustworthy and supportive company.You must be someone who is excited by science and enthusiastic about stepping into a leadership position. You will be heavily involved in the development of scientific documentation, branding and pitching. Being a team player is essential as well as being confident in your own initiative. Client contact and liaison will be key in this role as well as a reasonable amount of travel when needed.  The company offer an excellent salary and benefits package.(The ideal candidate will have several years Med Comms experience in the UK and a science based degree.)For more information, please do not hesitate to contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director, Quality Control]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB75CEF61FD12104482579F5001FC909</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-Quality-Control_1641228.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Director, Quality Controland#60;/band#62;and#60;/uand#62;A pharmaceutical company in the San Francisco bay area is looking for a Director, Quality Control to join their team.  The Director, Quality Control will be responsible for the organizational and programmatic elements of Quality Control, Quality Assurance and Compliance functions. This responsibility includes, but is not limited to, the effective planning and organization of personnel and workflow utilization in order to implement the timely submission, approval, validation, testing and release of products and processes in accordance with applicable internal quality system policies, procedures, and external regulations and standards that govern the products manufactured, labeled, tested, stored, promoted and/or distributed.and#60;band#62;Director, QC Requirements:and#60;/band#62;and#149;  The individual must have a minimum of a Bachelorand#146;s Degree in the Life Sciences (e.g., Chemistry, Microbiology or Biology) or Pharmacy from an accredited University, with at least 7-10 years of experience in Quality Control/Quality Assurance areas related to the pharmaceutical industry. and#149;  Expertise in the areas of cGMPand#146;s, validation and regulatory compliance is necessary.and#60;band#62;If you are interested in this position, please reply to this advertisement as soon as possible.and#60;/band#62;]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Release officer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA75C8E78B8DBA47B482579F5001FC916</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Release-officer_1641229.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een internationale farmaceutische organisatie met een lokatie in Noord-Holland is op zoek naar een Quality Release officer. Het Center of Excellence Quality is verantwoordelijk voor het aansturen van het kwaliteitsbeleid van de plant in Noord-Holland. Hierbinnen is de Quality Release afdeling verantwoordelijk voor de kwaliteitswaarborging en het vrijgeven van producten voor de markt.Functie omschrijving:- Je draagt zorg voor de compliance van de kwaliteitsprocessen. - Als Quality Release Officer ben je verantwoordelijk voor de GMP correcte afhandeling van deviaties- Het toezicht houden op de diepgang van het onderzoek en het nemen van CAPAs. - Schrijven van onderzoeksrapporten- Controleren en autoriseren van SOPs- Uitvoeren van systeem audits- Zelfstandig uitvoeren van cGMP inspecties- Review en approval van PQand#146;s- Proactief meewerken aan verbetertrajecten en cGMP Secundaire voorwaarden:- Marktconform salaris van maximaal and#128;60000 incl. vakantiegeld en eindejaarsuitkering op basis van fulltime- Aantrekkelijke secundaire als vakantiedagen en atv dagen en een goede pensioensregelingFunctie eisen:- Minimaal BSc in biologie/chemie/vergelijkbaar- Werkervaring in GMP omgeving bij voorkeur in QA functie- Nederlands en Engels: vloeiend in woord en geschrift- Kennis van Lean is een preBen je geand#239;nteresseerd en wil je meer weten over deze vacature? Druk dan op de and#145;applyand#146; button en upload je cv ter attentie van Gwen Reniers.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager (développement analytique)  Brabant Wallon]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob031D06EF1F2F2F8A482579F5001FC923</referencenumber>
<City><![CDATA[Brussels Region]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager-d-and-amp-SHARP233veloppement-analytique-Brabant-Wallon_1641230.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Nous sommes un fabricant de produits pharmaceutiques et nous avons rand#233;cemment ouvert une nouvelle unitand#233; de dand#233;veloppement. Pour soutenir notre croissance, nous sommes aujourdhui and#224; la recherche dun Chef de projet Dand#233;veloppement Analytique pour rejoindre notre and#233;quipe situand#233;e dans le Brabant wallon.Vos tand#226;ches:- Supervision dand#146;une and#233;quipe de Chimistes- Le dand#233;veloppement, lamand#233;lioration et la validation des mand#233;thodes analytiques- Rand#233;vision de la partie analytique des dossiers- Gestion de projets- Point de contact pour les clientsVotre profil:- Dipland#244;me scientifique (pharmacien, chimie, biologie ...)- Fluent en FR / EN- + / - 3 ans dexpand#233;rience au sein dun laboratoire- Une expand#233;rience avand#233;rand#233;e dans le dand#233;veloppement et la validation des mand#233;thodes analytiques- Une expand#233;rience en gestion des personnes en tant que superviseur,    coordinateur ou team leader- Une expand#233;rience avec les mand#233;thodes analytiques chimiques et biologiques- Leadership- Flexible- Excellentes qualitand#233;s relationnellesNotre offre:Un salaire attractif basand#233; de votre expand#233;rience (entre and#128; 50 000 - and#128; 55 000) + avantages.Postulez dand#232;s maintenant en envoyant votre CV and#224; jour ou contacter Claudia Nigeon au +32 (0) 2 610 59 00 pour plus dinformations. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Process Manager Drug Safety (mw) gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob18207ECC05CFF45D482579F5001FC930</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Process-Manager-Drug-Safety-m-w-gesucht_1641231.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Process Manager Drug Safety (m/w)Fand#252;r ein deutsches Pharmaunternehmen suche ich ab sofort einen and#60;band#62; Process Manager Drug Safety (m/w) and#60;/band#62;!Aufgaben:and#149;medizinische Bewertung und Bearbeitung von unerwand#252;nschten Nebenwirkungsmeldungenand#149;selbststand#228;ndige Optimierung der Pharmakovigilanz Prozesseand#149;Beantwortung von Anfragen von and#196;rzten, Apothekern und Behand#246;rdenand#149;Bearbeitung entsprechend SOPsand#149;Zuverland#228;ssige Prand#252;fung der lokalen SOPs/ WPDs und STLsFand#252;r diese Stelle sollten Sie folgende and#60;band#62; Eigenschaftenand#60;/band#62; nachweisen kand#246;nnen:and#149;Abschluss eines pharmazeutischen Studiums oder naturwissenschaftlichen Studiumsand#149;fundierte Industrieerfahrung  in der Pharmakovigilanzand#149;zuverland#228;ssige und eigenstand#228;ndige Arbeitsweiseand#149;flieand#223;end Deutsch und Englisch in Wort und SchriftGerne erhalten Sie diskret und fachlich kompetent weitere Details. Ihr Ansprechpartner ist Hanna HolowatyTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, max. 1MB, and#252;ber den Online Bewerbungslink oder an and#60;band#62; h.holowaty(at)realstaffing.com and#60;/band#62;und rufen Sie mich an.  Weiterhin besetze ich deutschlandweit weitere Positionen, als Festanstellungen, im Bereich der Pharmakovigilanz und im Medical Affairs. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete neue Perspektiven.Besuchen Sie mein XING Profil fand#252;r weitere Informationen.https://www.xing.com/profile/Hanna_Holowatyand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs CMC in MITTELHESSEN]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4A73715E668D707F482579F5001FC93B</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-CMC-in-MITTELHESSEN_1641232.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client specializes in the treatment of strong pain and supplies medicines for substitution and tumour treatment, as well as antiseptics and wound treatment. At the moment they are looking for a REGULATORY AFFAIRS MANAGER CMC. Do you want to work internationally in areas such as the EU, Asia-Pacific, and Latin America?Your responsibilities will be project management for regulatory submissions, renewals and variations. In addition to that you will be giving regulatory and scientific guidance to the project teams for all CMC related questions. Supporting internal and#38; external compliance through critical assessment of CMC documentation and GMP processes will also be part of your job spec.Do you want to work cross functionally to design, initiate and deliver on-time projects and compliance initiatives throughout the business?What you need to bring along:Scientific degree, experience in Regulatory Affairs (Preferred working  experience in areas of Rand#38;D, QC or operational pharmaceutical departments) as well as strong experience in International regulatory procedures and requirements (EU, Asia-Pacific, Latin America). Understanding of both English and German languages is a must.For further information about this great opportunity, please e-mail or call Frank Seipel (Senior Regulatory Affairs Recruitment Consultant) at Real Pharma on 0049 (0) 69 26 489 8400.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead SAS Programmer  Medical Devices  Contract  Illinois]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0707660BDCF5B693482579F5001FC947</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Lead-SAS-Programmer-Medical-Devices-Contract-Illinois_1641233.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a leading Medical Device Company based in Illinois, now has a fantastic opportunity to work on clinical trials for Class II and III Medical Devices.  This is a 6 month initial contract paying and60 - and70 per hour.My client is currently experiencing a large increase in workload due to the successful nature of a number of products that are currently in Development at the client site.  Due to the invasive nature of these products my client requires a strong Lead SAS Programmer to head up the creation of Tables, Listings and Figures in line with the Statistical Analysis Plan.  This role will also include working on CDISC.  As this is a Medical Device project the life cycle will not exactly match that of a drug development project however there are similarities to Phase II and III Clinical Trials.Candidates for this position must have the following skills and experience:- Masters Degree or higher within Computer Science or related field- 5+ years SAS programming experience within either Pharmaceutical or Medical Device Industries- Proven track record with CDISC- Strong ability to create Tables, Listings and Figures in line with SAPsApply now for immediate consideration or contact Tom Bakker on 312-453-9088. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Manager  Pharmacovigilance & Medical Information  £60k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCC3721F952D58824482579F5001FC954</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Manager-Pharmacovigilance-and-amp-SHARP38-Medical-Information-and-amp-SHARP16360k_1641234.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Medical Manager - and#163;60,000 + benefits - Broad remit and#38; Responsibility.My client is a global market leader with excellent prospects.With branded pharmaceutical products serving as a key area, there is a need to cater for the ever-increasing workload in Pharmacovigilance and#38; Medical Information.A manager is required that can look after headcount within both areas and experience of doing so is essential. You should have experience in copy approval and scientific input as well as covering a good amount of the PVG spectrum in your career to date.Organisational, Motivational and above all, excellent communication skills are essential to benefit within a constantly developing environment.Experience in generic products or the FMCG markets would prepare the successful candidate for this type of arena, where close contact with marketing professionals goes hand in hand with scientific aspects of the role.If you have 5+ years within EU Pharmacovigilance and#38; Medical Information and feel that you could thrive in this unique opportunity, please get in contact with your updated CV ASAP - Taran Jefferson - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Product Manager mw, Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0B0DB23DA64A3C4A482579F5001FC962</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Product-Manager-m-w-Medical-Devices_1641235.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global player in collecting and managing clinical data, in order to support clients to successfully launch drugs on the market. As an industry leader in cardiac safety drug and respiratory products, they are currently searching for a:Senior Product Manager This role is an exciting opportunity to develop the product line of a company, thus presenting you with a unique and international working environment.The position:and#149;Development of technical concepts and quality specifications for the productsand#149;Development, implementation and maintenance of the Corporate Identityand#149;Implementing and communicating marketing strategiesand#149;Overall business developmentand#149;Working closely with external partners to support the market position of the productYour Profile:and#149;Successful completion of a Bachelor/Master Degree in Engineering and#150; or relevant work experience in this fieldand#149;Extensive knowledge in respiratory, cardiology and#150; clinical products and/or patientsand#149;Professional experience with the implementation/managing of medical device products and the regulatory requirementsand#149;Knowledge and experience with healthcare ITand#149;Knowledge and requirements needed for clinical research studies and#150; specifically in respiratory and cardiologyand#149;Team skillsand#149;Good knowledge of business level English and#150; both verbally and writtenFor more information contact Simone Schaefer at Real Pharma Frankfurt on:  +49 (0) 69 264 89 8400 or Email: s.schaefer(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Science Liaison in Deutschland gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob957B95D7C7795268482579F5001FC970</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Science-Liaison-in-Deutschland-gesucht_1641236.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62; Medical Science Liaison in Deutschland and#60;/band#62;Ab sofort suche ich im Namen eines international geprand#228;gten, fand#252;hrenden  Biopharmazeutischen Unternehmens einenand#60;band#62; Medical Science Liaison in Deutschland and#60;/band#62;Hier erwarten Sie u.a. folgende and#60;band#62; Aufgabenand#60;/band#62;:and#60;liand#62;  Betreuung eines neuen Produktes in Deutschlandand#60;liand#62;  Interaktion auf Augenhand#246;he mit Key Opinion Leadernand#60;liand#62; ein fundiertes Netzwerk mit der medizinischen Gemeinschaft pflegen und ausbauenand#60;liand#62; Unterstand#252;tzung des Sales Teams vor Ort in medizinischen Fragestellungenand#60;liand#62; Medizinische Reprand#228;sentation des Kunden auf Konferenzen, medizinischen Meetings und auf Schulungsprogrammenand#60;liand#62; Schnittstelle Regulatory Compliance, Clinical Trails, scientific exchange und die scientific presentationsand#60;liand#62; Home OfficeFand#252;r diese Stelle bringen Sie folgende and#60;band#62; Eigenschaftenand#60;/band#62; mit:and#60;liand#62;  Abschluss eines medizinischen oder naturwissenschaftlichen Studiumsand#60;liand#62; fundierte praktische Erfahrung als Medical Science Manager oder Medical Advisor in Deutschlandand#60;liand#62;  ein Bonus ist, wenn Sie sich in der Ophthalmologie auskennenand#60;liand#62; Teamfand#228;higkeit und ein offenes Gemand#252;tand#60;liand#62; Deutsch und Englisch flieand#223;end in Wort und Schrift and#60;band#62; Erkennen Sie sich wieder? Erfahren Sie gerne diskret nand#228;here Infos. and#60;/band#62;Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Frau Hanna Holowaty wenden. and#60;band#62; Hanna Holowaty, Real Staffing Group  and#60;/band#62;and#60;band#62; Medical Affairs/ Pharmakovigilanz and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: h.holowaty(at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Science Liaison in Deutschland (mw)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob61D18F9B464224BD482579F5001FC97B</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Science-Liaison-in-Deutschland-m-w_1641237.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Pharma berand#228;t Unternehmen weltweit bei der Besetzung ihrer Positionen im Pharmabereich. Wir bieten auand#223;ergewand#246;hnliche Jobmand#246;glichkeiten fand#252;r talentierte Fachkrand#228;fte. Profitieren auch Sie von unserem qualifizierten Netzwerk und unserem Know-how.Ab sofort suche ich im Namen eines international geprand#228;gten, fand#252;hrenden  Pharmaunternehmens einenMedical Science Liaison in Deutschland!Welche Aufgaben wand#252;rden Sie erwarten?- Betreuung eines neuen Produktes in Deutschland- Interaktion auf Augenhand#246;he mit Key Opinion Leadern- ein fundiertes Netzwerk mit der medizinischen Gemeinschaft pflegen und ausbauen- Unterstand#252;tzung des Sales Teams vor Ort in medizinischen Fragestellungen- Medizinische Reprand#228;sentation des Kunden auf Konferenzen, medizinischen Meetings und auf Schulungsprogrammen- Schnittstelle Regulatory Compliance, Clinical Trails, scientific exchange und die scientific presentations- Mand#246;glichkeit von home officeWas bringen Sie hierzu mit?- Abschluss eines medizinischen oder naturwissenschaftlichen Studiums- fundierte praktische Erfahrung als Medical Science Manager oder Medical Advisor in Deutschland- Kenntnisse der FDA/ EMA Anforderungen- Teamfand#228;higkeit und ein offenes Gemand#252;t- Projektmanagement Erfahrung Sie werden dafand#252;r bei einem der fand#252;hrenden Unternehmen in einem dynamischen und enthusiastischen Umfeld bewegen. Das and#252;berdurchschnittliche Gehaltspaket ist natand#252;rlich nicht zu vernachland#228;ssigen.Falls Sie sich selbst wiedererkennen und diskret nand#228;here Details erfahren mand#246;chten, dann senden Sie Ihren Lebenslauf an  h.holowaty(at)realstaffing.com oder greifen Sie zum Telefon und kontaktieren Hanna Holowaty.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Teamleiter Entwicklungsingenieur Konstruktion]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCF60D4BA0E138507482579F5001FC988</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Teamleiter-Entwicklungsingenieur-Konstruktion_1641238.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mand#246;chten Sie bei einem der weltweit fand#252;hrenden Anbieter von Medizintechnik-Produkten arbeiten, bei dem sehr gute Entwicklungsmand#246;glichkeiten gegeben sind? Dann lesen Sie weiter... Mein Kunde aus Baden-Wand#252;rttemberg sucht einen Entwicklungsingenieur fand#252;r die Konstruktion von medizintechnischen Produkten.Anforderungen:and#149; Abgeschlossenes Studium im Maschinenbau, Mechatronik oder Konstruktionstechnikand#149; Erfahrungen in den Bereichen Konstruktion, Festigkeitslehre, Maschinenelemente oder Antriebstechnik, vorzugsweise in der Medizintechnikand#149; Erfahrung im Risikomanagement sowie in der  Dokumentation und Validierungand#149; Erfahrung in CAD (SolidWorks) sowie sehr gute Englisch- und Deutschkenntnisse. Ihre Aufgaben:and#149; Ihre Tand#228;tigkeit besteht aus Konstruktionsaktivitand#228;ten von komplexen Gerand#228;ten and#149; Sie unterstand#252;tzen den Entwicklungsprozess von der Idee bis hin zu der Serieneinfand#252;hrungand#149; Sie sind zustand#228;ndig fand#252;r die Design und Prozess Validierung  and#149; Dokumentation und Verifizierung gehand#246;ren darand#252;ber hinaus auch zu Ihren AufgabenHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Josand#233; Ramand#237;rez Bucheli (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Clinical Development for pharmaceutical company in NRW]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2AC7A036D63B5217482579F5001FC994</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Director-of-Clinical-Development-for-pharmaceutical-company-in-NRW_1641239.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[For my client, a big international pharmaceutical company based in NRW, I am currently looking for a Director of Clinical Development. Your responsibilities: - Leadership of  the clinical development team - Planning and implementation of the clinical development strategy - Cooperation with clinical, regulatory and quality department - Leading of the clinical section writing - Ensure compliance of program - To write and update the Clinical Development PlanIf you have min. 5 years experience in clinical development and are looking for new challenges within a pharmaceutical company, then I am looking forward to your application, including your CV. For questions and more information, do not hesitate to contact me:Yana ZinchukReal Staffing+49 (0)69 264 89 8400 y.zinchuk(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacien Affaires Réglementaires URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6A588F3BD59180E6482579F5001FC9A0</referencenumber>
<City><![CDATA[Ile]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacien-Affaires-R-and-amp-SHARP233glementaires-URGENT_1641240.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Dans le cadre dune mission de 10 mois (renouvelable) nous recherchons une personne disponible IMMEDIATEMENT pour un poste de Pharmacien Affaires Rand#233;glementaires. Ce poste est situand#233; dans le sud de Paris. Le laboratoire est une filiale France avec des mand#233;dicaments and#224; forte valeur ajoutand#233;e. Votre mission sera de travailler sur les nombreux enregistrements et variations pharmaceutiques de ce laboratoire.Vous and#234;tes pharmacien obligatoirement. Vous avez une expand#233;rience dau moins cinq ou six ans en Enregistrements et Variations en Affaires Rand#233;glementaires pour une filiale France. Vous maand#238;trisez langlais. Une connaissance du Contrand#244;le Publicitand#233; est un plus car cela pourrait and#234;tre une composante de la mission.Si vous souhaitez participer au dand#233;veloppement de cette entreprise, merci de transmettre votre candidature and#224; cette adresse.Je suis Antoine MUNCH de Real Pharma, cabinet de recrutement et prestations spand#233;cialisand#233; dans land#146;industrie pharmaceutique et les dispositifs mand#233;dicaux. Je travaille avec de nombreux clients ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s et des missions qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Vice President Corporate Regulatory Affairs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9AA48CE1442D0CEE482579F5001FC9AD</referencenumber>
<City><![CDATA[Rheinland]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Vice-President-Corporate-Regulatory-Affairs_1641241.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is the worlds largest fragrance company. They have a diverse product portfolio of different very famous beauty products (cosmetics, toiletries, skin care, etc.). At the moment they are looking for a new Vice President Corporate Regulatory Affairs guarantee a strong Regulatory Affairs process to support company business growth as well as to ensure compliance of regulatory requirements globally.Further you will do effective monitoring to detect emerging regulatory developments, and represent the organization at national/international associations (active membership). You will be leading a multinational team across countries (team of 7 as direct reports based in Germany), support all company brands on regulatory issues. If you a role model who talks the talk and walks the walk, donand#146;t wait and apply now. You skill set:-Scientific education, Ph.D on Pharma, Chemistry -Strong experience with worldwide Registrations-Strong leadership on international, multinational team-Fluency in English, plus good command of German   For further information about this great opportunity, please e-mail or call Frank Seipel (Senior Regulatory Affairs Recruitment Consultant) at Real Pharma on 0049 (0) 69 26 489 8400.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Toller CMC Regulatory Affairs Job in Köln]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4EF48FDB731549FD482579F5001FC9B7</referencenumber>
<City><![CDATA[Nordrhein]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Toller-CMC-Regulatory-Affairs-Job-in-K-and-amp-SHARP246ln_1641242.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein internationaler Groand#223;konzern und konzentriert sich auf Produktbereiche wie z.B. Graphics, Materials, Health Care. Als 100% Tochter, vermarktet dieses junge und schnell wachsende Unternehmen als einzigste Firma der Welt generische Kontrastmittel. Die Firma hat sich als Ziel gesetzt in diesem Nischenmarkt in den nand#228;chsten 5 Jahren Marktfand#252;hrer zu werden.Um diese Ziele zu realisieren  braucht die Firma einen Senior Manager Regulatory Affairs.Die Aufgaben:-Auf- und Ausbau des Regulatory Affairs Bereiches-Gesamtverantwortung fand#252;r den CMC-Bereich-Kommunikation mit Lohnherstellern bezand#252;glich CMC-Angelegenheiten-Projektmanagement-Regulatory Affairs-Strategy (international)-Nationale und internationale Zulassungen-Zusammenarbeit mit externen Berater-Fristgerechte Einreichungen bei den relevanten Behand#246;rden (Europa, FDA, etc.)Was sollten Sie mitbringen?-Ein abgeschlossenes Studium (Naturwissenschaften)-Internationale Regulatory Affairs-Erfahrungen-CMC-KenntnisseBei weiteren Fragen kontaktieren Sie, Frank Seipel (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Qa specialist needed middle of the Netherlands]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob46AEA3738032AF12482579F5001FC9C4</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Qa-specialist-needed-middle-of-the-Netherlands_1641243.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[At the moment I am looking for a QA specialist, highly experienced working in a (bio)pharmaceutical environment:The activities involved:-projectmanagement (multi-year management project)-coordinate the quality systems that the company works with and suggest improvements- Performing GMP related hands on activities such as CAPA, Change control, Root Cause Analysis.Candidate needs to be fluent in English and available full-time. The offered rate is around 80-90 euro per hour all-in (=also incl. travel/hotelcosts), excl VAT When interested send your CV for consideration.  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sas programmer contract, greater Boston area, year project!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob433BC1F831F8ADAE482579F5001FC9D1</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sas-programmer-contract-greater-Boston-area-year-project_1641244.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[We currently have a position open for a Clinical Programmer with between 2-7 years of experience, to join up with a large Pharmaceutical client of ours, based in The Great Boston area. The position will be to help with programming within various therapeutic areas, and is being offered as an initial 1 year contract opportunity.We are looking for local candidates with experience in the following areas:- 2-7 years experience within programming- SAS / BASAS / Excel VBA - essential- Experience with data integration projects - ETL, EAI, EII etc- Relational databases - SQL plSQL- Any experience within Data Management is a plusIf you have some experience within the relevant areas above, and are looking for a new job at the moment, then please apply by replying to this with an updated copy of your resume and one of the team will give you a call back.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Laboratory Supervisor (pharma)  Walloon Brabant]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5CBCBD60414CBCA2482579F5001FC9E1</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Laboratory-Supervisor-pharma-Walloon-Brabant_1641245.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[We are a manufacturer of pharmaceutical products and we recently open a new development unit. To sustain our growth, today we are looking for a new Laboratory Supervisor to join our team in Walloon Brabant.YOUR TASKS:- Team supervision- Development, improvement and#38; validation of analytical methods- Review of analytical parts of dossiers- Projects management - Point of contact for clientsYOUR PROFILE:- Scientific degree (pharmacist, chemistry, biologyand#133;)- Fluent in FR/EN - +/- 3 years of experience within a laboratory- Proven experience in development and#38; validation of analytical methods- Proven experience in people management (i.e: supervisor, team leaderand#133;)- Ideally experience with chemical and#38; biological methods- Leadership- Flexible- Strong interpersonal skillsOUR OFFER:An attractive salary based on your experience (between and#128;50000 - and#128;55000) + benefits Apply now by sending your updated CV or contact Claudia Nigeon on +32 (0)2 610 59 00 for more information. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Engineer  for medical device company  The Netherla]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6797F0B65D7FF5F3482579F5001FC9EE</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Engineer-and-amp-SHARP150-for-medical-device-company-and-amp-SHARP150-The-Netherla_1641246.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance Engineer and#150; for medical device company and#150; The NetherlandsAs a QA Engineer you will assist QA/RA manager with:Review operations documentation completeness and correctnessCorrect handling of rejects, deviations and non- conformities Advice for improvement of procedures, work instructions, form and Device Master RecordWe are looking for:and#149;QA Engineer with experience 1-2 years in medical device or automotive industryand#149;Experience with ISO 13485 quality systems; risk management.and#149;Nice to have: Experience/ worked according IEC 60601-1 standards Duration of the project is 5 -6months.Hourly rate: needs to be discussed. Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Project Manager  Fixed Term Contract 12 Month  Core Brands]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6E9EF2BD1ACBD521482579F5001FC9FB</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Project-Manager-Fixed-Term-Contract-12-Month-Core-Brands_1641248.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Project Manager, Marketing - Fixed Term 12 months - and#163;45K - London We are working with a leading Nutritional company who have a number of launches in the next few months and require a Fixed term contract to take a lead on all marketing activity. You will play a lead in on all launches, work cross funtionally, market research and be a major support to the Marketing team.As this role is Fixed term contract with a strong possibility of full time work and would be great experience for someone who is looking to gain more marketing experience. For further information please contact Sarra Gwilym on 0207 758 7311 or forward your CV following the details below for direct application.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager  London  Permanent]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01A9BC351DD71000482579F5001FCA05</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-London-Permanent_1641249.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regulatory Affairs Manager -Consultancy - London - Permanent My client is a global life science and outsourcing consultancy based in London. They are recruiting for a permanent Regulatory Affairs Manager with good experience in the following areas: - Supporting a team of regulatory specialists (4-5 people( - Regulatory Project Management - PSURs - Labelling - Client facing position - Matrix management This is an excellent opportunity to work with a diverse client base including Pharmaceutical, Med Devices and Biotech companies. This is a permanent position based in London on a salary of circa 55k plus benefits. Please contact Alan Lloyd on 02077587311 for more information. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CTA  Regulatory role  5 months  Brussels]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob93FD5D2EF6CC2DB9482579F5001FCA11</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CTA-Regulatory-role-and-amp-SHARP150-5-months-and-amp-SHARP150-Brussels_1641250.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is looking for a RA Manager within CTA environment for a 6 months contract. Project: and#149;Ensure effective onboarding of local Functional Service Provider (FSP) staff, including training assignment and access to their systemsand#149;Partner with other functions, including local Global Clinical Site Management (GCSM) staff, to coordinate cross functional activities and interactionsand#149;Work with FSP and their contacts to resolve questions from the FSP, key internal stakeholders, or the fieldand#149;Partner with FSP staff to ensure understanding of local regulations governing clinical research in spoke countriesand#149;Partner with FSP staff to document and maintain country-specific Clinical Trial Application (CTA) filing, safety reporting, import/export, clinical labeling, and other local requirements in appropriate systemsand#149;Initiate CTA creation process and schedule/lead regional study kick-off meetings based on receipt of signed Work Request Form(s) and#149;Ensure provision of core CTA documentation from IRR and local documentation from GCSM to spoke country FSP staff for compilation and submission and#149;Ensure all CTA filings are completed according to agreed upon submission timelinesand#149;Facilitate regulatory query resolution following established processCoordinate with FSP and GCSCM staff to ensure local customsand#146; clearance of investigational product and#149;Ensure timely regulatory review and approval of SIP packages  and#149;Ensure timely and effective maintenance of clinical trial approvals throughout the lifecycle of each clinical studyProfile:and#149;Bachelorand#146;s degree in Life Sciences, Business Administration, or a related fieldand#149;Approximately 5 years experience in biopharmaceutical/clinical researchand#149;3 years experience in Regulatory Affairsand#149;Experience in a team leadership role-Duration: 5 months-Location: Brussels-Start date: Negotiable-Rate: Market rate If interested, do not hesitate to contact Olivier Buysschaert on 02/610.59.59and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Pharma: Regulatory Affairs Executive £3035k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7F2844B3AAF42E93482579F5001FCA1E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Pharma:-Regulatory-Affairs-Executive-and-amp-SHARP16330-35k_1641251.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Salary: and#163;30-35kand#60;/band#62;This is a brilliant company offering excellent career progression, development and training.Role:- Regulatory members, develop and implement remediation plans to resolve all compliance gaps identified during the Reg Ex investigations. - This includes the required Change Control management within the Supply function to ensure effective implementation of the approved plans- Working between all product group teams within the factory, technical support and Rand#38;D- Ensure all documentation reflects current processes and meets compliance requirements- Work with factory teams to clarify perceived non conformance- Establish good communications with factory compliance and operational teamsEngineer/Science based degree or equivalent preferredYou should have: and#149; Exposure to working in a regulatory controlled environmentand#149; Understanding of manufacturing operations and have the ability to map process flowsand#149; Clearly demonstrate task and#38; time management skillsIf you are keen to find out more information on this role email n.hopkins(a)realstaffing.com or call 02077587311 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Health Economist  Global Pharma  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9260F52DFF92DA30482579F5001FCA2A</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Health-Economist-Global-Pharma-South-East_1641252.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[An exciting opportunity has arisen within a global pharmaceutical organisation that is in the process of strengthening their Market Access department by recruiting a Senior Health Economist. The Top 20 Pharmaceutical Company is one of the leading consumer medicine companies within the UK and is keen to maintain their competitive advantage by addressing the increasing challenging market access hurdles. Reporting to the Head of Health Outcomes the Senior Health Economist will be responsible for the delivery of the health outcomes strategy in the UK. The successful candidate will manage a number of high profile projects and drive the development of UK HTA submissions. The ideal candidate would hold an MSc or PhD in Health Economics and would have a proven track record of successful input in to UK HTA submissions and must be fully conversant with Health Economic Modelling and methodology. This is a fantastic opportunity for a HEOR professional keen to build on their existing skills and experience within a forward thinking market leading organisation. For further information regarding this opportunity please do not hesitate to contact Immanuel Ross at Real Staffing on 0207 758 7311]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[StatisticalSAS Programmer  £3040K  UK wide]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5F3E0ACBBE90720C482579F5001FCA3E</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Statistical-SAS-Programmer-and-amp-SHARP16330-40K-and-amp-SHARP150-UK-wide_1641253.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Statistical/SAS Programmer - and#163;30-40K and#150; UK wideI am currently recruiting for one of the biggest global CROand#146;s for the position of Statistical/SAS Programmer. The Statistical Programmer will liaise with project teams on statistical programming requirements for clinical trial projects. The statistical programmer will create tables, figures and listings utilising SAS and other analysis software.  The successful candidate will consult with the project team to create the initial system spec and design, then using SAS/GRAPH, SAS/BASE, SAS/MACRO, and SAS/STAT, they will produce tables, listing and figures for the statistical reports. They will also assist in the creation of Oracle or Oracle clinical databases.The candidate must have:and#149;A degree-level education in a biological/life-science subject or Mathematics.and#149;Statistical programming experience in either a Contract Research Organization (CRO), biotechnology, pharmaceutical or medical devices company.and#149;Clinical trial experience.and#149;Strong SAS programming skills. and#149;Experience with Oracle/Oracle Clinical databases preferable.The salary is between and#163;30-40,000 and dependant on experience. Real Pharma welcome applications from those with this experience, so please apply within or call Nelson Jordan on 02077 587311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualified Person für ein mittelständisches Pharmaunternehmen in Berlin]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobBB99063F3506FEFF482579F5001FCA4C</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualified-Person-f-and-amp-SHARP252r-ein-mittelst-and-amp-SHARP228ndisches-Pharmaunternehmen-in-Berlin_1641254.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein mittelstand#228;ndisches Pharmaunternehmen, welches eine neue Filiale in Berlin erand#246;ffnet und Zytostakia herstellt.  Im Moment wird dort eine Qualified Person and#167; 15 AMG gesucht.Ihre Tand#228;tigkeiten:Als Qualified Person sind Sie fand#252;r die Ausgabe von Chargen verantwortlich. Sie and#252;bernehmen die Verantwortung fand#252;r die Einhaltung und Zertifizierung der GMP Anforderungen. Des Weiteren sind Sie der Ansprechpartner fand#252;r die kontinuierliche Verbesserung der Qualitand#228;tssicherungsaspekte. Sie leiten Lieferantenaudits und nehmen an Kunden- und Behand#246;rdenaudits teil. Letztlich sind Sie fand#252;r die and#220;berwachung und Implementierung von CAPA zustand#228;ndig. Ihr Profil:-Abgeschlossenes Studium der Pharmazie-Mehrere Jahre Erfahrung als Qualitand#228;tssicherheitsbeauftragter in der Pharmaindustrie-Qualifizierung als Sachkundige Person nach and#167; 15 AMG (Qualified Person)-Fachwissen and#252;ber nationale und internationale relevante Regularien cGMP-Flieand#223;ende Deutsch und Englischkenntnisse-Zielstrebig und teamorientiertHabe ich Ihre Aufmerksamkeit geweckt? Dann melden Sie sich bei Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie mir direkt Ihre vollstand#228;ndigen Bewerbungsunterlagen unter s.chaudhry(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Market Access Manager  Pharma  Süddeutschland!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob74C799BBFDB4C1C7482579F5001FCA61</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Market-Access-Manager-and-amp-SHARP150-Pharma-and-amp-SHARP150-S-and-amp-SHARP252ddeutschland_1641255.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r den Bereich Market Access sucht mein Kunde ab sofort einen Senior Market Access Manager.Folgende Aufgaben erwarten Sie hier:and#149; Sie arbeiten an internationalen Projekten und Studienand#149; Sie erstellen Value Dossiersand#149; Sie arbeiten sehr eng u.a. mit den Bereichen Marketing, Medizin, und der Zulassung zusammenand#149; Sie erstellen Reports and#252;ber die aktuelle Marktsituation und machen ForecastsFand#252;r die Funktion als Senior Market Access Manager sollten Sie folgende Voraussetzungen mitbringen: and#149; Erfahrung im Bereich Market Access, Healthcare Management, Public Healthand#149; Erfahrung im Bereich evidenzbasierter Medizinand#149; Sehr gute Kenntnisse des Pharmamarktes, Rabattvertrand#228;gen, Erstattungsmodalitand#228;ten im niedergelassenen und im Klinik -  Bereichand#149; kommunikationsstarkand#149; ergebnisorientiertWer erwartet Sie als potentieller Arbeitgeber?Es erwartet Sie einer der fand#252;hrenden Global-Player, der mit seinen Mitarbeitern in and#252;ber 100 Land#228;ndern der Welt prand#228;sent ist. Der Schwerpunkt liegt auf der Forschung und damit verbunden die Entwicklung von innovativen Land#246;sungen fand#252;r die Gesundheit von Millionen Menschen.Sind Sie aktuell an solch einer Stelle interessiert? Dann bewerben Sie sich noch heute. Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produktmanager  Brand Manager  Dermatologie   Pharma  Bayern!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2238B6DF09938756482579F5001FCA70</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Produktmanager-Brand-Manager-Dermatologie-Pharma-and-amp-SHARP150-Bayern_1641256.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r die Position des Produktmanager / Brand Manager sind Sie im Bereich der Dermatologie verantwortlich fand#252;r die Planung, Durchfand#252;hrung sowie Kontrolle der Umsatz- und Absatzdaten in dem spezifischen Indikationsgebiet. Sie organisieren unter anderem Kongresse, Seminare, Fortbildungsveranstaltungen.Fand#252;r die Erstellung und Umsetzung der Marketing-Konzepte sucht mein Kunde einen Produktmanager, der ebenfalls eng mit dem Bereich Medizin zusammenarbeitet. Um der Aufgabe gerecht zu werden, sollten Sie folgendes mitbringen:and#149; naturwissenschaftlichen oder betriebswirtschaftlichen Abschluss,and#149; gute Englischkenntnisse, and#149; Erfahrungen im Pharma-Marketing sowie Pharma-Auand#223;endienst,and#149; Erfahrungen im Bereich der Dermatologieand#149; Teamfand#228;higkeit und analytisches DenkenMand#246;chten Sie in der Rolle als Produktmanager / Brand Manager im Bereich der Dermatologie bei einem Weltkonzern  beschand#228;ftigt sein? Mand#246;chten Sie auch mit Ihrer Leistung signifikant Ihren Anteil zum Firmenerfolg beitragen und mitverantwortlich sein fand#252;r die Produkte in der Dermatologie?Dann sollte das fand#252;r Sie als Produktmanager  / Brand Manager interessant sein.Wir freuen uns auf Ihre Bewerbungsunterlagen. Bei Fragen wenden Sie sich bitte an Herrn Elyas Bozan. Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Bioinformatics Contract Developer  San Francisco]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1AC37FF34F23FADC482579F5001FCA7E</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Bioinformatics-Contract-Developer-San-Francisco_1641257.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[San Francisco Synthetic Biology Company is looking for a Bioinformatics Developer to join their team.  The developer would be working on building the companys software system that is currently being used to model molecular cloning.  The ideal skillset would include:- PhD in Biology or Computer Science- Bioinformatics Coding Skills: PHP, Perl, JavaScript, MySQL- Entrepreneurial attitude - This is a small company, so a dynamic personality is key as you would be wearing many hats- Strong scientific background - having a passion for both biology and software development is key as you will be utilizing scientific knowledge on a daily basis- Familiarity working with framework Yii and GIT- Passion for participating in a project that will affect the field of medicine - Must be local to the SF Bay Area - candidates outside of this area will not be considered]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance Manager  £45k  £50k  Maidenhead]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC7556DBCB36FC44A482579F5001FCA88</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Manager-and-amp-SHARP16345k-and-amp-SHARP16350k-Maidenhead_1641258.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global top 10 pharma with excellent prospects.With the creation of a new department, a pharmacovigilance manager is needed to work autonomously at first; with a view to help increase headcount in time.Broad PVG knowledge is expected, with PSUR writing ability as a great benefit although not essential.Two years + as current team leader or manager status is sought in the potential candidate, as well as the ability to work well in a matrix type, collaborative environment.All candidates must be eligible to work in the EU.If you feel you suit the above criteria, please get in touch ASAP with your updated CV.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Market Access Director  Global Pharma  South East Eng]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob57297A16E35D10D3482579F5001FCA94</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Market-Access-Director-Global-Pharma-South-East-Eng_1641259.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A fantastic opportunity has arisen within a Global Pharmaceutical organisation for a Global Market Access Director to play an integral role within their new early phase market intelligence hub based in the UK.Committed to developing and launching innovative products, the organisation has an impressive pipeline which makes them a true market leader on a global scale. Situated in the South East of England, the successful candidate would be based in a cutting edge working environment alongside some of the very best professionals within the pharmaceutical industry.As the Global Market Access Director the main accountabilities will be to: and#149;Develop cross-functionally integrated Market Access strategyand#149;Interact with payers to build global relationships and help shape policies towards the targeted therapeutic areasand#149;Lead Value and Access Team and be accountable for reflecting payer perspective in overarching product strategySuccessful candidates would have strong communication and project management skills with a deep understanding of payer/HTA environment and evolution on a global level. Candidates must possess a strong commercial acumen and ideally 8 + years relevant experience acquired at pharmaceutical companies, HTA, physician associations or health care consultancy companies.On offer is a Salary of up to and#163;130,000 plus benefits depending on experience. For more information please contact Immanuel Ross at Real Staffing on 0207 758 7311. and#60;/uand#62;]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Scientific Engagement and Medical Affairs Advisory]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDA69F68860813536482579F5001FCAA0</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Scientific-Engagement-and-Medical-Affairs-Advisory_1641260.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The organisation is a world leading research-based pharmaceutical company with over 20000 international employees.As these are new opportunities I am recruiting for both Advisors and a Director to run the European team. Responsibilities of the Advisors include:  - Partner with the business in helping find solutions to quality and#38; compliance issues- Independently plan and conduct assessments of company studies, systems, external vendors and other Operating Companies to assure compliance with policies and procedures.- Effectively document assessment findings, and root cause analysis in an assessment report and obtain responses within established timelines.- Report and present to Medical Directors, Medical Affairs staff and Local Operating Company staff the findings of the assessment and give advice on resolving issues identified.- Maintain an up to date knowledge of appropriate national and international legislation and guidelines that affect the business.- Maintain an in depth knowledge of relevant client area processes and procedures.- Provide support as necessary to manage / report any requirements as required by regulators- Provide expertise/specialist advice on assigned areas of responsibility.- Help to educate guide and influence Rand#38;D management and staff on best quality and compliance policy and practices.- Build and maintain beneficial partnerships and working relationships with all internal and external customers.- Support inspections by regulatory authorities (local and international) relating to Scientific Engagement and Medical Affairs practices. The Director role I am recruiting for will incorporate all of the above, focussing as well on People Management and strategic planning of the future department. The Director opportunity will pay excess of and#163;90k, if you are interested in finding out more information please send me an email for a confidential discussion.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior R&D Engineer for Balloon Catheter Development]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob35D1071EB0EC551A482579F5001FCAAB</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-R-and-amp-SHARP38D-Engineer-for-Balloon-Catheter-Development_1641261.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking for a Senior Rand#38;D Engineer in the Balloon Catheter Device industry. This leading Medical Device Company is located in Fremont CA and is the leader in breakthrough treatment solutions in the medical marketplace.Company: This ground breaking medical device company is looking to bring on a full time employee with a strong engineering background, design knowledge and leadership potential.Role: As a Senior Design Engineer, you will be responsible for the full life cycle design and development of balloon catheter components, as well as related testing and analysis for product and systems. Essential skills and qualities include project planning and management, cross-functional communication between design team and board members, and ability to independently perform assignments as well as give technical guidance to lower level personnel.Requirements:B.S. in Engineering (Mechanical Engineering desirable)6+ years of engineering experience in regulated field4+ years of Medical Device experienceMust have experience with Balloon Catheter designLeadership capabilitiesStrong communication skillsSalary:and90-100k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob724F01C4AA32FD60482579F5001FCAB6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Associate-Director_1641262.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Associate Director required for a Medical Education agency just outside London.My client is a full service Medical Education Agency who are innovative, entrepreneurial and forward thinking. They are at the forefront in the industry and are looking for a passionate individual to join the team and lead the Client Services division.Responsible for:- Managing the Client Services team- Target new business whilst developing and marinating relationships with existing clients- Provide line management supervision - Provide input to the Director of Client Services, Managing Editor, and Operations Director, to ensure effective planning and efficient utilisation of account and editorial resources and skills across the Group - Provide timely and accurate budgets on all projects and ensure the Finance Manager has the necessary information for their financial planningKey skills:Background in Medical Communications in a client services roleUnderstanding of the drug development process and background in pharmaceutical medicineExcellent communication and interpersonal skillsCreativityAbility to delegate effectively and to follow up as appropriateVery good organisational skills and ability to work on own initiativeThis is a great opportunity for a Senior Account Director/Account Director to make the next step up the ladder and develop their career in an energetic, innovative agency.For more information contact rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Writer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob94993FEA3CF5560F482579F5001FCAC1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Regulatory-Writer_1641263.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is seeking to employ a Senior Regulatory Writer to join their team in South East. You will be involved in providing regulatory writing support to clients by working on projects, coaching and mentoring other staff and developing new products and services.Brief: and#149; Produce a range of regulatory documentation (including protocols, clinical trial reports, executive summaries, integrated summaries, clinical data summaries, investigator brochures, and clinical trial exemption documents). and#149; Critically review client documentation (including protocols, statistical analysis plans and tables, and listings) and#149; Accurately perform data checks on documentation produced by other members of Regulatory Writing. Requirements: and#149; Experience of writing a range of clinical documentation for regulatory authorities and#149; Writing is accurate, clear and completed within project timelines and budgets. Product or key messages are appropriately used. and#149; Can demonstrate ability to actively contribute to client / author meetings, if required, and understand their needs and requirements. and#149; Effectively monitors overall status of projects and deadlines against the project schedule. For more information, please contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Entwicklungsingenieur Mechanik (Medizintechnik)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob08648E508CD126E2482579F5001FCACD</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Entwicklungsingenieur-Mechanik-Medizintechnik_1641264.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Ein fand#252;hrendes Unternehmen in der Medizintechnik aus Hessen sucht einem Entwicklungsingenieur fand#252;r die Konstruktion medizintechnischer Gerand#228;te.Zu Ihrem Aufgabenbereich gehand#246;rt die Entwicklung und Konstruktion von mechanischer, elektromechanischer und lichttechnischer Teile und Baugruppen,  sowie die Erstellung von Dokumentationen (wie z.B. von Tests, etc.). Des Weiteren and#252;berprand#252;fen und validieren Sie fertige Medizinprodukte. Sie werden auch als Schnittstelle fand#252;r verschiedene Bereiche dienen und als Ansprechpartner fand#252;r Kunden unterwegs sein.Anforderungen: - Studium im Konstruktion, Mechatronik, Feinwerktechnik oder Medizintechnik- Erfahrung mit CAD Systemen (Pro E)- Erfahrung in der Konstruktion von Kunststoffspritzen oder Aluminiumgussteilen - Sehr Gute Englisch und Deutsch Kenntnisse Bei weiteren Fragen kontaktieren Sie, Josand#233; Ramand#237;rez Bucheli (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr. QA Specalist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3C2B59BA739320F2482579F5001FCAD7</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-QA-Specalist_1641265.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Descriptionand#149; Assist in writing change summaries and justifications to support   Document Change Orders (DCO). Review DCO documents for accuracy and compliance to procedure. and#149; Manage all Quality System documentation from creation of draft to issuance of controlled copies.and#149; Oversee the training program to comply with regulatory and internal requirements.and#149; Perform QA review of executed batch records in preparation for lot release including in-process testing, analytical release testing, and all supporting documentation.and#149; Perform raw material/component releaseand#149; Perform investigations into and document nonconformances including determination of appropriate corrective actions.and#149; Determine and/or recommend direction taken in technical product or manufacturing issues.and#149; Lead process improvements.and#149; Exercise independent judgment in quality assurance related activities.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager International Operations fuer ein Pharmaunternehmen gesucht!!!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D00D67176CF7840482579F5001FCAE3</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Manager-International-Operations-fuer-ein-Pharmaunternehmen-gesucht_1641266.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist ein mittelstand#228;ndisches Pharmaunternehmen, das sich auf die Entwicklung, Herstellung und den Vertrieb urologischer Arzneimittel spezialisiert hat. In diesem Therapiegebiet gehoert das Unternehmen zu den fuehrenden Arzneimittelherstellern in Deutschland und ist international vertreten. Ihre Aufgaben: Beratung und Betreuung der internationalen Vertragspartner sowie die Entwicklung und Erarbeitung produktbezogener Forecasts, Umsatz- und Budgetpland#228;ne sowie Produktstrategien fand#252;r die Sie zudem verantwortlich sein werden.   Sie beobachten und analysieren relevante internationale Mand#228;rkte sowie deren Zugangsbedingungen und leiten daraus Vorschland#228;ge fand#252;r Preis- und Vertriebsstrategien ab. Darand#252;ber hinaus wirken Sie mit bei der internationalen Geschand#228;ftsentwicklung sowie der Erschlieand#223;ung neuer Mand#228;rkte und sind fand#252;r die Anbahnung und Umsetzung internationaler Vertragsbeziehungen verantwortlich.Sie koordinieren alle erforderlichen Maand#223;nahmen zur Zulassung, Preisgenehmigung und Markteinfand#252;hrung von Produkten und wirken mit bei der Produktions- und Lieferplanung. Sie tragen die Umsatzverantwortung fand#252;r einzelne Land#228;nder und sind in diesen Land#228;ndern fand#252;r die Entwicklung und Umsetzung der Marketingmaand#223;nahmen direkt verantwortlich. Ihr Profil:Sie verfand#252;gen and#252;ber einen Hochschulabschluss auf naturwissenschaftlichem, betriebswirtschaftlichem oder medizinischem Gebiet und eine mehrjand#228;hrige Berufserfahrung im internationalen Pharma-Bereich. Zudem erwarten wir betriebswirtschaftliche Kenntnisse, sehr gute Kommunikationsfand#228;higkeiten und Verhandlungsgeschick. Sie verfand#252;gen and#252;ber sehr gute Englischkenntnisse und interkulturelle Kompetenzen. Analytisches Denkvermand#246;gen, konzeptionelle Fand#228;higkeiten, eine zielorientierte, strukturierte Arbeitsweise sowie unternehmerisches Denken, Verantwortungsbewusstsein und Eigeninitiative runden ihr persand#246;nliches Anforderungsprofil ab sowie das Interesse Internationales Reisen.Bei Interesse an dieser Position kand#246;nnen Sie mich gerne sowohl telefonisch als auch per E-Mail kontaktieren. Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Global Regulatory Affairs (Class II Medical Devices)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob15A2B91E77F6EBC6482579F5001FCAF9</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-of-Global-Regulatory-Affairs-Class-II-Medical-Devices_1641267.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our client is a fast growth medical device company with the need for a hands-on regulatory affairs director. With the growing regulatory department, the team is seeking someone with both domestic and international regulatory submissions/strategy experience with class II medical devices.-Generates and manages regulatory submissions for new products and changes to domestic and international health authorities (510k, CE Mark, etc.)-Responsible for regulatory strategy, guiding various teams throughout the organization (ie. marketing, Rand#38;D, quality, etc.)-Act as expert for promotional review, designs, data analysis, product labeling, etc.-Responsible for performing all duties in compliance with FDAand#146;s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Médecin Régional (MSL) VIH hf]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8E99075809123382482579F5001FCB05</referencenumber>
<City><![CDATA[Rhne]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/M-and-amp-SHARP233decin-R-and-amp-SHARP233gional-MSL-VIH-h-f_1641268.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Opportunitand#233; de carriand#232;re : rejoignez un laboratoire pharmaceutique de renom qui recherche un Mand#233;decin Rand#233;gional (MSL) VIH h/f.Votre challenge:Rattachand#233;(e) and#224; la direction des Affaires Mand#233;dicales, vous and#234;tes chargand#233;(e) de valider et diffuser la connaissance scientifique sur un portefeuille de produits en gamme virologie.Vos missions:- Dand#233;velopper un partenariat scientifique en diffusant land#146;information mand#233;dicale auprand#232;s des experts mand#233;dicaux et des autoritand#233;s de santand#233;, en accord avec la stratand#233;gie du laboratoire- Mettre en place de manifestations scientifiques en rand#233;gion (symposium, staffs), Suivi des manifestations rand#233;gionales (congrand#232;s) et rand#233;daction des comptes rendus- Contribuer and#224; la mise en place et au suivi de projets cliniques et/ou protocoles au niveau rand#233;gional (and#233;tudes acadand#233;miques, and#233;tudes observationnellesand#133;) en collaboration avec la division des Opand#233;rations Cliniques- Animer, conseiller et former les and#233;quipes dinformation mand#233;dicale et de vente- Assurer une veille sur lenvironnement mand#233;dical et juridiqueVotre profil:- Docteur en mand#233;decine ;-Idand#233;alement 3 ans dand#146;expand#233;rience dans le mand#234;me type de poste (MSL, mand#233;decin produit, mand#233;decin chef de projet clinique) au sein dand#146;un laboratoire pharmaceutique;-Trand#232;s bonnes compand#233;tences rand#233;dactionnelles et de prand#233;sentation ;-La connaissance du domaine thand#233;rapeutique est fortement apprand#233;ciand#233;eLocalisation : rand#233;gion Rhand#244;nes AlpesDate de dand#233;marrage : au plus tand#244;tEnvoyez-moi dand#232;s maintenant votre CV sous format Word!Je suis Joy Cressot, spand#233;cialisand#233;e en Affaires Mand#233;dicales au sein de Real Staffing, cabinet de recrutement basand#233; and#224; Paris. NB : Sans nouvelles de ma part dans les 3 semaines suivant rand#233;ception de votre candidature, veuillez considand#233;rer que votre candidature nand#146;aura pas and#233;tand#233; retenue pour ce poste. Je me permets toutefois de garder votre candidature pour une opportunitand#233; similaire and#233;ventuelle. Nand#146;hand#233;sitez pas and#224; transmettre cette annonce autour de vous. http://fr.realstaffing.com/fr/page/pharma_sector/]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Market Access Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob249FAEAE01FEEA92482579F5001FCB12</referencenumber>
<City><![CDATA[Gelderland]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Market-Access-Manager_1641270.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Eand#233;n van mijn klanten, een grote farmaceutische onderneming, is momenteel op zoek naar een ervaring Market Access Manager. Het gaat om een Business Unit die relatief los van het grote geheel opereert. Er is sprak van korte lijnen met het hoofdkantoor en andere affiliates in Europa en de USA. Er zijn veel bestaande producten, maar de pijplijn van nieuwe producten en subindicaties is ook groot te noemen. Verder staat er qua vergoedingen veel te veranderen, wat ook een grote impact op de markt en de organisatie gaat hebben. Men is op zoek naar iemand die overweg kan met enige wanorde. In deze functie zul je zelfstandig een deel van het portfolio runnen. Daardoor kun je hier zelf een stempel op drukken. Een netwerk in Nederland is een grote prand#233;. Concrete doorgroeimogelijkheden liggen in het verschiet.Je rapporteert in deze rol aan het Head of Market Access.* Vergoedingsstrategieand#235;n* Prijs strategieand#235;n* Gezondheidseconomische strategieand#235;n* Markt- en Concurrentie analyses* Marketing strategieand#235;n* KOL en Patient Advocacy* Budget- impact modellen Profiel:- Afgeronde WO opleiding Life Sciences, Commercieel, Business of Economisch- Minimaal 3 jaar ervaring binnen een Market Access rol- Minimaal 5 jaar ervaring binnen de Pharma - Sterke strategische marketing skills op het gebied van pricing- Resultaatgerichte instelling met team player mentaliteit- Je bent sterk communicatief vaardig, weet te sparren op verschillende niveaus- Engels, Nederlands vloeiendEen uitdagende brede functie met veel ruimte voor eigen inbreng en groeipotentie!Als je kwalificaties overeen komen met het gevraagde profiel, klik dan nu op de and#145;Applyand#146; button. Voor alle details, bel je met Egbert van Beurden op +31 20 522 1577.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Advisor Urologie]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob24A26B5D67379729482579F5001FCB1E</referencenumber>
<City><![CDATA[Brussels]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Advisor-Urologie_1641271.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mijn klant is een leidende, innovatiegedreven farmaceutische onderneming. Men ontwikkelt de allerbeste geneesmiddelen door de toepassing van de laatste onderzoeksmethoden uit wereldwijde laboratoria en van samenwerkingen met vooraanstaande wetenschappelijke organisaties. Voor het Urologie gebied zoekt men op dit moment naar een Medical Advisor. Een zeer interessante uitdaging, onder andere door een aanstaande productlancering.De cultuur van deze organisatie laat zich kenmerken door het nadrukkelijk herkennen van de specifieke talenten van haar medewerkers en het respecteren en benutten van de authenticiteit van mensen. Er heerst een no-nonsense cultuur, er wordt hard gewerkt aan een zo goed mogelijk teamresultaat. Kameraadschap en humor zijn belangrijke waarden.De Medical Advisor Urologie coand#246;rdineert zaken rondom de klinische studies en heeft een duidelijke connectie met het Brand team. Hij of zij zoekt experts om in te schakelen voor de studies en zorgt voor afstemming met internationale collegae en partners. Het werken volgens de hoogste ethische standaarden is bijzonder belangrijk in deze functie.De functie heeft veel internationale aspecten; er zal veel met Europese collegae worden samengewerkt en er zullen regelmatig congressen binnen Europa worden bezocht, wellicht ook daarbuiten. Vereisten:- Arts of MSc + PhD- Verstand hebben van klinische studies- Enkele jaren ervaring in de farmaceutische industrie. Bij voorkeur in een Medical Affairs functie, anders in een Clinical Research functie- Ervaring in Urologie is een belangrijke prand#233;, maar geen must- Perfecte beheersing van het Nederlands en Engels. Beheersing van het (gesproken) Frans is een prand#233;- Zeer vlot contacten kunnen leggen met Key Opinion Leaders- In staat zijn om complexe materie op een zeer heldere en relatief eenvoudige manier kunnen communiceren met de doelgroep- Zelfstandig en autonoom kunnen werken- Affiniteit hebben met de zakelijke doelstellingen van een farmaceutische onderneming- Team player met goede interpersoonlijke vaardigheden, netwerken kunnen bouwen- In bezit van een rijbewijs- Goed kunnen werken met MS Word, Excel, Outlook en PowerPointEen volledige functieomschrijving is op aanvraag beschikbaar.Deze werkgever biedt je zeer concurrerende arbeidsvoorwaarden, salaris maximaal and#128; 8.000 per maand. Vele extralegale voordelen, waaronder een firmawagen.Als je kwalificaties overeen komen met het gevraagde profiel, klik dan nu op de and#145;Applyand#146; button. Voor alle details, bel je met Egbert van Beurden op +31 20 522 1577.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Manager  for medical device company  The Netherlan]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7AC5D9F38A15D8F8482579F5001FCB2B</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Manager-and-amp-SHARP150-for-medical-device-company-and-amp-SHARP150-The-Netherlan_1641274.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance Manager and#150; for medical device company and#150; The NetherlandsIn this freelance position you will assist QA/RA manager with:Review Rand#38;D documentation; test reportsCoordinate risk mananagement tasksCommunicate with Notified Bodies; with external parties;.Auditing contract manufacturers and internal auditingSupport approvals of medical devices We are looking for:and#149;QA Manager with experience 5- 8years in medical device industryand#149;Experience with FDA requirements, ISO 13485 quality systems; risk management.and#149;Must have: Experience/ worked according IEC 60601-1 standards Duration of the project is 5 -6months.Hourly rate: needs to be discussed. Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Gebietsleiter für den Außendienst für ein Pharmaunternehmen gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9EFEB4C7AA13AD93482579F5001FCB38</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Gebietsleiter-f-and-amp-SHARP252r-den-Au-and-amp-SHARP223endienst-f-and-amp-SHARP252r-ein-Pharmaunternehmen-gesucht_1641276.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Unser Kunde ein Pharmaunternehmen, dass im Bereich Apotheken und Arzneimitteln angesiedelt ist sucht zum nand#228;chstmand#246;glichen Termin einen Gebietsmanager fand#252;r den Auand#223;endienst. Der Vertriebsauand#223;endienst bildet eine der wichtigsten Schnittstellen zwischen Kunden, Vertriebsinnendienst und Betrieb. Die Auand#223;endienstmitarbeiter tragen die Verantwortung fand#252;r Umsatz und Ertrag in einem fest definierten Verkaufsgebiet. Zur Verstand#228;rkung des  Vertriebsteams unseres Kunden in Sachsen (Groand#223;raum Chemnitz) suchen wir daher ab Juli 2012 eine/n Gebietsleiter/-in im Auand#223;endienst Ihre Hauptaufgabenand#149;Gewinnung von Neukunden zum kontinuierlichen Umsatzwachstumand#149;Fand#246;rderung und Unterstand#252;tzung unserer Kunden in allen vertrieblichen, kaufmand#228;nnischen und die Branche betreffenden Aufgabenstellungenand#149;Loyalisierung und Intensivierung der Geschand#228;ftsbeziehungen zu bestehenden Kunden and#149;Abschluss von umfassenden Belieferungsvereinbarungen mit Umsatz- und Ertragsverantwortungand#149;Initiierung von verkaufsfand#246;rdernden Maand#223;nahmen fand#252;r unsere Kundenand#149;Eigenstand#228;ndiges Gebietsmanagement (arbeiten als selbstand#228;ndiger Unternehmer)and#149;Einbringung neuer Ideen zur ZielerreichungIhr Profiland#149;Abgeschlossene kaufmand#228;nnische Ausbildung und erfolgreicher Abschluss eines betriebswirtschaftlichen Studium oder eine gleichwertige Qualifikation mit fundierten kaufmand#228;nnischen Kenntnissenand#149;Einschland#228;gige Berufserfahrungen im operativen Vertriebsauand#223;endienst mit nachweisbaren Erfolgen; idealerweise im Vertrieb von Dienstleistungen bzw. im (genossenschaftlichen) Handeland#149;Erfahrungen im Category-Management und in den Bereichen der Verkaufsfand#246;rderung sowie des Marketingsand#149;Kundenorientiertes Denken und Handeln, sicheres Auftreten, ausgeprand#228;gtes Verhandlungsgeschick sowie Durchsetzungsstand#228;rke und and#220;berzeugungskraft and#149;Sehr gute Fand#228;higkeit zur Selbstorganisation und hohe Eigeninitiativeand#149;Teamfand#228;higkeitLisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Specialist  Niche markt  tot 72k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1DE95AE6954E774A482579F5001FCB43</referencenumber>
<City><![CDATA[Zuid]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Specialist-Niche-markt-tot-and-amp-SHARP12872k_1641277.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Voor and#233;and#233;n van mijn klanten in de regio Rotterdam ben ik op zoek naar een Regulatory Affairs Specialist. Deze positie is beschikbaar gekomen omdat de registratie afdeling van deze organisatie gaat uitbreiden. Deze organisatie laat zich kenmerken door haar innovatieve producten binnen een niche markt. Als Regulatory Affairs Specialist ga je onderdeel uitmaken van een team van 7 personen. De Regulatory Affairs Specialist gaat zich bezighouden met het ontwikkelen en wereldwijd registreren van hun innovatieve producten. Daarnaast ben je ook het aanspreekpunt voor contract manufacturing en contract test laboratoria. Ook overleg en onderhandel je met regulatoire overheden over de registratie eisen. Dit zal zowel plaatsvinden met nationale als internationale overheden.  Functie-eisen:-Afgeronde apothekersopleiding of gelijkwaardig-3 tot 5 jaar ervaring met registraties binnen de farmaceutische / medical devices industrie-Ervaring met preklinisch en klinisch onderzoek in de farmaceutische / medical devices industrie-Process validaties (QP, OQ, IQ)-Ervaring met registratie op Nationaal, Europees, en Amerikaans niveauSalaris en oorwaarden:-Tot and#128; 72.000 bruto per jaar afhankelijk van ervaring-Goede pensioenregeling-Bonus systeem afhankelijk van persoonlijke en bedrijfsresultatenKlinkt dit als de ideale volgende stap in je carriand#232;re? Stuur dan je meest recente CV Real Staffing Group of bel 020 522 15 77 en vraag naar Robin Priems.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager Regulatory Affairs  Leidinggevende functie  tot 80k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7654136E30A576E4482579F5001FCB59</referencenumber>
<City><![CDATA[Zuid]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Manager-Regulatory-Affairs-Leidinggevende-functie-tot-80k_1641279.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Deze organisatie in Zuid-Holland is op zoek naar een Regulatory Affairs Manager. Deze positie is vrij gekomen door de groei die deze organisatie doormaakt. Deze organisatie laat zich kenmerken door haar generieke producten zoals zalven, crand#232;mes, drankjes etc. Hiervoor verzorgt deze organisatie de loonproductie voor diverse grote farmaceuten. Ook draagt deze organisatie zorg voor magistrale bereidingen en productie voor clinical trials.Als Regulatory Affairs Manager ben je eindverantwoordelijk voor de afdeling. Daarnaast stuur je 4 Regulatory Affairs Professionals aan. Ook ga je je inhoudelijk bezighouden met registraties van de producten die binnen deze onderneming worden geproduceerd. Samenstellen en indienen van registraties files zijn ook onderdeel van deze functie. Uiteraard sta je ook in contact met zowel nationale als internationale autoriteiten.  Dus heb jij:- Minimaal 2-3 jaar ervaring als RA Manager in een farmaceutische organisatie-Minimaal 3-4 jaar ervaring met samenstellen/indienen registratie files-Universitaire opleiding in Farma, Life Science of Chemie - Aantoonbare leidinggevende ervaring- Goede kennis van Nederlandse en Europese registraties - Sterke communicatieve vaardigheden, zowel mondeling als schriftelijk - Goede kennis van de Nederlandse en Engelse taal in woord en geschriftVoorwaarden:-Salaris tussen and#128;65.000- and#128;80.000 bruto per jaar-Premie vrij pensioen-Bonus and#150; afhankelijk van bedrijfs-/individuele prestatiesKlinkt dit als de ideale volgende stap in je carriand#232;re? Stuur dan je meest recente CV Real Staffing Group of bel 020 522 15 77 en vraag naar Robin Priems.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global PharmaGenerics  Senior  Principle Regulatory Officer £3055k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF5AAD542ED519F12482579F5001FCB67</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Global-Pharma-Generics-and-amp-SHARP150-Senior-Principle-Regulatory-Officer-and-amp-SHARP16330-55k_1641280.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Global  Pharma/Generics and#150; Senior / Principle Regulatory Specialist (Generics) and#163;30-55kand#60;/band#62;This global pharma/generics company is growing and expanding their team and is looking for a senior regulatory associate- Easy commute from - South East/ Hertfordshire/ Cambridge/ London/ Uxbridge/ Watford, 30 minutes train from Kings Cross-and#163;20-55kThis role requires:and#149;Min 3/4 years experience and#149;To provide regulatory conformance support to siteand#146;s Quality, Product Manufacturing, Medical and other stakeholder groups.and#149;Has liaised with the MHRA dealing with European Marketsand#149;Working knowledge of eCTD will be a bonus, not essential as training will be givenand#149;To ensure all applicable regulatory information is stored securely and that databases are maintained.and#149;To track all applicable regulatory changes and commitments to approval; ensuring implementation and all relevant personnel are informed or communicated.  and#149;To ensure change controls are managed correctly for the Regulatory Group and in compliance to approved procedures. (e.g. Spreadsheets, Databases and Trackers).This is a role where you will be working in a small team, with the opportunity to work in and learn new various tasks and procedures. This department are known for their training and development of staff. This is a great opportunity not to be missed, please send me your C.V or call me to discuss the role furtherand#60;band#62;Natalie Hopkins on 02077587311 or n.hopkins(a)realstaffing.comand#60;/band#62; and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualified Person voor farmaceutisch loonverpakker]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4D0A61879DE19FEB482579F5001FCB73</referencenumber>
<City><![CDATA[Friesland]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualified-Person-voor-farmaceutisch-loonverpakker_1641281.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Een contract manufacturer en verpakker van farmaceutische producten is op zoek naar een Qualified Person.Het bedrijf zit in het hoge noorden van Nederland en heeft Europa wijd meerdere vestigingen. In de vestiging in Nederland werken ongeveer 150 mensen van wie ruim 8 mensen op QA. Als Qualified Person zal je naast nog twee andere QPs komen te werken en rapporteer je aan de QA/RA manager Benelux. Ben jij een QP die toe is aan de volgende stap in zijn carriand#232;re en wil je in een internationale omgeving werken? Dan is dit de uitdaging voor jou!Functie omschrijving: - garanderen van de compliance met GMP zoals aangegeven in de geldende regelgeving- batches certificeren voor verkoop in overeenstemming met regelgeving- goedkeuren van de Product Quality Review, de relevante SOPs, klachten onderzoeken, deviaties- meedoen met QMS reviews, Site en Group QP vergaderingen en QP fora- eerste aanspreekpunt voor autoriteiten ten aanzien van GMP- bijdragen aan strategische en operationele initiatieven - de hele organisatie bewust maken van het leveren van kwaliteit aan klanten, zo ook patiand#235;nten door hun wensen te behartigen Secundaire voorwaarden: - marktconform salaris (op aanvraag)- reiskosten vergoeding and#128;0.19 eurocent per km- voor fulltime 192 uur vakantie- aantrekkelijke pensioensregelingFunctie eisen:- MSc Farmacie + apothekerslicentie- Geregistreerd als QP- Meerdere jaren werkervaring in de farmaceutische industrie bij voorkeur een productieomgeving- Grondige kennis van GMP/GDP- Engels: vloeiend in woord en geschrift; Nederlands is een preBen je geand#239;nteresseerd en wil je meer weten over deze vacature druk dan op de and#145;applyand#146; button en upload je cv ter attentie van Gwen Reniers.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Validation Officer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8BAC04BD7102838F482579F5001FCB89</referencenumber>
<City><![CDATA[Adelaide]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Validation-Officer_1641282.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Were seeking an experienced Validation Officer Associate to join a well known global Generic Pharmaceutical company. This contract position is for highly experienced individual with a biotechnology background, who has been primarily laboratory or production based. and#60;band#62;Reporting to the QA Manager, your main responsibilities will include:and#60;/band#62;and#149;Preparing Quality Assurance policies and procedures, particularly in relation to compliance with regulatory, statutory matters and corporate guidelines.and#149;Request and track Product Stability and Annual Product Reviews from third parties.and#149;Prepare Product Profiles.and#149;Prepare GMP contracts.and#149;Ensure compliance with government regulations, legal demands and ethical standards.and#149;Maintain appropriate records of manufacturing/packaging for future reference.and#149;Participate in and make contributions to new product launch projects.  and#60;band#62;Candidates Must Have:and#60;/band#62;and#149;Tertiary qualification in Chemistry or other life sciences.and#149;4 years experience in validationand#149;Extensive knowledge of GMP.and#149;Technical understanding of processes involved in the manufacturing, packaging, testing and stability monitoring of pharmaceutical products.and#149;Working knowledge of Quality standards and broad knowledge of Quality systems. Please notes that only successful candidates who are successful in making the shortlist will be contacted.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Trials Physician  6 months    Brussels]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA827F3B571179E80482579F5001FCB95</referencenumber>
<City><![CDATA[Flemish Brabant]]></City>
<Country><![CDATA[BELGIUM]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Trials-Physician-and-amp-SHARP150-6-months-and-amp-SHARP150-Brussels_1641283.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a biopharmaceutical company focused on the discovery and development of innovative medicines, is looking for a clinical trials physician for a contract of 6 months. Their lead product, has completed two successful Phase III clinical trials. Responsibility for all aspects of clinical study design, implementation and reporting. and#149;Provide clinical input into clinical development programmes.and#149;Lead efforts in protocol writing, all aspects of carrying out clinical trials, data analyses, writing study reportsand#149;Work with the study team ensuring the clinical aspects of protocol are carried out.and#149;Develop or approve monitoring plansand#149;Oversee feasibility assessment and investigator/site selectionand#149;Interaction with and management of CRO and other vendorsand#149;Manage and assist with Competent Authority and Ethics Committee/IRB submissionsand#149;Assist with and supporting patient recruitment tactics and processesand#149;Ensure compliance procedures and SOPs are followed.and#149;Present data to internal and external stakeholdersand#149;Be the primary contact for medical review of safety reports in pharmacovigilance.and#149;Provide clinical interpretation of safety data.and#149;Contribute to development of safety planning for studies, including Post Marketing authorisation studies and investigator sponsored studies.and#149;Contribute to the design of Risk Management plansand#149;Help with any regulatory/submission issuesand#149;Mentor Clinical Project Managers Profile: and#149;Minimum 5 years experience in Clinical Development in BioPharma industryand#149;Ophthalmology experience is an advantageand#149;Excellent organisational and time management skills, high attention to detailand#149;Strong facilitation and coordination skillsand#149;Ability to effectively prioritize and multi-taskand#149;Experience leading and managing project teams and coordinating and managing multiple projects.and#149;Personal Credibility/High ethical Standardsand#149;Thorough knowledge of the clinical trial approval processes internationally including detailed knowledge of international regulations and guidelines.and#149;Extensive knowledge of FDA, ICH and#38; GCP guidelines and regulationsProject: -Duration: 6 months with possible extensions-Location: Brussels-Start date: Negotiable-Rate: Market rate We will endeavour to respond to your application ASAP. However, there may be times when it is not possible to reply to all applications, due to high volumes of enquiries. This is sometimes the case for unsuccessful applications to one of our vacancies. We apologise for this and can reassure you that we will keep your details and contact you in the future should any suitable positions arise.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob01765AF6538EBDD0482579F5001FCBA4</referencenumber>
<City><![CDATA[Vic]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Quality-Assurance-Associate_1641284.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Were seeking an experienced Quality Assurance Associate to join a well known global Generic Pharmaceutical company. This contract position is for highly experienced quality assurance worker, looking to join a fast-paced and growing team. and#60;band#62;Reporting to the QA Manager, your main responsibilities will include:and#60;/band#62;and#149;They will be involved in product release, deviation, customer complaints and enforce the TGA and FBA stadards. and#149;Preparing Quality Assurance policies and procedures, particularly in relation to compliance with regulatory, statutory matters and corporate guidelines.and#149;Request and track Product Stability and Annual Product Reviews from third parties.and#149;Prepare Product Profiles.and#149;Prepare GMP contracts.and#149;Ensure compliance with government regulations, legal demands and ethical standards.and#149;Maintain appropriate records of manufacturing/packaging for future reference.and#149;Participate in and make contributions to new product launch projects.  and#60;band#62;Candidates Must Have:and#60;/band#62;and#149;Tertiary qualification in Chemistry or other life sciences.and#149;2-3 years experience in a QA pharmaceutical manufacturing environment.and#149;Advanced GMP knowledge.and#149;Technical understanding of processes involved in the manufacturing, packaging, testing and stability monitoring of pharmaceutical products.and#149;Working knowledge of Quality standards and broad knowledge of Quality systems. Please notes that only successful candidates who are successful in making the shortlist will be contacted.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Manager für die Pharmaindustrie im Bereich RX gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob281DF0CD22D4B7E9482579F5001FCBB0</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Manager-f-and-amp-SHARP252r-die-Pharmaindustrie-im-Bereich-RX-gesucht_1641285.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ein weltweit fand#252;hrendes Pharmaunternehmen mit 11.0000 Mitarbeitern ist in verschiedenen Bereichen unter anderem Pharma und Vision Care tand#228;tig. Zum nand#228;chstmand#246;glichen Zeitpunkt wird nun ein Product Manager gesucht, der im Bereich der verschreibungspflichtigen Medikamente angestellt werden soll. Wichtig hierbei wand#228;re, dass der Kunde auch bereit wand#228;re die Position als and#132;Juniorand#147; Stelle anzusiedeln und ebenfalls interessiert ist an Kandidaten die als Brand Manager tand#228;tig waren. Sie verfand#252;gen and#252;ber ein erfolgreich abgeschlossenes Studium der Pharmazie, Medizin, Natur- oder Wirtschaftswissenschaften? Bringen zudem mind. 2 Jahre Berufserfahrung mit ? Hiervon 1-2 Jahre im Marketing/ Produktmanagement pharmazeutischer Produkte ? Auand#223;erdem wollen Sie gerne in einem kleinen Team Ihre Fand#228;higkeiten unter Beweis stellen?Wenn Sie jetzt noch gute Englischkenntnisse sowie gute EDV Kenntnisse mitbringen, kand#246;nnte dieser Job fand#252;r Sie interessant sein!Die Aufgabe: Sie sind fand#252;r die vollstand#228;ndige Betreuung einer eigenen Produktgruppe zustand#228;ndig und entwickeln alle notwendigen Werbe, Promotion und Verkaufsfand#246;rderungsmaand#223;nahmen mit dem Schwerpunkt wissenschaftliches Marketing.Im Rahmen eines festgelegten Budgets und unter Beachtung der internationalen Marketingrichtlinien fand#252;r diese Produktgruppe sind sie fand#252;r die Erarbeitung des Marketingplans verantwortlich Die Erstellung von Produktunterlagen sowie Produktprand#228;sentationen fand#252;r die nationalen Vertriebsregionen ist ein weiterer Aspekt Ihrer Tand#228;tigkeit Sie sichern eine regelmand#228;and#223;ige Erfolgskontrolle der festgelegten Maand#223;nahmen auf der Basis von Marktbeobachtungen, Trend, Umsatz und Absatzanalysen sowie Wettbewerbsvergleichen Weiterhin arbeiten Sie eng mit dem Auand#223;endienst Durchfand#252;hrung von Schulungen und mit den anderen Marketingbereichen zusammenDie Nice to haves: Die Produktgruppe die Sie betreuen sollen sind Arzneimittel aus dem Bereich Antiinfektum and#150; idealerweise haben Sie in diesem Bereich auch schon erste Erfahrungen sammeln kand#246;nnen.Sie haben auand#223;erdem schon Erfahrungen im Bereich der Produktneueinfand#252;hrungen sammeln kand#246;nnen? Dann freue ich mich segr darauf Sie kennen zu lernen! Bei Interesse wenden Sie sich bitte an:Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Product Manager für die Pharmaindustrie im Bereich RX gesucht!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1ED4375BFCE0D1C3482579F5001FCBBD</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Product-Manager-f-and-amp-SHARP252r-die-Pharmaindustrie-im-Bereich-RX-gesucht_1641286.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ein weltweit fand#252;hrendes Pharmaunternehmen mit 11.0000 Mitarbeitern ist in verschiedenen Bereichen unter anderem Pharma und Vision Care tand#228;tig. Zum nand#228;chstmand#246;glichen Zeitpunkt wird nun ein Product Manager gesucht, der im Bereich der verschreibungspflichtigen Medikamente angestellt werden soll. Wichtig hierbei wand#228;re, dass der Kunde auch bereit wand#228;re die Position als and#132;Juniorand#147; Stelle anzusiedeln und ebenfalls interessiert ist an Kandidaten die als Brand Manager tand#228;tig waren. Sie verfand#252;gen and#252;ber ein erfolgreich abgeschlossenes Studium der Pharmazie, Medizin, Natur- oder Wirtschaftswissenschaften? Bringen zudem mind. 2 Jahre Berufserfahrung mit ? Hiervon 1-2 Jahre im Marketing/ Produktmanagement pharmazeutischer Produkte ? Auand#223;erdem wollen Sie gerne in einem kleinen Team Ihre Fand#228;higkeiten unter Beweis stellen?Wenn Sie jetzt noch gute Englischkenntnisse sowie gute EDV Kenntnisse mitbringen, kand#246;nnte dieser Job fand#252;r Sie interessant sein!Die Aufgabe: Sie sind fand#252;r die vollstand#228;ndige Betreuung einer eigenen Produktgruppe zustand#228;ndig und entwickeln alle notwendigen Werbe, Promotion und Verkaufsfand#246;rderungsmaand#223;nahmen mit dem Schwerpunkt wissenschaftliches Marketing.Im Rahmen eines festgelegten Budgets und unter Beachtung der internationalen Marketingrichtlinien fand#252;r diese Produktgruppe sind sie fand#252;r die Erarbeitung des Marketingplans verantwortlich Die Erstellung von Produktunterlagen sowie Produktprand#228;sentationen fand#252;r die nationalen Vertriebsregionen ist ein weiterer Aspekt Ihrer Tand#228;tigkeit Sie sichern eine regelmand#228;and#223;ige Erfolgskontrolle der festgelegten Maand#223;nahmen auf der Basis von Marktbeobachtungen, Trend, Umsatz und Absatzanalysen sowie Wettbewerbsvergleichen Weiterhin arbeiten Sie eng mit dem Auand#223;endienst Durchfand#252;hrung von Schulungen und mit den anderen Marketingbereichen zusammenDie Nice to haves: Die Produktgruppe die Sie betreuen sollen sind Arzneimittel aus dem Bereich Antiinfektum and#150; idealerweise haben Sie in diesem Bereich auch schon erste Erfahrungen sammeln kand#246;nnen.Sie haben auand#223;erdem schon Erfahrungen im Bereich der Produktneueinfand#252;hrungen sammeln kand#246;nnen? Dann freue ich mich segr darauf Sie kennen zu lernen! Bei Interesse wenden Sie sich bitte an:Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager Technology Transfer für Produkttransfers in Hessen]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobABB55FB091A8BB91482579F5001FCBC8</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Manager-Technology-Transfer-f-and-amp-SHARP252r-Produkttransfers-in-Hessen_1641287.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Wollen Sie fand#252;r ein weltweit agierendes Generika Unternehmen in Hessen arbeiten? Das Unternehmen exportiert seine Produkte weltweit.Im Moment wird ein Manager Technology Transfer fand#252;r Produkttransfers in Hessen gesucht.   Ihre Aufgaben:- Planung u. Durchfand#252;hrung von Produkttransfers mit Implementierungen und and#196;nderungen- Erarbeitung und Erstellung von pharmazeutischen Zulassungsunterlagen fand#252;r europand#228;ische Zulassungen and#150; Bewertung von Prand#252;f- und Herstellungsverfahren nach GMP, technologischen und analytischen Gesichtspunkten Die Anforderungen:Sie sollten ein abgeschlossenes Hochschulstudium der Pharmazie, Chemie oder Naturwissenschaften (FH, Master) haben. Des Weiteren ist  Berufserfahrung in der Pharmabranche und mit Produkttransfers erforderlich. Sie sollten Erfahrung in der Validierung, Projektmanagement, Zulassungs- und Variationsverfahren sowie Reisebereitschaft mitbringen. Es werden verhandlungssicheres Englisch vorausgesetzt.  Sollten Sie diese Vorraussetzungen mitbringen, dann haben Sie die Chance in einem stark wachsenden Unternehmen zu arbeiten. Bei weiteren Fragen kontaktieren Sie Shiraz Chaudhry (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen an s.chaudhry(at)realstaffing.com. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Manager Sr Manager of Reimbursement]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2B11F45E8C9688FE482579F5001FCBD4</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Manager-Sr-Manager-of-Reimbursement_1641288.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[This innovative medical device company specializes in the cardiovascular space. This firm has several locations however the role is located out of their west coast office.  As the Manager of Reimbursement you will be responsible for the overall strategic outlook in addition to managing relationships with payors.  In this fast paced environment you will work closely with both Medicare and key stakeholders within the industry. Reporting to the Director of Reimbursement, you will collaborate cross functionally with the clinical and marketing depts.Role:- Strong background working with clients and overalls sales experience- Broad understanding of payer schemes in hospitals/ healthcare policy- Experience working with coding and gaining coverage- Past success setting up a reimbursement hotlines- Strategize around several products in the pipeline/ gaining continued coverage Qualifications: -5-8 +years experience within strategic reimbursement at medical device or pharma Company -Strong background working with dossiers and value propositions-Expert communication and analytical skills-Thorough understanding of CMS/ Medicare and comprehensive reimbursement-Experience within pricing and contract negotiations-Bachelors from a four year university and preferred Masters in Health Policy, Health Economics, or related field, or relevant experience-Experience working with budget impact models and revenue cycle management]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6BDD415540E10B2B482579F5001FCBE1</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Regulatory-Affairs-Associate_1641290.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The Company:Our client, a global Pharmaceutical company, is looking for a Regulatory Affairs Associate. This established company is currently experiencing very strong growth over the last few quarters, due to its extensive global success. They work across pharmaceuticals, OTC Products, Devices and other areas. The Role:This exciting new role will build and maintain relationships with Regulatory and other staff within and outside the region to ensure effective communication and efficient implementation of regulatory activities. Core duties are New Product Registration, Marketed Product Maintenance / Compliance and maintaining organisational effectiveness across regional offices.The Person:The successful applicant will have at least one year Regulatory Affairs experience within the Australian or New Zealand Pharmaceutical or Medical Devices industry. They will have extensive regulatory affairs experience and have built strong working relationships with the TGA or Medsafe. If you have the drive and ambition to succeed as well as excellent communication skills combined with relevant industry experience then this could be the right opportunity for you!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Control Officer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF9ED29AA8424D5DD482579F5001FCBED</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Quality-Control-Officer_1641291.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our reputable client currently seeks a quality assurance officer to join their  Clinical Chemistry department. Applicants must be experienced and highly motivated for this senior role. You will have the opportunity to train people state-wide at any of  their 25 sites! You must be able to work in a team based environment. and#60;band#62;The Quality Control Officer will be responsible for:and#60;/band#62;1.SETUP / administration of companies DATABASE2. Training Senior Staff on higher functions 3. ENSURing THAT the regional CHEMISTRY LABORATORIES FOLLOW A UNIFORM SET OF QC RULES4.ENSURing THAT A DATABASE DOCUMENTING UNCERTAINTY OF MEASUREMENT VALUES FOR all CHEMISTRY LABORATORIES IS MAINTAINEDOVERSEEING DAILY and MONTHLY iQC reviews6.REVIEW of various manuals7.LIAISON WITH QC OFFICER RESPONSIBLE FOR EQA 8.LIAISON WITH DIAGNOSTIC COMPANIES REGARDING QC ISSUES 9. STORAGE OF SERVICE RECORDS10.management of INTraLAB QAP scheme11.Maintaining appropriate levels of data security12on-site Regional laboratory Quality control audits  and#60;band#62;Requirements of this position:and#60;/band#62;Suitable tertiary qualifications in Science or a related discipline essentialExperience in an high volume automated laboratorySuperior written and verbal communication skills. A high degree of computer skillsA working knowledge of statisticsA sound understanding of internal quality control processes, including not limited to westgard rules, sigma metrics, OpSpecs charts, Biological variation and#38; RCPA]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Research Associate]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC329095A07C319DB482579F5001FCBFC</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Clinical-Research-Associate_1641292.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you looking for a career that challenges you as an individual, but also has a positive impact? My client is a global leader in research-based drug development and is looking for a CRA to join their team. This company offers an exicting work environment, as well as exponential career opportunities. The role would be ideal for an individual who is looking to consolidate their monitoring experience whilst gaining cross-functional and mulitcultural experience across a range of therapeutic areas. This is an initial 12 month contract with a view to extend.Role responsibilities:- site management from intiation to close- budgeting and reporting on the site- management of various therapeutic areas- running patient enrolments- liaising with global counterparts and team members, as well as interactions with cross-functional teams- investigator and staff training- reporting to senior stakeholders- ensuring adherence to protocol and regulations- 50% travel within AustraliaRole requirements:- 2+ years of clinical monitoring experience within an academic, CRO or pharmaceutical environment preferred- tertiary level qualifications in a related science or health care discipline- excellent knowledge of ICH-GCP, regulatory and protocol requirements- excellent communication and organisational skills- strong monitoring abilityIf this role is of interest, please APPLY NOW or contact Gemma Macpherson on 02 8251 1100 for a confidential discussion.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Health Economist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC2DF7F5DE4C59A83482579F5001FCC07</referencenumber>
<City><![CDATA[Sydney]]></City>
<Country><![CDATA[AUSTRALIA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineeringjobs.net.au/job/Health-Economist_1641293.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, one of the worlds largest Pharmaceutical companies, is searching for a Health Economist to join their cross-functional team. This role is a once in a lifetime opportunity for a driven and passionate Health Economist where you will gain end to end experience in one of the best global companies. Role Accountabilities:- The role will have responsibility across PBAC submissions and have full end to end ownership, consequently dealing with all areas of the submission- Early development and understading clinical trials and how these will fit into the Australian Market- Cross-functional and cross-therapeutic area involvement- Providing strategic direction or input into the strategy, management and preparation of PBAC submissions To be considered for this role you must have:- A Masters in Public Health, health related PhD, post graduate qualification in Clinical Epidemiology or Biostatistics, alternatively a tertiary degree in Pharmacy, Economics, Medicine or Health Sciences; - Experience in pharmaco-economics or health economics within the Australian, Canadian or UK pharmaceutical industry, or with a large evidence based related health care sector (Government or academia), or in consulting; - PBAC submissions experience across the whole process- Excellent communication (including presentations) and writing skills If you are ready for a role that gives you ownership then APPLY NOW!]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Vertriebsmitarbeiter Plastische Chirurgie Norddeutschland]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob11F8310563A1EFA0482579F5001FCC14</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Vertriebsmitarbeiter-Plastische-Chirurgie-Norddeutschland_1641294.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Art der Tand#228;tigkeit: PermGehalt: and#128; 60.000Ort: Hamburg, NorddeutschlandMein Kunde ist ein weltweit tand#228;tiger Pharmazie- und Konsumgand#252;terhersteller. Zum nand#228;chst mand#246;glichen Zeitpunkt wird ein motivierter Vertriebsmitarbeiter (Norddeutschland), der den bestand#228;ndigen Wachstumspfad des Unternehmens weiter fortfand#252;hrt, gesucht.Ihre Hauptaufgabe liegt im Vertrieb der gut eingefand#252;hrten Medizinprodukte im Bereich Plastisch and#196;sthetischen Chirurgie. Idealerweise erfand#252;llen Sie als interessierter Kandidat folgende Kriterien:-Mindestens 3 Jahre Vertriebserfahrung, insbesondere in der plastischen Chirurgie alternativ auch bei Zahnimplantaten -Offene und kommunikative Persand#246;nlichkeit -Ehrgeizige und zielorientierte  ArbeitsweiseDes Weiteren zeichnen sich durch hohes Engagement, tadelloses Erscheinungsbild und ein zuvorkommendes Verhalten gegenand#252;ber den Kunden aus?Fand#252;hlen Sie sich angesprochen und sind Sie bereit fand#252;r eine aufregende Tand#228;tigkeit?Dann bewerben Sie sich umgehend. Fand#252;r weitere fragen steht Ihnen sehr gerne Herr and#214;ztand#252;rk zur Verfand#252;gung.Atilgan and#214;ztand#252;rk, Real Staffing GroupMedical DevicesTel.: 0049(0)69264898400E-Mail: a.oeztuerk(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Brand Manager Contract Surrey]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob020B856E463320F6482579F5001FCC21</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Brand-Manager-Contract-Surrey_1641295.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Position purposeProvide operational support to the CBLs in the implementation of brand tactics;and#149;Support customer operation excellence at country level and bring customer insight into BU to influence/shape Brand/Customer European Strategyand#149;Support the implementation/roll-out of POA at country level. Organizational relationshipsand#149;Reports to Lyrica Brand Directorand#149;Has strong relationships with all relevant internal stakeholders in country (e.g. sales management, medical function, access, finance, legal,and#133;) and above country (e.g. BTL, regional Customer and e-marketers).  Resource managedand#149;Expenses relevant to the projects for which they have responsibility. Primary dutiesand#149;Support execution of tactical plan / POA in country - lead implementation of key brand programs as directedand#149;Accountable for the planning, spending and#38; controlling of budgets agreed for own areas of responsibility, working with CBL colleagues to support regular forecast updates to aid financial planning and#149;Support product training and#149;Coordination with customer facing medical, local customer marketing and local e-marketing  colleagues for customer/digital activities/programs.Maximize revenues and#149; Completer/Finisher to drive POA implementation and#149; Business acumen and#149; Thorough understanding of revenue drivers for the brand in local country The manager is keen to interview next week. Please call Moushmi Patel on 0207 758 7322 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Entwickler Oberbayern 60.000 EUR]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA31C8ADA38098C16482579F5001FCC2E</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Entwickler-Oberbayern-60000-EUR_1641296.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde sucht ab sofort einen Software Entwickler. Das Unternehmen befindet sich in Oberbayern und hat einer seiner Geschand#228;ftsfelder in der Medizintechnik.Sie zeichnet eine hohe selbstand#228;ndige Arbeitsweise wieder? Sie sind sehr kommunikationsstark? Software Entwickler C++ and#38; C#Aufgaben:Ihre Aufgaben liegen in der Entwicklung und Realisierung von Algorithmen C++. Sie werden bereichsand#252;bergreifend eingesetzt, wie Elektronik und Optik. Sie dokumentieren alle Entwicklungsschritte und fand#252;hren Tests durch. Sie entwickeln Windows Applikationen C++ and#38; C# zur Steuerung der vorhandenen Systeme.Profil:Studium der Informatik, Elektrotechnik o.and#228;. Fundierte Erfahrung in C#, C++Gute DeutschkenntnisseBereitschaft Themenand#252;bergreifend arbeiten zu wollen.Medizintechnikerfahrung von VorteilIhnen erwarten als Software Entwickler C++ and#38; C# flexible Einsatzmand#246;glichkeiten und die Mand#246;glichkeit sich persand#246;nlich weiterzubilden. bewerben Sie sich jetzt als Software Entwickler C++ and#38; C#.Schicken Sie mir umgehend Ihr CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Technical Lead Quality Engineer for Medical Device NPD]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob62E690A4E0103C37482579F5001FCC39</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Technical-Lead-Quality-Engineer-for-Medical-Device-NPD_1641297.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is looking to fill a management role in the quality engineering field. This SF South Bay based Medical Device Company is looking for a design engineer with a quality mindset to head a team focused on new product development.Company: This rapidly growing medical device company is looking to bring on a full time employee with strong leadership capabilities.Role: As a Technical Lead Quality Engineer, you are responsible for the quality standards of a new product in its development phase. This position will work closely with the design team to test the functionality and reliability for all electrical components of the new product. Requirements:B.S. in Engineering (advanced field)Strong fundamentals in engineering of electrical componentsExperience in design for qualityQuality Assurance backgroundMinimum of 5 years of Medical Device experienceEmphasis in Medical Device Quality AssuranceLeadership capabilitiesStrong communication skillsSalary:and95-115k depending on experienceYou: If you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Market Access Consultant for international Consultancy needed]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob276A37C3C69472CE482579F5001FCC44</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Market-Access-Consultant-for-international-Consultancy-needed_1641298.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The company is a specialized strategy consulting firm with a focus on pan European market focus. They are providing deep expertise in the area of commercial strategy, operations and organizational effectiveness for the healthcare industry. For this company I am currently searching for a Business Analyst. Your day to day responsibilities will include, but are not limited to, + Reviewing and analysing of the client requirements or problems to deliver cost-   effective solutions+ High quality primary and secondary research + Support the project team in developing and communication analyses to clients+ Support specific business initiativesWorking for this international consulting company means that you will be working closely together with a team of high qualified analysts. Furthermore the company is offering you an international working place and projects at the biggest healthcare companies worldwide. Additionally the company is providing you with different internal and external trainings as well as mentoring programs to move your career even further. The working place is located in Zurich, which is offering you one of the highest living standards worldwide. I am a recruitment consultant working only in Switzerland, and specialise in HEOR and Biometrics. If you want to get further information regarding this position, or on many more like it, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com Keywords: HEOR, Health Economics and Outcomes Research, consultancy, consultant, Analyst, growing, successful, mountains, Business Analyst, Analyst, international, Top 10 pharmaco, supporting, market research, Marktforschung, Switzerland, Suisse, Schweiz, Zurich, Basel, Bern, Geneva, Genf, Geneve, Zug, Zand#252;rich, Frankreich, Deutschland, France, Germany, Skiand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Statistiker mit GMP Erfahrung gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF459705ABEAE07EB482579F5001FCC4F</referencenumber>
<City><![CDATA[Berne]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Statistiker-mit-GMP-Erfahrung-gesucht_1641299.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r eine Statistiker Position bei einem meiner Kunden in der Deutschsprachigen Schweiz suche ich zum nand#228;chst mand#246;glichen Zeitpunkt einen Statistiker bevorzugt mit GMP Erfahrung. Mein Kunde, ein international tand#228;tiges, biopharmazeutisches Unternehmen, sucht zum nand#228;chstmand#246;glichen Zeitpunkt einen Biostatistiker, der vor allem den Qualitand#228;tsbereich des Unternehmens unterstand#252;tzen soll. Das Unternehmen sieht sich aktuell in einer sehr guten Lage und mand#246;chte nun einen Statistiker haben, der das Unternehmen, vor allem die Qualitand#228;tsabteilung, unterstand#252;tzen soll. Diese Position wird komplett neu geschaffen, das heisst, dass das Unternehmen Ihnen einen sehr gute Chance bieten kann zum einen Ihre bereits gewonnenen Erfahrungen gut einbringen zu kand#246;nnen und zum anderen sehr viele neue Erfahrungen sammeln kand#246;nnen. Weiterhin bietet Ihnen diese Position die Mand#246;glichkeit die Karriereleiter sehr schnell weiter hochzuklettern. Als Biostatistiker in diesem Unternehmen unterstand#252;tzen Sie die Qualitand#228;ts- als auch die anderen Abteilungen bei relevanten statistischen Fragestellungen, prand#228;sentieren das Unternehmen gegenand#252;ber der FDA, EMEA und ICH bei statistischen Fragestellungen und sind verantwortlich fand#252;r sand#228;mtliche statistische Aktivitand#228;ten. Neben diesen Aufgaben gehand#246;rt auch die Schulung der internen Mitarbeiter mit zu Ihren tagtand#228;glichen Aufgaben.  Ich suche eine aufgeschlossene und engagierte Persand#246;nlichkeit, mit einem Universitand#228;tsabschluss in Statistik oder Mathematik. Weiterhin wand#228;ren Erfahrungen in der pharmazeutischen Industrie sowie GMP Kenntnisse von Vorteil. Sollten ich Ihr Interesse geweckt haben und Sie dann auch noch ein Teamplayer sein, der auch sehr gut Kommunizieren kann, in Deutsch und Englisch, dann freue ich mich auf Ihre aktuellen Unterlagen. Ich arbeite als Recruitment Consultant fand#252;r Real Pharma und bin fand#252;r den Bereich CDM (Clinical Data Management), SAS Programmierung und Statistik innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 435080972 zu erreichen. Keywords: SAS, STATA, Matlab, R, Schweiz, Switzerland, German, English, Deutsch, Englisch, biopharma, biopharmazeutisches Unternehmen, Bern, Berne, Biostat, Biostatistik, Biostatistician, Statistician, International, MSc, PhD, Klinische Forschung, clinical study, klinische Studie, FDA, EMEA, ICH, GMPand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Elektronik Hardware Designer Mittelfranken bis 65.000 EUR]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7883108E9900293B482579F5001FCC5A</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Elektronik-Hardware-Designer-Mittelfranken-bis-65000-EUR_1641301.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Mandant, der in Mittelfranken beheimatet ist und sein Kerngeschand#228;ft in der Medizintechnik besitzt sucht eine Elektronik Hardware Designer.Das Unternehmen operiert Welt Weit und benand#246;tigt schnellstmand#246;glich Verstand#228;rkung. Sie sind fand#252;r die Entwicklung medizinischer Systeme verantwortlich.Elektronik Hardware DesignerProfil:Studium der Elektrotechnik, technischen Informatik o.and#228;.Sie sollten bereits mehrjand#228;hrige Erfahrung in der Schaltungsentwicklung besitzen.Bevorzugt analoge Schaltungsentwicklung. Mehrjand#228;hrige Erfahrung in PCB-Layout sollte vorhanden sein. Projekterfahrungen wand#228;ren vorteilhaft.Aufgaben:Sie sind fand#252;r den gesamten Produktlebenszyklus verantwortlich. Sie entwickeln bestehende Produkte weiter. Sie sind fand#252;r die analoge Schaltungsentwicklung und PCB-Layouts verantwortlich. Sie arbeiten mit internationalen Partnern and#38; Entwicklern zusammen. Sie dokumentieren alle relevanten Entwicklungen als Elektronik Hardware Designer. Sie wollten schon immer international tand#228;tig sein? Sie mand#246;chten anhand ihrer  gewonnenen Expertise etwas fand#252;r die Menschheit tun?Dann bewerben Sie sich jetzt als Elektronik Hardware Designer.Senden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Consultant im Bereich Projekt Management gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5A98FB1EF1010C74482579F5001FCC67</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Consultant-im-Bereich-Projekt-Management-gesucht_1641302.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Das Beratungshaus ist auf den Bereich Informations- und Qualitand#228;tsmanagement als auch auf IT Management spezialisiert und betreut in diesem Bereich verschiedenste Unternehmen der Life Science Branche. Fand#252;r ein Mittelstand#228;ndisches Beratungshaus in Raum Basel suchen wir ab sofort einen Senior Consultant im Bereich Projekt Management. Zu den Aufgaben dieser Position gehand#246;ren unter anderem die Betreuung der verschiedenen Projekte als Projektleiter sowie die Planung dieser Projekte. Weiterhin betreuen Sie bereits bestehende Kunden und arbeiten eng mit den verschieden Teams zusammen um eine best mand#246;gliche Umsetzung der Projekte zu gewand#228;hrleisten. Sollten Sie eine abgeschlossene hand#246;here Ausbildung in einer technischen oder betriebswirtschaftlichen Fachrichtung sowie mindestens 3 Jahre Berufserfahrung als Projektleiter in Pharma oder Medizinaltechnik haben ist diese Position eine grossartige Chance fand#252;r Sie in ein erfolgreiches Unternehmen einzusteigen. Der erfolgreiche Kandidat hat unter anderem auch theoretische Kenntnisse in IT Projektmanagement und beherrscht Deutsch und Englisch in Wort und Schrift fliessend. Sollte diese Stelle von Interesse fand#252;r Sie sein, senden Sie mir bitte Ihren aktuellen Lebenslauf als Word Dokument.Ich arbeite als Recruitment Consultant fand#252;r Real Pharma Schweiz und bin fand#252;r den Bereich Biometriks, HEOR und Market Access innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 43 5080972 oder k.schirmer(at)realstaffing.com zu erreichen.  Keywords: Beratungshaus, Consulting, Projektmanagement, IT, Schweiz, Suisse, Switzerland, PMI, IPMA, OGC, PMP, German, Deutsch, English, Englisch, Baseland#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mitarbeiter in Batch Record Review  Globales Unternehmen  B.W.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB98FFB7C41A5EC9F482579F5001FCC72</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mitarbeiter-in-Batch-Record-Review-and-amp-SHARP150-Globales-Unternehmen-and-amp-SHARP150-B-W_1641303.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein zu einem globalen Konzern gehand#246;rendes Unternehmen in Sand#252;ddeutschland suche ich Unterstand#252;tzung fand#252;r den Bereich and#60;band#62; QA - Batch Record Review and#60;/band#62;Zu den and#60;band#62; Aufgaben and#60;/band#62; gehand#246;ren:and#60;liand#62; Verantwortung fand#252;r Batch Record Reviewand#60;liand#62; Bewertung von Abweichungsberichten, Mediafills u. and#228;.and#60;liand#62; Schnittstelle zwischen QA/ Quality Assurance und Produktion (Salben, Liquida)and#60;liand#62; Bewertung von Qualifizierungsdokumenten (Laborgerand#228;te, Anlagen)Sie sollten folgendes and#60;/band#62; mitbringen and#60;/band#62;:and#60;liand#62; Abgeschlossenes Studium der Pharmazie oder and#228;hnliches naturwissenschaftliches Fachand#60;liand#62; Berufserfahrung im GMP-regulierten Pharma-Umfeldand#60;liand#62; Profundes technisches Verstand#228;ndnisand#60;liand#62; Ausgeprand#228;gte soziale Kompetenz und Teamfand#228;higkeitand#60;liand#62; Strukturierte Arbeitsweiseand#60;liand#62; Gute Englisch-Kenntnisse in Wort und SchriftKlingt das interessant fand#252;r Sie? and#60;band#62;  Ich freue mich auf Ihre Bewerbungsunterlagen und gebe Ihnen gerne mehr Informationen zu dieser und anderen Positionen. and#60;/band#62;Melden Sie sich gerne, auch wenn diese Position nicht genau dem entsprechen sollte, was Sie sich vorstellen.Ich bin spezialisiert auf den Bereich Quality Management und betreue unsere Kunden aus der pharmazeutischen und biotechnologischen Industrie. Sicherlich habe ich auch die passende Stelle fand#252;r Sie.and#60;band#62; Barbara Reist, Real Staffing Group  and#60;/band#62;and#60;band#62; Quality Management and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: b.reist (at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Entwicklungsingenieur für Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob78391A297C7799E9482579F5001FCC7E</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Entwicklungsingenieur-f-and-amp-SHARP252r-Medical-Devices_1641304.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Haben Sie Lust bei der Entwicklung neuer Medizintechnik-Produkte Ihr letztes Wort zu geben? Hier haben Sie die Mand#246;glichkeit Ihre Meinungen durchzusetzen! Mein Kunde aus Baden-Wand#252;rttemberg sucht ein Entwicklungsingenieur fand#252;r die Produktentwicklung. Ihre Aufgaben:- and#220;berprand#252;fung und Validierung von fertigen Medizinprodukten- Konstruktion von Medizinischen Gerand#228;ten- Unterstand#252;tzung bei der  Produktentwicklung (von der Umsetzung der Produktidee bis hin zum Serien-Fertigung)- Aktive Mitarbeit in anderen Bereichen wie Marketing, Produktion und ZulassungIhre Qualifikationen:- Studium in Maschinenbau, Feinwerktechnik oder Medizintechnik ist notwendig- Mehrere Jahre Berufserfahrungen in der Produktentwicklung und Konstruktion sind gewand#252;nscht- Idealerweise Erfahrung mit CAD CATIA V5 Systemen  - Sehr gute Deutsch und Englisch Kenntnisse. Bei weiteren Fragen kontaktieren Sie, Josand#233; Ramand#237;rez Bucheli (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Urgent Senior Process Validation Engineer San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob1C142C6EF26323FC482579F5001FCC93</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Urgent-Senior-Process-Validation-Engineer-San-Diego_1641305.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client in San Diego has an urgent requirement for a Senior Process Validation Engineer with 6 years experience in the Pharmaceutical Industry with the following qualifications:Act as Process Validation subject matter expert for resolution of deviations, assessment of change orders and other quality system actionsOversee/execute selected studies and protocols for processes and systems.Write selected studies, plans, protocols, and reports for processes and systemsQualifications:Education/Experience:BS degree in a scientific discipline with at least 6 years of experience, orMS degree with at least 4 years of related experience.Required Skills/ Knowledge:and#149;Management of complex validation projectsand#149;In depth, working knowledge of 2004 FDA Aseptic Process Guidance for Industryand#149;Solid background and experience with GMPand#146;sand#149;In depth working knowledge of 2011 FDA Process Validation Guidance for Industryand#149;Experience implementing Process Validation Programand#149;Quality Risk Management conceptsThis is an extremely attractive offer that will not be available for long. If interested please send your resume immediately.Keywords: PROCESS VALIDATION, PROCESS ENGINEER, VALIDATION ENGINEER, GMP, DEVIATIONS, CHANGE ORDERS, FDA, QULAITY RISK MANAGEMENT]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[<b> Qualified Person Sachkundige Person <b>  Schwarzwald (m w)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob627382FCDB41CF9A482579F5001FCC9F</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/-and-amp-SHARP60b-and-amp-SHARP62-Qualified-Person-Sachkundige-Person-and-amp-SHARP60-b-and-amp-SHARP62-Schwarzwald-m-w_1641306.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r seinen Produktionsstandort im Schwarzwald sucht mein Kunde eine and#60;band#62; Qualified Person/ Sachkundige Person  and#60;/band#62; (m/ w). Man bietet Ihnen ein and#60;band#62; internationales Arbeitsumfeld and#60;/band#62; und zahlreiche Mand#246;glichkeiten sich weiterzuentwickeln.Zu den and#60;band#62; Hauptverantwortlichkeiten and#60;/band#62; zand#228;hlen:and#60;liand#62; Prand#252;fung und Freigabe der Chargenand#60;liand#62; Sicherstellung der Einhaltung GMP- und anderer relevanter Regularien and#60;liand#62; Produktlaunch und Prozesstransfer and#60;liand#62; Fand#252;hrung von Mitarbeiter. Schaffenand#60;band#62; Ihr Profil and#60;/band#62;:and#60;liand#62; Erfolgreicher Abschluss Pharmazie, Chemie oder verwandtes akademisches Gebietand#60;liand#62; Mehrere Jahre Erfahrung im pharmazeutischen/ chemischen Qualitand#228;tsmanagement und ggf. Galenik, Analytikand#60;liand#62; Ausand#252;bungsberechtigung und idealerweise Erfahrung als QP gem. and#167;15 AMGand#60;liand#62; Fand#252;hrungserfahrung wand#228;re wand#252;nschenswertand#60;band#62; Klingt das ansprechend fand#252;r Sie? Ich freue mich auf Ihre Bewerbungsunterlagen. Erfahren Sie gerne mehr von Frau Barbara Reist. and#60;/band#62;Melden Sie sich gerne bei mir, auch wenn diese Position nicht genau dem entsprechen sollte, was Sie sich vorstellen. Ich bin spezialisiert auf den Bereich Quality Management. Dort betreue ich unsere Kunden aus der pharmazeutischen und biotechnologischen Industrie und betreue ein umfangreiches Portfolio an Festanstellungen und habe sicherlich auch die passende Stelle fand#252;r Sie.and#60;band#62; Barbara Reist, Real Staffing Group  and#60;/band#62;and#60;band#62; Quality Management and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: b.reist (at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interessante Chance für berufserfahrene Quality Manager! (mw)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2E0E3A553BE23413482579F5001FCCAB</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Interessante-Chance-f-and-amp-SHARP252r-berufserfahrene-Quality-Manager-m-w_1641307.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde hat seinen Sitz in Mand#252;nchen und vertreibt Nischenprodukte im Bereich der Ophtalmologie.In Ihrer Funktion als and#60;band#62; Quality Manager and#60;/band#62; and#252;bernehmen Sie die eigenstand#228;ndige Verantwortung fand#252;r alle Prozesse und Belange der Qualitand#228;tssicherung, von der Betreuung des Qualitand#228;tsmanagement-Systems bis hin zur Planung und Durchfand#252;hrung von and#60;band#62; Audits and#60;/band#62;. Weiterhin sind Sie eng in den Zulassungsprozess eingebunden und erfand#252;llen die Funktion des and#60;band#62; Stufenplanbeauftragten and#60;/band#62;.Sie sollten Pharmzeut sein oder ein and#228;hnliches naturwissenschaftliches Studium abgeschlossen haben und bereits Berufserfahrung im GMP-regulierten, pharmazeutischen Umfeld gesammelt haben.Idealerweise, aber nicht notwendigerweise, sind Sie zur Ausand#252;bung der Sachkunde gem. AMG befand#228;higt.Wenn Sie weiterhin bereits Schnittpunkte mit den Abteilungen Regulatory Affairs und/ oder Pharmakovigilanz hatten, ist das ein groand#223;er Vorteil. Das Unternehmen bietet Ihnen ein aufgeschlossenes Team, das eng miteinander arbeitet, einen Bereich, den Sie eigenverantwortlich betreuen und ein and#252;beraus attraktives Gehaltspaket.Klingt das interessant fand#252;r Sie? and#60;band#62;  Ich freue mich auf Ihre Bewerbungsunterlagen und gebe Ihnen gerne mehr Informationen zu dieser und anderen Positionen. and#60;/band#62;Melden Sie sich gerne bei mir, auch wenn diese Position nicht genau dem entsprechen sollte, was Sie sich vorstellen. Ich bin spezialisiert auf den Bereich Quality Management. Dort betreue ich unsere Kunden aus der pharmazeutischen und biotechnologischen Industrie und betreue ein umfangreiches Portfolio an Festanstellungen und habe sicherlich auch die passende Stelle fand#252;r Sie.Ich freue mich von Ihnen zu hand#246;ren! and#60;band#62; Barbara Reist, Real Staffing Group  and#60;/band#62;and#60;band#62; Quality Management and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: b.reist (at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Spezialist in München gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC58F1B9A5FA3D5E2482579F5001FCCBA</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Spezialist-in-M-and-amp-SHARP252nchen-gesucht_1641308.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein innovatives Unternehmen der Medizintechnik suche ich aktuell einen Spezialisten im Bereich Regulatory Affairs. Gesucht werden motivierte und teamfand#228;hige Mitarbeiter, die schon erste Berufserfahrungen sammeln konnten.Ihr Profil:-Kenntnisse von nationalen und internationalen Normen, Gesetzen und Regularien-Erfolgreich abgeschlossenes technisches Studium oder vergleichbare Ausbildung-Sehr gute Deutsch- und EnglischkenntnisseIhre Aufgaben:-Kommunikation zu relevanten Behand#246;rden und Organisationen-Durchfand#252;hrung, Betreuung und Dokumentation von Zulassungen (EMEA)-Optimierung  von Prozessen des RiskomanagementsHabe ich Ihr Interesse geweckt? Dann zand#246;gern Sie nicht, und kontaktieren mich!Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Techniker (mw) Umgebung Saarland gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF9A9C553D6CB04CF482579F5001FCCC5</referencenumber>
<City><![CDATA[Saarland]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Techniker-m-w-Umgebung-Saarland-gesucht_1641309.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62;Mein Kunde, ein mitarbeiterorientiertes Familienunternehmen mit innovativen und anspruchsvollen Produkten, sucht ab sofort einen Quality Assurance Techniker Raum Saarland.and#60;/band#62;Sie haben eine Ausbildung zum Techniker oder ein Ingenieurs-Studium absolviert und konnten bereits mehrere Jahre Berufserfahrung im Qualitand#228;tswesen (Prand#252;fplanung, AQL, SPC) sammeln. Sie verfand#252;gen and#252;ber fundierte Kenntnisse in entsprechenden Tand#228;tigkeiten und Positionen im Bereich Qualitand#228;tsmanagement und haben vorzugsweise eine entsprechende Zusatzqualifikation. Sie sind bestenfalls mit der ISO 13485 vertraut und waren idealerweise bereits im Prand#252;flabor tand#228;tig (Gaschromatograph, FTIR). Sie bringen Wissen in Bezug auf gesetzlichen und normativen Regelungen aus der Medizintechnik mit und beherrschen die englische Sprache in Wort und Schrift verhandlungssicher.Sie sind zustand#228;ndig fand#252;r die Qualitand#228;tssicherung, Prand#252;fplanung und Validierung bei neuen Entwicklungen (Konzeption und Durchfand#252;hrung) und bearbeiten Reklamationen bei technischen Fragestellungen. Sie stellen die Produktqualitand#228;t auf Grund normativer Anforderungen gemand#228;and#223; der technischen Dokumentation sicher und fand#252;hren Dokumentationsprand#252;fungen und Bewertungen durch. Ebenfalls arbeiten Sie im Prand#252;flabor mit. Wenn Sie diese abwechslungsreiche Position in einem modernen, mitarbeiterorientierten Familienunternehmen mit einer lukrativen Verdienstmand#246;glichkeit ansprechend finden, freue ich mich and#252;ber Ihre Bewerbungsunterlagen unter folgenden Kontaktdaten. wydra (at)realstaffing (dot)com Agnes Wydra / Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[REGULATORYQA COORDINATION MANAGER CONTRACT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7874B0057277E3B3482579F5001FCCD1</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/REGULATORY-QA-CO-ORDINATION-MANAGER-CONTRACT_1641310.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[- Ensure that changes to all site documents relating to client requests and information are reviewed and amended via Change Management as appropriate.- Review and approve client artwork for packaging components for compliance with the MA and known labelling legislation.- Member of the site Change Management Review committee in relation to changes affecting client documents and systems.- Liaise with clients in order to obtain Annual Product Quality Reviews and Stability Data and  Technical Agreements in support of Qualified Person (QP) release on site.Expectations and Accountabilities:- To provide day to day regulatory support for all manufacturing operations linked to client products.- To monitor compliance with Manufacturers Licence and individual MAs of Company and clients.- The review and approval of master documents for manufacturing, packaging, Process Amendments and other quality documents as appropriate.- To assist with inspections by external auditors. - To coach and mentor other staff in relation to regulatory requirements.- To resolve regulatory/quality issues relevant to new product introduction, including outsourced manufacture, preparation of technical agreements, documentation, compliance and compatibility with client and site requirements.- To liaise directly with client companies and regulatory bodies concerning regulatory/QA issues.Please call Rachel on 0207 758 7322 asap if you would like to apply for this role and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer 6 Month Contract North West]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob80926C0979B66130482579F5001FCCDE</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Engineer-6-Month-Contract-North-West_1641311.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Develop, generate and maintain documentation to support an effective and compliant Quality Management System, including: Role and#149;Product and Process FMEAs / Risk Assessments and#149;Medical Device Risk Management Reports and Files and#149;Quality Inspection Procedures and Control Plans and#149;Sampling Plans and#149;Material and Product Specifications and#149;Process Flow Charts and#149;Quality Systems and Process SOPs and Work Instructions Experience Requires degree level in Engineering, Microbiology, Chemistry or associated fields, or equivalent industry experience. and#149;Experience in design, manufacturing or quality engineering position (Medical Device experience preferred). and#149;Certified Quality Auditor (essential), Lead Auditor (preferred). and#149;Working knowledge of and experience in developing and manufacturing product in a regulated environment, preferably medical devices to the requirements of cGMP, CFR 21 Part 820, MDD 93/42/EEC, ISO 13458 and ISO 9001. and#149;Will have a fundamental understanding of a quality management system and its development, documentation and implementation. and#149;Will have working knowledge of risk management, risk assessment tools and#38; techniques and reporting in accordance with ISO 14971 (essential). and#149;Clean room experience (preferred). and#149;Certified Six Sigma Green or Black Belt (advantageous). and#149;Experience in review of equipment and process validation deliverables (preferred). Please call Moushmi Patel on 0207 758 7322  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Specialist Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD572E1644090F35B482579F5001FCCE8</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Specialist-Medical-Devices_1641312.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Role -To establish and maintain good relationships with Regulatory Authorities, Regulator colleagues and to support and advice worldwide colleagues -To manage worldwide registration activities. -To ensure product approval and registration is obtained for all new products.by ensuring that all new product dossiers are created. -To ensure that the companies post-marketing surveillance responsibilities Education/Experience - Good first degree in a relevant scientific discipline, or equivalent. - Significant regulatory experience covering medical devices. - Relevant experience of drug-device combination products and/or pharmaceuticals. - Commanding knowledge of worldwide regulatory procedures, especially for medical devices. - Experience gained working in worldwide markets, and able to demonstrate proven track records of achievements - Able to demonstrate projects undertaken have been satisfactorily completed within agreed timescales. - Relevant experience to supervise a Regulatory team to ensure effective contribution and commitment of staff. - Possess computer competency in Microsoft office software, data collection and general analysis tools. Please call Moushmi Patel on 0207 758 7322  and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualitätsbeauftragter (mw) Medizinprodukte Raum Berlin gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD63D80F22B383F52482579F5001FCCF6</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualit-and-amp-SHARP228tsbeauftragter-m-w-Medizinprodukte-Raum-Berlin-gesucht_1641313.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Ein mittelstand#228;ndiges Unternehmen, dass bereits and#252;ber 60 Jahre Marktfand#252;hrer in der Feinmechanik-Optik ist, sucht ab sofort einen and#252;berzeugenden Qualitand#228;tsbeauftragten (m/w) fand#252;r Medizinprodukte Raum Berlin.Ihre Aufgaben:and#149;Aufbau und die Pflege des Qualitand#228;tsmanagement-Systems nach MPG ISO 13485, FDA-QSRand#149;FDA Regularien sowie internationale Zulassung der Produkteand#149;Sicherheitsbeauftragter fand#252;r Medizinprodukte (and#167;30 MPG)and#149;Erstellung und Aktualisierung Technischer Dokumentationen und Vertrand#228;geand#149;Planung und Durchfand#252;hrung interner/externer Audits sowie interner Schulungen and#149;Ermittlung von Qualitand#228;tskennzahlen; Abstimmung von Qualitand#228;tszielen; Ermittlung und Verfolgung von Maand#223;nahmen (CAPA, Qptimierung)Ihr Profil:and#149;Erfolgreich abgeschlossenen im Bereich Physikalische Technik, Maschinenbau oder Mechatronikand#149;Erfahrungen in der Qualitand#228;tssicherung oder der Qualitand#228;tskontrolleand#149;Fundierte Kenntnisse and#252;ber QM-Systeme von Medizinprodukten MPG ISO 13485, FDA-QSRand#149;Erfahrungen bei der Abarbeitung von Recalls als European Quality Representativ sind erwand#252;nschtand#149;Sehr gute Englischkenntnisse in Wort und Schriftand#149;Sie sind team- und kommunikationsfand#228;hig sowie durchsetzungsstark Wenn Ihre letzte Tand#228;tigkeit die benannte Stelleand#132; Sicherheitsbeauftragte fand#252;r Medizinprodukteand#147; gewesen ist und Sie fundiertes Wissen in Bezug auf FDA mitbringen, freue ich mich auf Ihre Bewerbungsunterlagen unter folgenden Kontaktdaten. a.wydra(at) realstaffing(dot)com / Agnes Wydra Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regional Medical Monitor  South East  Global Pharmaceutical]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob34B68F66178B5A09482579F5001FCD02</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regional-Medical-Monitor-South-East-Global-Pharmaceutical_1641314.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Regional Medical Monitor - South East - Global PharmaceuticalThis global pharmaceutical company require a Regional Medical Monitor. The individual will lead the medical oversight of clinical study sites based in their assigned region and neighbouring countries with an emphasis on high medical risk clinical trials.- The RMM must have a medical degree (MD or equivalent) and professional qualification, have previously engaged in medical practice (in an academic, private or government setting), and must have training in ICH/GCP principles.- Deep knowledge of clinical development, and experience in the management and reporting of adverse events and SAEs- Expert in full drug development processes from phase I to IV- Expereince of regulatory audits and requirements- Knowledge of local (and where appropriate) international regulations applicable to clinical development including Ethics Committeesand#146; standards- It is imperative the RMM have experience in Phase 2 - 4 clinical development in the pharmaceutical industry and/or at a CRO, practical experience in clinical trial strategies, methods and processes.- Previous management experience - Strong inter-personal , written/verbal communication skills, ability to evaluate, interpret and present complex dataThe role is in the South East, and is initially a 12 month contract. If you are interested in this role please contact Jessica Warden-Brown on 0207 758 7322 or send an up to date CV for consideration. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior SAS Programmer Oncology  Contract Remote working.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob562AE016216F5319482579F5001FCD0C</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-SAS-Programmer-Oncology-and-amp-SHARP150-Contract-Remote-working_1641315.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My Cambridge MA, pharmaceutical client have an urgent need for a senior SAS programmer with strong Oncology experience to provide statistical programming support for clinical studies and regulatory submissions. Role:You will write programs for the creation of datasets, pooled datasets, tables, listings and figure for clinical trials. You will work closely to specifications and ensure you comply with all programming standards.  You will assist the project team, coordinating all programming activities including regulatory submissions, publications, study reports and informal requests. You will also be expected to support quality control and quality audit of deliverables and establish documentation and archival systems for programming work. Essential Skills:-6+ years SAS programming experience in the Pharmaceutical or Biotech industry-2+ years experience of phase II or III oncology clinical trials   -Expertise in SAS/BASE, SAS/STAT, SAS/MACRO-Competence with SAS/GRAPH, SQL-Experience with regulatory reporting and submissions; involvement in NDA or BLA is preferred-Understanding of regulatory requirements and considerations (e.g. GCP, ICH, 21CFRpart11, CDISC)-Bachelorand#146;s or Masters degree in Statistics, Biostatistics, Computer Science or equivalent work experience To apply for this position please click on the link or send me your resume directly. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Interesting contract position in NDA subm Biostatistics Boston.]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob49C3021E9031252C482579F5001FCD17</referencenumber>
<City><![CDATA[Massachusetts]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Interesting-contract-position-in-NDA-subm-Biostatistics-Boston_1641316.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Are you a contractor looking to work directly on a Phase III submission to the FDA, gain highly niche skills and dramatically boost your employability?  If so I have the perfect opportunity for you.My client, a successful pharmaceutical company based in Boston in submitting its final FDA documents in Q1 of 2013 and requires a Contract Biostatistician to lead on the efficacy and safety reports.  The Contract Biostatistician will be working on a ground breaking drug which looks set to revolutionise this therapeutic area.This role will involve the full spectrum of work that a Biostatistician can encounter including protocol design, SAP development, efficacy and safety analysis.  The successful candidate will be working with clinical staff and SAS programmers to develop the final submission to the FDA.  Candidates for this position must have the following skills and experience:- Minimum Masters Degree in Statistics, Biostatistics or related field- 7+ years experience within Pharmaceutical, CRO or Biotech companies- Previous experience of assisting on NDA or FDA submissions- SAS Programming KnowledgeThe following skills will make a candidate stand out but are not essential:- PhD in Biostatistics, Statistics or related field- Direct NDA submission experience- CRO Work Experience]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance  technical file review for Medical Device company]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB465262B37829C1D482579F5001FCD22</referencenumber>
<City><![CDATA[Netherlands]]></City>
<Country><![CDATA[NETHERLANDS]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-and-amp-SHARP150-technical-file-review-for-Medical-Device-company_1641317.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Quality Assurance and#150; technical file review for Medical Device company Noord- Brabant 60-70EUR all in p. hourIn this role you will advise/ review/ technical files/ documentation of the client and will help the client to receive CE mark.We look for a consultant with:and#149;Proven track record in writing/ reviewing technical documentation for class 2a-2b-3 medical devices according to MDD for the European Marketand#149;Knowledge, experience in FDA 510(k) US market is a plus.and#149;Preferably worked in start up company and for notified body.and#149;Pragmatic, communicative, motivated.Duration of the project is 3-4 months. Submit your resume via the link below for my consideration. Jasna Breko is specialised in QA vacancies within the medical device industry in the Netherlands. +31 0 20 522 1588. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sales & Marketing Manager, PharmaDiagnostics, Basel area]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7DD6E2F718EE0C36482579F5001FCD2D</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Sales-and-amp-SHARP38-Marketing-Manager-Pharma-Diagnostics-Basel-area_1641318.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients is looking to fill the Marketing and Sales Manager position for the pharma / diagnostic division in the greater Basel area.Sales and#38; Marketing Manager, Pharma/Diagnostics, Basel area The company is established in Switzerland for more than 50 years being also internationally represented. The firmand#146;s core industry areas are pharmaceuticals, diagnostics and consumable (food) products. Its location in the greater Basel area offers a place to be for the pharmaceutical industry.The client is looking for a candidate who is familiar with the essential marketing skills like planning and roll-out of marketing processes and branding. Additionally, the candidate would work closely with the sales force and being involved into sales by monitoring, developing and increasing financial accounts (e.g. turnover). Outstanding communication skills and being confident in holding presentations are necessary to promote the diagnostic products. Therefore, a great knowledge as well as experience in this area is essential. For this position an academic degree (e.g. biology, chemistry) is needed. Additionally, being fluent in English and German is important.Requirements:-Academic background (scientific)-Knowledge of marketing, classical skills-Offering past experience in sales and marketing, preferred in diagnostics-Monitoring sales regarding financial as well as performance targets-Know-how of diagnostics / pharmaceutical industry-Great communication skills and being comfortable in holding presentations-English and German fluent oral and writtenYour benefit:The salary for this position is negotiable.Further, the company offers an attractive work environment as well as career opportunities for you. I am Corinna Kutzner, a recruitment consultant working only in Switzerland and specialise for marketing recruitment in Medical Devices/Pharmaceutical industry. If you want to get further information regarding this position, or on many more like it, please do not hesitate to contact me on +41 435080972 or c.kutzner(at)realstaffing.com Key words: Marketing, Pharmaceutical, Zand#252;rich, Marketing and#38; Sales Manager, Switzerland, Consumable Products, Basel, Diagnostics, Market, Roll-out, Flexible, Team Player, Marketing Processes, Marketing Expertise, Baselland, Corinna Kutzner, Marketing and Sales Manager, Diagnostic Products, Sales, Targets, Marketing Tools, Creative]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Passionate Global Product Manager, Pharma, near Zurich]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4E44572D674F190B482579F5001FCD39</referencenumber>
<City><![CDATA[Zurich]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Passionate-Global-Product-Manager-Pharma-near-Zurich_1641319.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of my clients of the pharmaceutical industry is currently looking to fill the position of a Global Product Manager.Passionate Global Product Manager, Pharma, near ZurichThe company is looking for a vibrant professional to fill the global Business Unit offering a background in marketing of the pharmaceutical industry. The candidate the company is looking for should have passion towards financial goal as well as strategic goal setting. Additionally, exceptional communication as well as high self motivation skills are wanted besides being fluent in English and in any other second language, if possible (preferred German or French). The role would include: the classical marketing skills like implementation of the product strategies as well as of the marketing tools and analyzing the market and its competitors. Being able to perform independently projects meaning getting down into project management e.g. by monitoring SWOT analyses and ROI targets. The company is located near Zurich focusing on the pharmaceutical and life science industry being represented in more than 100 countries worldwide. It has several production sides in Europe as well as one in the United States. The location close to Zurich offers a great home next to a vibrant city being closely connected to the pharma and life sciences industry as well as being Switzerlandand#146;s biggest city.What is in for you?You gain an interesting salary package as well as career opportunities!I am Corinna Kutzner, a recruitment specialist in marketing recruitment sector. I am currently working with many organisations in this area only in Switzerland. This means that I can offer you multiple vacancies for your job search. For more information on this, or any other similar roles, please apply online or contact Corinna Kutzner on +41 (0) 43 50 80 972.Key words: Marketing, Pharmaceutical, Product Manager, Switzerland, Marketing Strategies, Zurich, Marketing Tools, Return on Investment, Implementation, Zand#252;rich, English, German, Products, Medical, Life Science, Project Management, ROI, Projects, SWOT Analyses, Roll-Out]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager in Bayern gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob8165FF5223979B5C482579F5001FCD45</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-in-Bayern-gesucht_1641320.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Sie sind auf der Suche nach einer neuen spannenden Herausforderung in einem innovativen und international ausgerichteten Unternehmen?Dann lesen Sie weiterand#133;Aktuell suche ich fand#252;r meinen Kunden, einem wachsenden und zukunftssicheren Unternehmen der Medizintechnik einen Regulatory Affairs Manager.Folgende Qualifikationen sollten Sie mitbringen:and#149;Technische Dokumentationand#149;Risikomanagementand#149;Erstellung und Pflege der relevanten Dokumenteand#149;ISO 13485, ISO 14971, ISO 60601, ISO 10993and#149;Nationale und internationale Zulassungen fand#252;r Medizinprodukte der Klasse I, IIa, IIb and#149;Erfolgreich abgeschlossenes technisches Studium oder vergleichbare AusbildungHabe ich Ihr Interesse geweckt? Dann zand#246;gern Sie nicht, und kontaktieren mich!Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[EDITORIAL TEAM LEAD]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob11FC006F868E02F8482579F5001FCD50</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/EDITORIAL-TEAM-LEAD_1641321.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[One of the most established medical communication agencies in the UK have a fantastic new opening for an Editorial Team Leader within their Cheshire offices. This unique opportunity will require someone to provide their editorial leadership for accounts and take responsibility for the day to day client service and delivery of projects. As the Editorial Team Leader, you will be expected to manage the full range of high-quality medical communication services, whilst utilising your commercial expertise to balance all the elements of project management and writing/editing responsibilities.The successful applicant will take responsibility for briefing all members of the project team on everything from time allocations and target audiences, to clients key messages and timelines/schedules. You will be expected to maximise existing accounts by identifying new opportunities and contribute your efforts to new proposal development and pitches. As the Editorial Team Leader, you must be confident in your ability to proactively drive projects through to completion, and support other Editorial Team Leaders to ensure the best practice across accounts. This role would suit an enthusiastic self-starter who is eager to achieve and has the ability to cope well under pressure. Rewards include a fantastic starting salary and extensive company benefits. You well be welcomed into a hard working but social office environment that offers everything from weekly evening meals out to fancy dress and team building events. Of course, performance related bonuses and special achievement awards are on offer to anyone hoping to build a longstanding career within this group! For more information on this exciting opportunity, contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Systems and Validation Specialist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob558F08EDAF49BCF0482579F5001FCD5B</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Systems-and-Validation-Specialist_1641322.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Pharmaceutical Manufacturer based in Kent is currently recruiting a Quality Systems Leader to ensure that all Quality System activities comply with regulatory and company policies. Reporting to the Quality Systems Manager you will become technically focussed within Quality Systems and Validation to a specialist level in the industry. As the Quality Systems Leader you will:Provide expertise and guidance to user departments in the development of validation strategies and efficient and effective execution of validation and revalidation activities in compliance with Validation policies and procedures. Ensure the Site Validation Master Plan is generated and maintained to policy requirements.Co-ordinates the CAPA processManage the Quality Review Process Provide support to compliant investigationsPrepare activities associated with Regulatory audits of the plant. Ensure Inspection readiness.They are looking to pay up to and#163;40k + Benefits for the right candidate, if you are interested in this opportunity please send an updated CV to John Morkus.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Responsable Assurance Qualité]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobCAE19A7B2964B049482579F5001FCD67</referencenumber>
<City><![CDATA[Paris]]></City>
<Country><![CDATA[FRANCE]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Responsable-Assurance-Qualit-and-amp-SHARP233_1641323.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Rejoignez une sociand#233;tand#233; spand#233;cialisand#233;e dans les dispositifs mand#233;dicaux innovants and#224; dimension internationale en tant que Responsable Assurance Qualitand#233;.Vos missions: Rattachand#233; au Directeur Gand#233;nand#233;ral France sur le site et au Directeur AQ Europe (en fonctionnel), vous conduirez les activitand#233;s suivantes :and#149;Conformitand#233;/complianceand#149;Mise en place et suivi des CAPAand#149;Audits Qualitand#233; Internes et Externes (Qualitand#233; Fournisseur)and#149;Liband#233;ration des produitsand#149;Suivi du Contrand#244;le Qualitand#233;and#149;Gestion des Rand#233;clamations clientsand#149;Validation (produits and#38; process)Vous serez accompagnand#233;(e) dand#146;une and#233;quipe de 5 personnes pour ces activitand#233;s/responsabilitand#233;s pour lesquelles vous serez le rand#233;fand#233;rent lors dand#146;audits et/ou inspections.Votre profil:-Bac +4/5 ou dipland#244;me dand#146;Ingand#233;nieur avec une spand#233;cialisation en Microbiologie-8 and#224; 10 ans dand#146;expand#233;rience dont 4 spand#233;cifiquement dans land#146;industrie des DM de Classe 3 ;-Une bonne maand#238;trise des rand#233;fand#233;rentiels/rand#233;glementations qualitand#233; suivants : FDA, ISO 13485, RIM (Canada), JPAL (Japon) ;-Anglais fluide obligatoire;-Aisance relationnelle et de vraies capacitand#233;s managand#233;riales ;Vous devez obligatoirement justifier dand#146;une expand#233;rience dans les domaines suivants :and#149;Dispositifs mand#233;dicaux de classe 3and#149;Rand#233;fand#233;rentiels de land#146;industrie du DM en vigueur (3-5 ans minimumEnvoyez-moi vite votre CV sous format Word.Je suis Benjamin MAURICE de Real Pharma, cabinet de recrutement spand#233;cialisand#233; dans lindustrie pharmaceutique. Je travaille avec de nombreux clients CRO, laboratoires pharmaceutiques ou biotechs, ce qui me permet de conseiller mes candidats pour les orienter vers des opportunitand#233;s qui rand#233;pondent le mieux and#224; leurs attentes.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CAPA Quality Officer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob64D8E5E54F84DF8C482579F5001FCD73</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CAPA-Quality-Officer_1641324.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leading Pharmaceutical Manufacturer based in the South East easily commutable from London, Maidstone and Dartford are currently a CAPA Officer to manage all CAPA documentation within the respective manufacturing facility. Reporting to the Quality Assurance Manager for site production you will have the following responsibilities: -Maintain and document proper compliance and quality systems requirements. -Provide subject matter expertise in CAPA and serve as the departmentand#146;s primary point of contact in processing, monitoring, reporting, and resolving problems and process improvements. -Work with the QA Manager to establish strategic direction for CAPA activities to ensure that they are aligned with the business and quality initiatives and in compliance with all regulatory requirements. -Maintain and manage positive working relationships and ensure appropriate representatives from affected departments are involved while assisting in all stages of CAPA management and resolution. -Ensure and monitor that adequate training is performed and competency is maintained among all CAPA department staff. Maintain personal competency in all aspects of CAPA, including policies and procedures. -Guide and direct the CAPA functions by means of staff performance feedback, evaluation and development to ensure CAPA staff understand and are competent to perform their roles and responsibilities and are in compliance with required procedures and all local and federal regulatory requirements. If you are interested in this position you must have:-Previous education within scientific, technical or related discipline, MS preferred. -Previous experience working in quality, with experience in CAPA processes including investigations, technical writing, documentation, and use of statistical tools/techniques is required. -Basic knowledge of MHRA regulations and ISO standards. -Prior experience in manufacturing environment.Though this position has a manager title it does not have any direct reports, as a result this is a great opportunity for a Quality Officer looking to get involved in a position of authority across the manufacturing department. Salary is up to and#163;25k including benefits; if you are interested please send an updated CV to John Morkus.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Leiter Regulatory Affairs gesucht  BadenWürttemberg]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob76F15313704FA774482579F5001FCD7E</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Leiter-Regulatory-Affairs-gesucht-and-amp-SHARP150-Baden-W-and-amp-SHARP252rttemberg_1641325.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein internationales Unternehmen der Medizintechnik suche ich aktuell einen Leiter Regulatory Affairs. Wenn Sie auf der Suche nach einer neuen Herausforderung mit spannenden Produkten und Aufgaben sind, dann lesen Sie weiterand#133;Folgende Qualifikationen sollten Sie mitbringen:-Abgeschlossenes technisches Studium oder vergleichbare Ausbildung-Einschland#228;gige Berufserfahrung in dem Bereich Regulatory Affairs-Nachweisbare Fand#252;hrungserfahrung oder Fand#252;hrungspotential-Kenntnisse von Normen, Gesetzen und Regularien fand#252;r Medizinprodukte-Kommunikationsfand#228;higkeit und Durchsetzungsvermand#246;gen-Durchfand#252;hrung, Betreuung und Dokumentation von Zulassungen-Verhandlungssichere Deutsch- und EnglischkenntnisseWenn ich Ihr Interesse geweckt habe, dann zand#246;gern Sie nicht und kontaktieren Sie mich. Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Medical Advisor in der Klinischen Forschung im Norden gesucht]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob954FADE0C485FF45482579F5001FCD8B</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Medical-Advisor-in-der-Klinischen-Forschung-im-Norden-gesucht_1641326.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;band#62; Medical Advisor in der Klinischen Forschung im Norden gesucht (m/w) and#60;/band#62;Sie sind Mediziner? Und sind in der Industrie tand#228;tig? Dann kand#246;nnte Sie folgendes interessierenand#133;Fand#252;r ein international agierendes Pharmaunternehmen suche ich im Norden Deutschlands einen and#60;band#62; Medical Advisor (m/w) and#60;/band#62;!Hier erwarten Sie u.a. folgende and#60;band#62; Tand#228;tigkeiten and#60;/band#62;:and#60;liand#62; Betreuung von Klinischen Studienand#60;liand#62; Mitarbeit in der Pharmakovigilanz, wie die Verantwortung der medizinischen Inhalte von den Patienten und deren Sicherheit und das Schreiben von Clinical Expert Reportsand#60;liand#62; Beantwortung von medizinischen Anfragen externer Kundenand#60;liand#62; Schreiben von CTD Modulen und Pediatric Investigational PlansSie wand#228;ren in der medizinischen Abteilung und wand#252;rden sowohl Aufgaben aus der Klinischen Forschung, der Pharmakovigilanz und der Regulatory Affairs Abteilung and#252;bernehmen.Fand#252;r diese Stelle sollten Sie folgende and#60;band#62; Eigenschaften and#60;/band#62; nachweisen kand#246;nnen:and#60;liand#62; Abschluss eines Medizinischen Studiumsand#60;liand#62; praktische Erfahrung im Bereich der Klinischen Studienand#60;liand#62; Kenntnisse mit dem MedDRA-Codingand#60;liand#62; flieand#223;endes Englisch in Wort und Schriftand#60;band#62; Klingt das ansprechend fand#252;r Sie? Wir freuen uns auf Ihre Bewerbungsunterlagen. Erfahren Sie gerne mehr von Frau Hanna Holowaty. and#60;/band#62; Falls diese Rolle nicht genau dem entsprechen sollte, was Sie sich vorstellen, dann wenden Sie sich dennoch gerne an mich, Ich bin spezialisiert auf die Pharmakovigilanz sowie den Medical Affairs Bereich. Dort betreue ich ein weitreichendes Portfolio an Festanstellungen und habe sicherlich auch die passende Stelle, mit der Sie Ihre berufliche Situation optimieren kand#246;nnen.and#60;band#62; Hanna Holowaty, Real Staffing Group  and#60;/band#62;and#60;band#62; Medical Affairs/ Pharmakovigilanz and#60;/band#62;Tel.: +49 (0) 69 264 89 8400 E-Mail: h.holowaty(at)realstaffing.comand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Qualified Person  South East]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6493C0808F0B5384482579F5001FCDA2</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Qualified-Person-South-East_1641327.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Based in the South East One of the UKand#146;s fastest growing Pharmaceutical companies is currently look to hire a new QP for the Head Quarters in Kent. Based in the South East you will be in charge of all commercial batch release and on site Quality Systems Projects.  Reporting directly to the Senior Management Team you will be responsible for all aspects of Quality Assurance and QP release. As the Qualified Person you will:You will ensure first class Standard Operating Procedures.Establish the Quality Management System for documentation, customer complaints, deviations, distribution, supply chain and internal audits.You will be named QP release on products imported inside the EU and from the US.You will work alongside the Global Quality Team based in Europe.Act as an operational quality specialist advising all departments.  Be responsible for a regulatory inspections and customer audits. Offer support to the Pharmacovigilance team on customer complaint procedures.Recruit further quality staff to the department. To apply you must:Have fantastic experience of GMP and Regulatory Standards within PharmaceuticalsHave previous held a position of managementPrevious experience in a fast paced environmentBe able to demonstrate excellent communication skills and problem solving abilityThis position based in the Midlands is looking to offer a great salary and benefits scheme. If you are interested in the position, please send an updated CV to John Morkus the Head of Quality Assurance Recruiter. Keywords: Quality Assurance Auditor, Quality Assurance Officer, Internal Audit, External Audit, Quality Systems, Quality Management Systems, QMS, Compliance, QP, Qualified Person, Responsible Person.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR MEDICAL WRITER]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA68D98B65D5F1378482579F5001FCDAF</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/SENIOR-MEDICAL-WRITER_1641329.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Pharma have an outstanding opportunity for a Senior Medical Writer. You must be driven, proactive and have a science background. You will be looking to expand your knowledge and skills within the Medical Communications Industry. The company is based just outside London. They value their employees and possess a strong work life balance approach. They are looking for a person who has a scientific background and is eager to combine medical writing and project management skills. You will oversee key projects whilst being very hands on with the creation of articles, presentations and scientific documentation.Are you a keen medical writer who doesnand#146;t want to be tucked away in an office just writing?Do you want to be involved in all aspects of a project?Are you an enthusiastic go-getter?If this could be the role for you, please contact Rebecca Randles on 0207 758 7311.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ORMC Oncology MSL]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob06046D01EFCDD66E482579F5001FCDBC</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ORMC-Oncology-MSL_1641330.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Liaising with internal and external stakeholders to exchange scientific data relating to the Oncology/ Haematology field-Responding to off-label requests from clinicians-Working on medical education activities at regional level-Staying up-to-date with all relevant clinical data/ publicationsIf this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Experienced Medical Science Manager]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD5CB296242AD64C3482579F5001FCDC9</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Experienced-Medical-Science-Manager_1641331.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilitiesand#149;The person who fills this role will be expected to maintain and develop relationships with KOLs, participate in coordinating and conducting peer-to-peer interactions and medical presentations, and serve as a reviewer for independent research initiatives and publications. and#149;They will represent Medical Affairs at national and international meetings, congresses and symposiums. Reviewing promotional materials to ensure the materials adhere to the ABPI Code of Practice and reviewing submissions and formulary applications will all be part of the role. and#149;The MSM will also be expected to work with cross-functional colleagues in sales, marketing, market research, training, health economics, clinical operations and external affairs. and#149;They will build solid and credible relationships with the medical community on the companyand#146;s behalf and cultivate key thought leaders and product advocates in the Academic and Community settings. If this role interests you please email me.Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison, pharmaceutical, Pharmaceutical, medical, science, medical science liaison, medical affairs, medical science liaison, MSL, KOL, medical science liaison and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Pharmacovigilance Associate  Cambridge  £30,000 circa]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE781576791B84842482579F5001FCDD6</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Pharmacovigilance-Associate-Cambridge-and-amp-SHARP16330000-circa_1641332.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a niche pharmaceutical company with an excellent reputation.With a need to tend to a demanding workload, there is a position available as Pharmacovigilance Associate.While the main responsibility consists of AER related activities, there will be an opportunity to learn and perform various functions within the pharmacovigilance model.Consistent quality in case processing and an aptitude to take on new knowledge are the main attributes sought for the right candidate.Open to UK/ EU permitted workers only - please do not apply if you do not currently hold the right to work within the EU.If you would like to apply, please send your updated CV to Taran Jefferson -  t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[ORMC Diabetes SAM]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF519F44E93C790AB482579F5001FCDE1</referencenumber>
<City><![CDATA[Uk Wide]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/ORMC-Diabetes-SAM_1641333.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Accountabilities-Assessing research articles and reports related to company products and potential future product development. -Rating opportunities for Investigator Initiated Trials -Building credible KOL relationships-Represent the company to world leaders in Diabetes care and research-Understanding regulatory compliance and FDA requirements for the Medical Device industry as they relate to the companyand#146;s products-Providing information and recommendations to Rand#38;D and other departments to monitor reactions related to the companyand#146;s Diabetes products-Coordinating regional education and scientific symposia-Ensuring advocacy, clinical knowledge, and proper training on company products with KOLs and academic centers.-Understanding the difference between making recommendations in therapy based on validated standards of clinical affairsIf this role interests you please email me.Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East, Scientific Affairs Manager, Medical Science Liaison, Diabetes, KOL, South-East and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs  Medical Devices  £40k  Yorkshire]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob71191F06BBA23D8D482579F5001FCDED</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Medical-Devices-and-amp-SHARP16340k-Yorkshire_1641334.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A great opportunity at a global organisation to develop ubternally and upskill on all elements of medical devices, IVDs and Class I to IIIs.Interact with over 100 countries and deal with over 50 different submittal processes.Wound care experience would be a huge advantage as well as experience with a wide range of medical products.The perfect candidate would have worked for a number of years in a regulated environment with at least 2 within Medical DevicesWill be working cross functionally with a number of teams and submittal teams into different global areas. There are a number of opportunities internally depending on the way in which the company grows over the next couple of years.You will be a part of a small team with the opportunity to put your own name on your work and be given the opportunity to develop teams. If you are interested please call on 020 7758 7311 and return your CV to this advert.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Erfahrener Regionalleiter mit dem Schwerpunkt Dermatologie gesucht !!!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA594DACD429E3D12482579F5001FCDFB</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Erfahrener-Regionalleiter-mit-dem-Schwerpunkt-Dermatologie-gesucht-_1641335.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r unseren Kunden, en mittelstand#228;ndiges Unternehmen, welches im Raum Dresden ansand#228;ssig ist suchen wir schnellstmand#246;glich einen erfahrenen Regionalleiter mit dem Schwerpunkt Dermatologie in der Region Nord/West. Unser Kunde legt einen hohen Wert auf soziale Leistungen, die persand#246;nliche Atmosphand#228;re und ist in einen internationalen Pharmakonzern stark eingebunden.   Ihre Aufgaben fand#252;r diese neue Herausforderung sind:-die and#220;bernahme der Umsatzverantwortung fand#252;r die Region -Fand#252;hrung, Training und Coaching der Mitarbeiter - Marktanalyse und die daraus resultierende Ableitung vom Maand#223;nahmen zur    Umsatzsteigerung      -      Planung, Steuerung und Kontrolle der administrativen Aufgaben und          organisatorischen Prozesse       -      Mitwirkung an der Entwicklung und Realisation von Marketingmaand#223;nahmen        Auswahl und Einarbeitung der MitarbeiterWas fand#252;r Anforderungen Sie dafand#252;r erfand#252;llen mand#252;ssen? Ganz einfach, Sie sind fuehrungserfahren, haben bereits ihre Erfahrung in der Dermatologie sammeln kand#246;nnen, verfand#252;gen and#252;ber gute Kenntnisse im Umgang mit MS Office, besitzen gute Englischkenntisse in Wort und Schrift und bestechen durch Ihre kommunikative Kompetenz sowie Durchsetzungsfaehigkeit und Teamgeist.   Sie finden sich hier in dieser Anzeige wieder? Dann kontaktieren Sie mich!Lisa Schumacher I Recruitment ConsultantMarketing and#38; Sales Real Staffing GroupRecognising talentand#38;#61595;and#38;#61472;Taunusanlage 18, 60325, Frankfurtand#38;#61480; Tel:  +49 (0) 69 264 89 8400      Fax: +49 (0) 69 264 89 8001and#38;#61692; www.realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mehrere Gebietsmanager Epilepsie fuer verschiedene Gebiete in der Phar]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob78882A530CB78D1F482579F5001FCE06</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mehrere-Gebietsmanager-Epilepsie-fuer-verschiedene-Gebiete-in-der-Phar_1641336.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Unser Kunde, ein mittelstaendiges Pharmaunternehmen in Frankfurt sucht zum naechstmoeglichen Termin einen erfahrenen Gebietsmaager fuer den Bereich Epilepsie. Haben Sie bereits ein abgeschlossenenes, fachrelevantes Studium im Bereich Naturwissenschaften oder eine erfolgreiche Karriere in der Pharmaindustrie nachzuweisen?Liegen Ihre Staerken in der Beratung und in dem Verkauf von Pharmaprodukten?Haben Sie ein hohes Engagement und eine hohe Kundenorientierung?Dann bewerben Sie sich bei mir fuer die genannte Stelle! Ihre Aufgaben in Ihrem neuen Lebensabschnitt werden die folgenden sein:-Die Pflege unserer Kontakte und die Neugewinnung dieser-Eigenstand#228;ndige Initiierung und Durchfand#252;hrung von anspruchsvollen Fortbildungsveranstaltungen-Sie Bilden neue Netzwerke zwischen Meinugsbildnern, ZIelaerzten sowie Patientenorganisationen-Vertrieb von verschiedenen Produkten bei der relevanten Zielgruppe niedergelassenen Fachaerzten und Klinikaerzten Bei Interesse erreiche nSie mich unter folgenden Kontaktdaten: Lisa Schumacher I Recruitment ConsultantMarketing and#38; Sales Real Staffing GroupRecognising talentand#38;#61595;and#38;#61472;Taunusanlage 18, 60325, Frankfurtand#38;#61480; Tel:  +49 (0) 69 264 89 8400      Fax: +49 (0) 69 264 89 8001]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Searching for 3 Brand Manager with expertise in the Pharma industry]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob3A64CBFE33931091482579F5001FCE14</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Searching-for-3-Brand-Manager-with-expertise-in-the-Pharma-industry_1641337.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a global palyer within the Pharma industry, specialising in the development of innovative medication. Currently they are searching for 3 Brand Managers.The location of ym client is in Hmaburg, this would also be the region where the vacancies are based.Brand Manager RX, PainYour Profile:You have 3-4 years experience in the pharmaceutical industry, with particular emphasis in the sector of Pain therapy (RX)Brand Manager OTCThis position entails you to work within the area of respiratory illnessesYour Profile:You have 3-4 years experience, ideally in an international company specialising in OTCBrand Manager OTC (2)You will be part of an dynamic and international team in the newly developed subsidiary located in North and West of Europe - your main base would be in HamburgYour Profile:3-5 years experience in consumer marketing/product management, ideally acquired in an international environmentGood knowledge in German would be beneficialFluency, both written and verbal, in EnglishThe Position (for all three)Development of market strategiesMarket share growthDevelopment and implementation of (Verbraucher-Verbindungen) - arbeiten fpr einem lokalen Aktivierungsplan und Entwicklung von Pand#228;nenYour are responsible for the development of the market portfolio in the area of branding and for network acquisitionGeneral ProfileCompleted business degree3-5 years work experience, specifically in consumer marketing, product management within the pharma industryGood knowledge of, and work experience within the Scandinavian market (Sweden and Denmark)Good knowdlege, written and verbal, in English. Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Head of Quality Assurance  £75k]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobFE46D16CA6EA284C482579F5001FCE1F</referencenumber>
<City><![CDATA[Wales]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Head-of-Quality-Assurance-and-amp-SHARP16375k_1641338.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Head of Quality Assurance - and#163;75k A multinational healthcare organisation who is based in South Wales is currently recruiting a new Head of Quality Assurance. This organisation specialises in Sterile Liquid Manufacturing and they are actively seeking a new Quality Leader. Heading up an onsite team of 10 you will manage all Quality Assurance and Compliance as well aligning corporate Quality Assurance to site practice. You will report directly to the Director of Quality Assurance and will have impact into the overall QMS. As the Head of Quality Assurance: -Manage site Quality Assurance -Implement continuous improvement in the quality system within the plant-Act as the point of contact for Quality Assurance for external stakeholders and regulatory bodies, including audits, projects and data. -Report directly to the Plant Manager -Liaise with EMEA quality control-Implement Quality System through implementation of robust procedures-Act as Qualified Person for the release of Pharmaceutical productsTo be eligible for this position you must: Have experience in manufacturing and quality control managementHave an excellent understanding of GMP standards.Experience in lean manufacturing techniquesDegree in life science or engineering or equivalent experienceThis is role is an excellent opportunity for any Quality Manager looking to take their first Head of Quality position. They are also offering great benefits and a salary up to and#163;75k. If you are interested in this opportunity please respond with an updated CV to John Morkus and#150; Head of Quality Recruitment.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance Manager London]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5E75F31278210160482579F5001FCE2D</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-Manager-London_1641339.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a UK based manufacturing organisation that is looking to improve their QMS and improve Quality Standards across the business by hiring a New Quality Assurance Manager. As the Quality Assurance Manager you will be responsible for the Quality Management System (QMS) to ensure they are regulatory compliant in all the markets in which we operate. You will also ensure that the business delivers to the consumer a product that meets with the quality and safety standards in all our operating centres.Your responsibilities as Quality Manager will be: To consistently oversee manufacturing, packaging, labeling, and holding operations in the production of products to ensure that these functions are performed in a manner that prevents adulteration and misbranding of finished products.To be responsible for overseeing that all products meet specifications for identity, purity, quality, strength, composition and compliance management. To maintain all aspects of Quality Assurance/QMS in support of relevant site activities to ensure compliance with the requirements of BS EN ISO 9001 for Quality Standard, and the Companyand#146;s continued accreditation. To conduct periodic internal audits of the entire plant, as well as satellite facilities, with documented corrective actions kept on file. To review and approve all master manufacturing records, and all modifications to the master manufacturing records.  To review and approve all batch production-related records, including all records for packaging and labeling operations, ensuring that production records are reviewed for completion and errors. To act as the Qualified Person to release products for distribution in UK and overseas markets, ensuring that products are safe and conform to the quality standards.To be eligible to apply you must: Previous GMP Experience Eligible to release commercial material as a Licensed QPExperience managing projects and teamsPrevious experience of Quality Assurance Management This is a fully functioning manufacturing facility with packaging and a production site of 200. If you wish to work in a continually improving environment in a role which will allow you to imprint Quality Standards from the offset this is an excellent opportunity for you. If you wish to apply please send an updated CV to John Morkus Head of Quality Assurance recruitment or call 0207 758 7311 for further details.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Jr. Bioinformatician Needed for NYC StartUp  up to 80K!]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC4B5B63343047124482579F5001FD061</referencenumber>
<City><![CDATA[New York]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Jr-Bioinformatician-Needed-for-NYC-Start-Up-up-to-80K_1643031.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Start-up Diagnostics company in NYC seeking a Jr. Bioinformatician to join newly developed Bioinformatics division.  Opportunity to join a rapidly growing company in a high-demand industry in the middle of New York City.  Great benefits on top of a competitive salary!Main responsibilities:- Genetic data analysis- Prgramming/database work- Web application developmentNecessary Skills:- Gene expression/analysis- knowledge of R bioconductor- understanding of broad range of databases- microarray analysis/diagnostics- SQL server, .NETEducation:BS in Life Science OKMS in Bioinformatics, Life Science, or similar a PLUSRecent grads OK!If interested, please apply now or call Marco Santa Maria at 212-707-8499.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produktmanager  Medizintechnik]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE0C832F4AA9149E9482579F5001FD06C</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Produktmanager-and-amp-SHARP150-Medizintechnik_1643032.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Fand#252;r ein fand#252;hrendes Unternehmen suche ich ein spezialisierter Produktmanager mit Erfahrung in der Notfall- und Intensivmedizin. Ihr Aufgabengebietand#149;Konzeption neuer sowie Weiterentwicklung bestehender Produkte and#149;Kundenland#246;sungen auf der Basis von Marktanforderungen und Kundenwand#252;nschenand#149;Verantwortung fand#252;r die Produktionseinfand#252;hrung von Medizinproduktenand#149;Integration von Zulieferprodukten in unsere Produkt- und Dienstleistungenpaletteand#149;Verantwortung fand#252;r die Ausrichtung der Medizinprodukteand#149;Beobachtung und Analyse der Mand#228;rkte und Wettbewerberand#149;Erstellung technischer Konzepte und Spezifikationen fand#252;r medizinische Gerand#228;teIhr Profiland#149;Abgeschlossenes Studium (Medizintechnik, Wirtschaftsingenieurwesen o. and#196;.)and#149;Kenntnisse im Bereich der klinischen Medizintechnik sind wand#252;nschenswertand#149;Erfahrung im Rettungsdienst oder mit Notfallmedizin ist erforderlichand#149;Erfahrungen im Bereich wissenschaftlichen Arbeitens zur Betreuung und Erstellung klinischer und/oder prand#228;klinischer Studienand#149;Reisebereitschaftand#149;Sichere Englischkenntnisse in Wort und SchriftHaben wir Ihr Interesse geweckt?Dann freuen wir uns darauf, Sie kennen zu lernen. Ihre Bewerbung senden Sie bitte an s.schaefer(at)realstaffing.com Ihre Fragen zur Position beantwortet Ihnen Frau Schaefer gerne unter Telefon: +49 (0) 69 264 89 8400. Wir freuen uns auf Ihre Kontaktaufnahme! and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Business Development Manager Elektrophysiologie]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB90F835332DFA812482579F5001FD079</referencenumber>
<City><![CDATA[Berlin]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Business-Development-Manager-Elektrophysiologie_1643033.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Art der Tand#228;tigkeit: PermGehalt: Nach QualifikationOrt: BerlinSie sind auf der Suche nach einer neuen Herausforderung und mand#246;chten dabei fand#252;r ein internationales Medizintechnik Unternehmen arbeiten? Dann sind Sie bei mir an der richtigen Adresse! Einer meiner Kunden sucht zum nand#228;chst mand#246;glichen Zeitpunkt einen Business Development Manager der den bestand#228;ndigen Wachstumspfad des Unternehmens weiter fortfand#252;hrt.Ihre Tand#228;tigkeiten:and#149;Aktiver Ausbau des Internationalen Wachstums im Bereich der Elektrophysiologie.and#149;Unterstand#252;tzung von Tochtergesellschaften und Hand#228;ndlern bei der Etablierung von Geschand#228;ftsmodellenand#149;Planung von strategischen, taktischen und operativen Maand#223;nahmenand#149;Prand#228;senz und Prand#228;sentation auf Internationalen Kongressen Die Anforderung:and#149;Abgeschlossenes Studium der Medizintechnik, Betriebswirtschaftslehre oder vergleichbare Fachrichtungen and#149;Idealerweise Erfahrungen im Bereich Business Development und MBAand#149;Marketing und Vertriebserfahrung im Bereich Elektrophysiologie und/ oder im Umfeld des Herzkatheterlaborsand#149;Sehr gute Englischkenntnisse gepaart mit weitern Fremdsprachen, z.B. Spanisch, Franzand#246;sisch, Portugiesisch, Italienischand#149;Sie bringen hohe internationale Reisebereitschaft, hohe Eigenmotivation  und eine zielorientierte Arbeitsweise mit. Fand#252;hlen Sie sich angesprochen und sind Sie bereit fand#252;r eine aufregende Tand#228;tigkeit?Dann bewerben Sie sich umgehend. Fand#252;r weitere fragen steht Ihnen sehr gerne Herr and#214;ztand#252;rk zur Verfand#252;gung.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical SAS Programmer  Illinois  Contract  Pharma]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE81DDD1B41CBBF89482579F5001FD087</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-SAS-Programmer-Illinois-Contract-Pharma_1643034.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client, a leading global Pharmaceutical Company in Illinois, currently has an urgent opening for a Clinical SAS Programmer.  The Clinical SAS Programmer will work on a variety of projects across Phases II and III of Clinical Trials.  This is a 12 month contract paying and60 - and70 per hour.This leading company is seeking a talented Clinical SAS Programmer to create the Tables, Listings and Graphs for a number of Clinical Study Reports (CSR) for Phase II and III studies across a variety of Therapeutic Areas.  IN addition, based on the success of the studies, the successful candidate will have the opportunity to work on NDA submissions.To be suitable for this great opportunity, candidates must have the following skills and experience:- Bachelors Degree or above within Computer Science or related field- 3+ years experience within the Pharmaceutical Industry- Proven track record of creating Tables, Listings and Graphs for Clinical Study Reports- Track record of working closely with multi-disciplinary teamsApply now for immediate consideration or contact Tom Bakker on 312-453-9088. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Balloon Catheter Engineer]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE8C1DFA0AA57748C482579F5001FD092</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Balloon-Catheter-Engineer_1644976.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Calling all Balloon Catheter Engineers!Real Staffing Group is urgently seeking a Senior Balloon Catheter Engineer for a Leading Medical Device company in the Bay Area. This ground breaking medical device company is looking to bring on a full time employee with a strong engineering and design background with experience in the medical device fieldRole: As a Senior Rand#38;D Engineer, you will be responsible for the full life cycle design and development of balloon catheter components, as well as related testing and analysis for product and systems. Essential skills and qualities include project planning and management, cross-functional communication between design team and board members, and ability to independently perform assignments as well as give technical guidance to lower level personnel.Requirements:B.S. in Engineering (Mechanical Engineering desirable)6+ years of engineering experience in regulated field4+ years of Medical Device experienceMust have experience with Balloon Catheter designLeadership capabilitiesStrong communication skillsSalary:and85-110k depending on experienceIf you are passionate about the medical device industry please send me an updated resume and I will follow up with you. Thank you and be in touch.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CRA  Monitoring opportunity home and officebased]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC33B1ACA3B3456EF482579F5001FD09D</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CRA-Monitoring-opportunity-home-and-office-based_1644977.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[For my client, a big international CRO with several sites in Germany, I am looking for a CRA or Senior CRA for offices in Central or South Germany or home-based office.Your responsibilities: and#149;Monitor visits (pre-study, initiation, monitoring and close-out)and#149;Site managementand#149;Protocol writingand#149;tracking of CRFsand#149;co-monitoring and training visitsYour experiences:and#149;min. 1 year monitoring experienceand#149;therapeutic and protocol knowledge and#149;fluent in German and Englishand#149;knowledge in clinical studiesIf you are looking for challenges and interesting clinical studies,  then I am looking forward to your application, including your CV. For questions and more information, do not hesitate to contact me:Yana ZinchukReal Staffing+49 (0)69 264 89 8400 y.zinchuk(at)realstaffing.com and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Trials Assistant with an international CRO]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0F305A7039202565482579F5001FD0AB</referencenumber>
<City><![CDATA[Germany]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Clinical-Trials-Assistant-with-an-international-CRO_1644978.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is a privately owned medium sized CRO with a global reach and a strong presence in the emerging markets of Asia Pacific, Middle East and#38; Africa and Eastern and#38; Central Europe. At the moment I am looking for Clinical Trials Assistant (CTA) or Junior Clinical Research Associate (Junior CRA), office based and full time.Requirements: + Life Science Degree or equivelant OR equivalent healthcare experience+ IT skills+ Strong organizational and communication skills+ fluent German and EnglishFor more information please do not hesitate to contact me.E-Mail: y.kamenova(at)realstaffing.comTel.: +49 264 898 400I am looking forward to hearing from you soon.Kind regards,Yuliyana Kamenova and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Orthopaedic Sales Specialist Medical Devices]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob6240FA27891CAF7F482579F5001FD0B7</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Orthopaedic-Sales-Specialist-Medical-Devices_1644979.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A Sales Representative is urgently needed to be active within the region of Baveria. My client develops and manufactures instruments and implants for sports medicine and the orthopaedic industry. The company is an SME, with more than 40 years experience within the medical device industry and is therefore a respectable player within the orthopaedic market.The vacancy entails you to perform the following tasks:and#149;Active within field salesand#149;Client consultingand#149;Client additionand#149;Overall business developmentand#149;Attending and presenting at medical device specific fairsand#149;Presenting the company at eventsYour Profile:and#149;A successful completion of a business-related Degree, or numerous years experience in the field of salesand#149;Several years experience in the overall market concerning and#147;Medical Devicesand#148;and#149;Problem-solving and leadership characteristicsand#149;Fluent, both verbally and written in Germanand#149;Follow a confident worth ethicand#149;Strong communication skillsand#149;Experience and knowledge with orthopaedic products and industryand#149;Clientele base already developed in southern Germany would beneficialAdditionally, the position brings with it an attractive salary package.Do you recognise yourself? Then do not hesitate to send me your CV, to get further details. Your contact person is Simone Schaefer, email:  s.schaefer(at)realstaffing.com. Contact number: +49 (0) 69 264 89 8400   and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Regulatory Affairs Specialist (Diagnostics Device)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD4FA3D973D2AF9D8482579F5001FD0C3</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Regulatory-Affairs-Specialist-Diagnostics-Device_1651694.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our client is an international life sciences (diagnostics) company seeking an experienced regulatory affairs specialist/senior specialist for their growing team. The ideal candidate will be involved in the following areas:- Prepares timely submissions, amendments, supplements, annual reports and other regulatory documents - Interfaces with other departments to provide Regulatory advice and obtain the necessary documents and draft reports and components in accordance with regulatory agenciesand#146; guidelines.-Prepare and submit PMA and/or 510(k)s (FDA) and/or International submissions experience to obtain regulatory clearances for new products and product changes in a timely manner.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Director of Regulatory Affairs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2E05B2437A840918482579F5001FD0CF</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Director-of-Regulatory-Affairs_1651695.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Our client is a well-established pharmaceuticals company in the San Francisco Bay Area, seeking a Director of Regulatory Affairs. The ideal candidate have the following responsibilities:-Ensure all IND and NDA (505b2) submissions and amendments and supplements are completed-Prepare submissions in CTD/eCTD Format-Interpret and communicate all current FDA requirements and guidelines and communicate to both senior and peer management-Interacting with ex-US regulatory authorities, with an emphasis on EMA]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Marketing SpecialistSan FranciscoManaged Care]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobADC86B43F39EF18B482579F5001FD0DC</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Marketing-Specialist-San-Francisco-Managed-Care_1651696.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A leader in the biotech/pharma space specializing in the cardiovascular space is looking to expand their team of Managed Care Marketing professionals. This company has clear avenues for career progression and leadership opportunities. As the managed care marketing manager you will report directly to the Senior Director Managed Care Marketing.  The Role: -Highly analytical role (quantitative data) serving as a liaison cross functionally with clinical, regulatory, market access, and health economics. -Responsible for packaging data and reimbursement strategy for field reimbursement professionals in efforts to support payer relations, coding, and coverage -Private payer market research- payer roundtables/ad boards, synthesis of data and summarizing results for internal and external use-Deliver presentations, power points, and value propositions pertaining to managed care marketing projects]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer , Medical Device  San Diego; excellent rate an]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob380D97FF285D7259482579F5001FD0F1</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Medical-Device-and-amp-SHARP150-San-Diego-excellent-rate-an_1651697.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Responsibilities and Duties:-System development, compliance and regulatory functions-Internal/supplier audits-Design inputs, components, processes-Supervision of quality system-Inspection techniques-Acceptance sampling plansRequirements:-six sigma-lean manufacturing-TQM-Inspection criteria-Excellent written and communication skills-Highly organized-Team workThis is an excellent opportunity with a company that offers paid vacations, fantastic benefits, and a great work environment. It is urgent so if you are interested and think you are a good fit, send your resume at your earliest convenience.Keywords: QA, Quality engineer, Audits, six sigma, compliance, design, inspection]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Product Validation Engineer  San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC682AD48D00B42FB482579F5001FD0FF</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/URGENT-Product-Validation-Engineer-San-Diego_1651698.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My Client has a need for a Product Validation Engineer to handle the validation tasks assigned in the lifecycle phases on the Design Control Process. Planning and implementing the validation tasks will be a part of the role, as well as software and hardware configurations.The role will comprise;-validation of image quality-workflow-patient ergonomics/ comfort-document validation plans-test protocols-FDA guidelines-customer service-cross functional developmentsRequirements:BS/MS in Engineering, Computer Science or equivalent technical degreeExperience in clinical product design validation for Medical device industryExperience in Quality and Regulatory Management SystemThis is an urgent role, please send your resume immediately if you are interested]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[QA Inspectors  North  East  Contract  URGENT]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD993EA5411CC1778482579F5001FD10B</referencenumber>
<City><![CDATA[New Jersey]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/QA-Inspectors-North-East-Contract-URGENT_1651699.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[QA consultancy is seeking a number of QA inspectors for ongoing contractsDescription:and#149;Lead Responsibilities include investigations related to all deviations including process and equipment deviations and deviations in manufacturing. and#149;Responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities:and#149;Have a fundamental understanding of the investigation process as it applies to manufacturing issues and#149;Have detailed understanding of the processes and systems involved in the manufacture of bio pharmaceutical.and#149;Be able to use that knowledge to investigate process deviations and atypical results and identify root cause Requirements and#149;BS or MS in a scientific or engineering discipline with 3+ years. and#149;A strong technical background in a cGMP and Quality environment is required. Prior experience with investigations including conducting and writing investigations preferred. and#149;MOST CRITICAL: Knowledge of the processes used to manufacture biologics and a understanding of Trackwise and practices used to investigate, document and correct atypical events that occur in the process INITIAL 3 MONTH ASSIGNMENT WITH THE POTENTIAL OF BEING EXTENDED UP TO ONE YEAR IN LENGTH. Starting ASAP - this is an URGENT requirment. APPLY NOW and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[LIMS Administrator]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9D5DBD6E690C4A2E482579F5001FD11A</referencenumber>
<City><![CDATA[Washington]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/LIMS-Administrator_1651700.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[A venture-funded biotechnology company is currently recruiting for a LIMS administrator. The goal of the company is to develop a molecular in vitro diagnostic test to interrogate biological circuits contributing to the pathogenesis of Alzheimers disease and lung cancer. The management team is looking for a highly motivated professional who has experience in protein biochemistry, liquid chromatography and sample processing to help establish a CLIA-certified clinical laboratory. Duties:-Implement new system from the ground up, consult with end users about their needs for system implementation-Document detailed requirements based on input from end users.-Perform end-user training, design reports and workflows that meet their needs-Create manuals, SOPS and training documentation-Troubleshoot system errors, design and run test configurations, implement solutions internally or in conjunction with the vendor-Set up, maintaining, and troubleshooting interfaces with analytical instruments-Performing detailed and accurate record keeping compliant with our lab accreditations-Maintain the LIMS configuration and develop and implement new configurations]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Control Contractor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobC85FE11E3D54F707482579F5001FD127</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Control-Contractor_1651701.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Senior Quality Control Contractorand#60;/band#62;and#60;/uand#62;A pharmaceutical company in the South San Francisco area is looking for a Senior Quality Control Contractor to join their team for a 6 month contract.  The Sr. Manager will be managing different projects and needs to be very proactive.and#60;band#62;Senior Quality Control Contractor Requirements:and#60;/band#62;and#149;  Interact with and provide oversight of contract laboratories to coordinate outsourced in-process release and stability testing.and#149;  Compile, review, and approve vendor raw data and COAs for release testing.and#149;  Help to troubleshoot OOS and OOT investigations, and serve as a technical resource for contract laboratoriesand#149;  Being responsible for compilation, review, and data entry/review into the LIMS system for ongoing stability studies.and#149;  Be responsible for the management of stability databases and preparation of in-house reports and stability updates for submissions to regulatory authorities.and#60;band#62;Senior Quality Control (QC) Contractor:and#60;/band#62;and#149;  Contract/consultant backgroundand#149;  8+ years of Quality Control experienceand#149;  Understanding of release testing and stability testingand#149;  Experience working with contract laboratoriesand#149;  Understand the challenges of working of working with a virtual companyand#149; Understands analytical methods and developmentIf you are interested in this role, please reply to this job positing immediately to be considered.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Lead SAS Programmer, Clinical Trials, CDISC, San Diego]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2AC76814DA17EAE0482579F5001FD133</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Lead-SAS-Programmer-Clinical-Trials-CDISC-San-Diego_1651702.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client has a long term contract requirement for a SAS Programmer with CDISC experience based from there offices in San Diego.Responsibilities include:- Serve as Lead on the project level to plan, organize, and manage a team from start to finish by overseeing all development, validation, and production of programs on a project - Manage CRO programming activities for complex studies - Manage project timelines, responsibilities, and deliverables by interfacing with all levels of management to negotiate resources, project priorities and scopes - Provide expert review of process and methodology development work at the highest level with regard to standards and validation procedures - Provide software and programming solutions across projects and/or technologies to meet business needs - Provide input to drug development in the areas of scope, budget, and timelines related to programming activities - Develop, revise, and maintain (SOPs) in conjunction with other departments - Monitor the quality of programs, specifications, and other programming work by ensuring the good programming practices and compliance with all the SOPsQualifications:- Expert knowledge of SAS/clinical trials is required. - Combination of in house and CRO experience preferred. - Knowledge of other software such as S-plus and WinNonlin is preferred. - Knowing the pertinent industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines, is required. This is a fantastic opportunity for a long term contract with a large Pharmaceutical Client.If you meet the criteria then please apply immediately to be considered for an interview.Key Words: SAS, CDISC, S-plusClinical Trials, IVD, Programmer, Biometrics, CDM, Clinical Data Management, Biostatistics, Statistician, San Diego, Project Management, CRO]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Scientist]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB699BF25EB82C474482579F5001FD141</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Clinical-Scientist_1651703.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[As the Clinical Scientist you will be responsible for the design, implementation, analysis, and reporting of studiesconducted within one or more programs. Key Accountabilities will be: Assisting the Senior Clinical Director in the overallmanagement, planning, evaluation, filing and documentation of projects and studiesParticipation in ongoing medicine development activities including:Preparation of regulatory documents and interaction with global regulatory authoritiesReview of incoming data Analysis, presentation and interpenetration of ongoing studies and published dataInteractions with health authorities and expert bodiesClose collaboration with drug safety, regulatory affairs, medical affairs and clinical trial operations Participation in the preparation of abstracts, posters and presentations for scientific meetings and congresses Developing and writing clinical plans and protocols ensuring that they are scientifically sound]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager Quality Control (QC)]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobAD8A4C2E3886252D482579F5001FD14C</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Senior-Manager-Quality-Control-QC_1651704.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[and#60;uand#62;and#60;band#62;Senior Manager, Quality Control (QC)and#60;/band#62;and#60;/uand#62;A pharmaceutical company in the South San Francisco area is looking for a Senior Manager, Quality Control to join their team for a 6 month contract.  The Sr. Manager will be managing different projects and needs to be very proactive.and#60;band#62;Senior Manager Quality Control Responsibilities:and#60;/band#62;and#149;  Interact with and provide oversight of contract laboratories to coordinate outsourced in-process release and stability testing.and#149;  Compile, review, and approve vendor raw data and COAs for release testing.and#149;  Help to troubleshoot OOS and OOT investigations, and serve as a technical resource for contract laboratoriesand#149;  Being responsible for compilation, review, and data entry/review into the LIMS system for ongoing stability studies.and#149;  Be responsible for the management of stability databases and preparation of in-house reports and stability updates for submissions to regulatory authorities.and#60;band#62;Senior Manager, Quality Control (QC) Requirements:and#60;/band#62;and#149;  Contract/consultant backgroundand#149;  8+ years of Quality Control experienceand#149;  Understanding of release testing and stability testingand#149;  Experience working with contract laboratoriesand#149;  Understand the challenges of working of working with a virtual companyand#149; Understands analytical methods and developmentand#60;band#62;If you are interested in this role, please reply to this job positing immediately to be considered.and#60;/band#62;]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[SENIOR ACCOUNT EXECUTIVE  MEDICAL COMMUNICATION AGENCY  CHICAGO]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7A96D1DDAA478CF0482579F5001FD159</referencenumber>
<City><![CDATA[Illinois]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/SENIOR-ACCOUNT-EXECUTIVE-MEDICAL-COMMUNICATION-AGENCY-CHICAGO_1651705.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[SENIOR ACCOUNT EXECUTIVE - MEDICAL COMMUNICATION AGENCY - CHICAGOMy client, located in Chicago, is looking for a Senior Account Executive to join their rapidly growing team. They are offering a very competitive salary, a bonus incentive, and full coverage on Health Benefits.Further, the agency as a whole has doubled in size and revenue for the past 3  years (year over year). They diversify their accounts and therapeutic areas, which has been key to the success of the agency.DAY TO DAY:+ Agency experience in a medical communication, pharma, or advertising agency + Key, day-to-day representative to the client+ Manages client feedback and disseminates to the internal team+ Liaises with strategic personnel to ensure the proper strategic brand imperatives are met beyond a tactic+ Remains accountable for deliverables sent to the client+ Manages execution of tactical plans+ Develops and manages budgets, timelines and proposals+ Develop agendas for client meetings+ Communicates timelines and tasks to various internal departmentsIf interested, upload resumes directly or call Brian Barranti on (212) 707-8499 for more information.SENIOR ACCOUNT EXECUTIVE - MEDICAL COMMUNICATION AGENCY - CHICAGO]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[GCP Auditor]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD87CF277615C81DB482579F5001FD167</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/GCP-Auditor_1651707.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[The Senior Auditor/Manager, QA GCP will be responsible for assisting the Senior Director in implementing GCP Quality Assurance programs for the conduct of clinical trials, including conducting and reporting internal/external audits, clinical study reports and other documents; providing compliance advice to clinical project teams and assisting with other departmental needs.The company is currently focused on three programs in late stage clinical development, targeting large, unmet medical needs. Dimebon is in a global Phase 3 trial in Alzheimerand#146;s disease.  The companyand#146;s second compound, MDV3100 is in two global Phase 3 trials in castration-resistant prostate cancer.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer  Medical Device]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4196A4FD2A737DD9482579F5001FD174</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Quality-Engineer-Medical-Device_1651708.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffings Medical Device client in Sunnyvale, CA, requires a Quality Engineer for a contract to hire position. Responsibilities: and#149; Implement quality system in accordance with cGMP and ISO standards and#149; Oversee all aspects of the product/process validation program, including IQ/OQ/PQ protocols, monitoring, and preparation of reports. and#149; Lead quality assurance tasks in development and manufacturing to ensure processes are capable and quality tools and systems are in place through product life cycle. and#149; Lead investigative teams to determine root causes of quality issues. and#149;Support resolution of CAPAs to solve production/quality issues. Qualifications: Education: BS / MS in Mechanical Engineering, Chemical Engineering, or related discipline. Training in quality engineering and procedures. Experience and#38; Skills: and#149; 5 or more years in a quality engineering role in the combination product / medical device industry. Specific experience with drug-eluting stents is a big plus. and#149; Solid knowledge of current Good Manufacturing Practices (cGMP) and ISO standards for both pharmaceuticals and medical devices. and#149; Proficiency in equipment and process validation methods and#149; Hands-on experience with statistical methods of analysis. and#149; Effective communication and interpersonal skills, including technical report writing and presentations.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Bioinformatics Systems Administrator]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob4C10240BF6656690482579F5001FD180</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Bioinformatics-Systems-Administrator_1651709.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Global Biotechnology Company is seeking to bring on a systems administrator to their Bioinformatics Team.  This is a long-term contract position and only local candidates will be considered for this role.  Requirements:- Work with customers and internal development teams to troubleshoot and resolve IT-related issues including Linux clusters and software related to data analysis. - Work with customers to solve IT and bioinformatics challenges, including troubleshooting, problem-solving, scripting work to resolve issues. - Masters degree in Information Technology, Information Technology Systems Administration or High Performance Computing plus 3 years experience in position offered or as Software Developer or Systems Analyst. - Must have demonstrated experience or knowledge of UNIX/Linux administration; computing environment in next generation sequencing; designing, building and maintaining high-performance computing clusters and storage; cluster management software (such as Rocks and#38; Scyld) and resource managers and job schedulers (such as PBS, Torque, LSF, SGE and#38; Maui); C, C++, PERL, Python, Java and shell scripting; GPFS, Lustre, GlusterFS filesystems; Nagios and Ganglia tools; and Cluster Management software such as Xcat, Perceus, or PBS P]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Sr Quality Engineer Medical Device]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobF107C30DF211C6E2482579F5001FD18B</referencenumber>
<City><![CDATA[California]]></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineerjob.us/job/Sr-Quality-Engineer-Medical-Device_1651710.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Real Staffing Group is currently looking for a Sr Quality Engineer to join a fantastic medical device company in the Mountain View Area.Role: As the Sr QE, you are responsible for performing all quality tasks for NPD, supplier management, complaint analysis, root-cause analysis, and corrective action for this companyand#146;s Class II device. You will be managing your own work load and interacting with cross-functional teams on a daily basis. Requirements:BS Degree in Engineering or Life Science 3+ yrs of Quality Engineering experience within medical device or highly regulated environmentPassionate and Motivated individual who wants to influence others and build team relationshipsSalary80-110k based on experienceYou: If you are interested in working for a well know company that prides themselves on producing quality medical devices in a competitive industry, then please send me your updated resume and I will follow-up with you. Thank you.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager Regulatory Affairs Stelle]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobE08DF9725FCC703F482579F5001FD196</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Manager-Regulatory-Affairs-Stelle_1651711.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde aus Bayern ist ein weltweit agierendes Pharmaunternehmen, das viele sehr innovative Medikamente herstellt. Im Moment wird dringlich ein erfahrender Senior Regulatory Affairs Manager gesucht, der Lust hat sich um europand#228;ische Zulassungen zu kand#252;mmern.Wollen Sie mit internationalen Entwicklungsteams arbeiten? Und mit der EMA, nationalen europand#228;ischen Behand#246;rden in Kontakt zu sein? Weitere Aufgaben:-CTAs, MAAs, Variations, Amendments, und Renewals-MRP and#38; DCP-Gap Analysis fand#252;r Clinical/Technical DokumentationWas sollten Sie mitbringen?Ein abgeschlossenes Pharmazie- oder Naturwissenschaftliches Studium, Berufserfahrung im europand#228;ischen Regulatory Affairs Umfeld mit Focus  auf Drug Development, Clinical Trial Applications und European Marketing Authorization sowie Centralised Approval Procedures. Erfahrungen aus dem Onkologie-Bereich wand#228;ren vorteilhaft. Gute Englischkenntnisse sind ein Muand#223;, Deutschkenntnisse wand#228;ren von Vorteil. Bei weiteren Fragen kontaktieren Sie, Frank Seipel (Real Pharma Frankfurt) unter 069 264 89 8400 oder senden Sie direkt mir Ihre vollstand#228;ndigen Bewerbungsunterlagen.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Vice President Corporate Regulatory Affairs]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob232AAA591992394D482579F5001FD1A2</referencenumber>
<City><![CDATA[Rheinland]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Vice-President-Corporate-Regulatory-Affairs_1651712.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client is the worlds largest fragrance company. They have a diverse product portfolio of different very famous beauty products (cosmetics, toiletries, skin care, etc.). At the moment they are looking for a new Vice President Corporate Regulatory Affairs guarantee a strong Regulatory Affairs process to support company business growth as well as to ensure compliance of regulatory requirements globally.Further you will do effective monitoring to detect emerging regulatory developments, and represent the organization at national/international associations (active membership). You will be leading a multinational team across countries (team of 7 as direct reports based in Germany), support all company brands on regulatory issues. If you a role model who talks the talk and walks the walk, donand#146;t wait and apply now. You skill set:-Scientific education, Ph.D on Pharma, Chemistry -Strong experience with worldwide Registrations-Strong leadership on international, multinational team-Fluency in English, plus good command of German   For further information about this great opportunity, please e-mail or call Frank Seipel (Senior Regulatory Affairs Recruitment Consultant) at Real Pharma on 0049 (0) 69 26 489 8400.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs CMC in MITTELHESSEN]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9DD790805D965A42482579F5001FD1AE</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-CMC-in-MITTELHESSEN_1651713.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[My client specializes in the treatment of strong pain and supplies medicines for substitution and tumour treatment, as well as antiseptics and wound treatment. At the moment they are looking for a REGULATORY AFFAIRS MANAGER CMC. Do you want to work internationally in areas such as the EU, Asia-Pacific, and Latin America?Your responsibilities will be project management for regulatory submissions, renewals and variations. In addition to that you will be giving regulatory and scientific guidance to the project teams for all CMC related questions. Supporting internal and#38; external compliance through critical assessment of CMC documentation and GMP processes will also be part of your job spec.Do you want to work cross functionally to design, initiate and deliver on-time projects and compliance initiatives throughout the business?What you need to bring along:Scientific degree, experience in Regulatory Affairs (Preferred working  experience in areas of Rand#38;D, QC or operational pharmaceutical departments) as well as strong experience in International regulatory procedures and requirements (EU, Asia-Pacific, Latin America). Understanding of both English and German languages is a must.For further information about this great opportunity, please e-mail or call Frank Seipel (Senior Regulatory Affairs Recruitment Consultant) at Real Pharma on 0049 (0) 69 26 489 8400.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Softwareentwickler]]></title>
<date>Sat, 05 May 2012 00:00:00 GMT</date>
<Closedate>Wed, 04 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob61C7FF8319A43A33482579F5001FD1BA</referencenumber>
<City><![CDATA[Baden]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Softwareentwickler_1651714.html</url>
<company><![CDATA[Progressive Recruitment]]></company>
<description><![CDATA[Mein Kunde ist in der Medizintechnik. Das Unternehmen befindet sich in Baden-Wand#252;rttemberg. Ab sofort suche ich einen Softwareentwickler.SoftwareentwicklerAufgaben:Neu- und Weiterentwicklung der Software fand#252;r  medizinisch-diagnostische Messergebnisse.Anhand von C#, WCF, WPF, analysieren, designen und realsieren komplexe Softwaresysteme. Sie sind ebenfalls fand#252;r die bjektorientiere Entwicklung zustand#228;ndig mit agilen Methoden in C# und C++.ProfilStudium der (technischen) Informatik, o.v.Berufserfahrung in der Programmierung von C#, C++, WCF und WPF.Erfahrung in Visual Studio ist von Vorteil.Sie benand#246;tigen sehr gute DeutschkenntnisseAgile Softwareentwicklung ist sehr von VorteilSie erwartet eine and#228;uand#223;erst leistungsgerechte Vergand#252;tung und ein global agierendes Unternehmen. Bewerben Sie sich jetzt als SoftwareentwicklerSenden Sie mir Ihren CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs Manager in Baden  Württemberg gesucht]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobB33CCF8E8BCD1903482579F600222479</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Wrttemberg]]></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-Manager-in-Baden-and-amp-SHARP150-W-and-amp-SHARP252rttemberg-gesucht_1640166.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Aktuell suche ich fand#252;r ein mittelstand#228;ndisches, international tand#228;tiges Unternehmen der Medizintechnik einen Manager im Bereich Regulatory Affairs. Gesucht werden sowohl Mitarbeiter mit einschland#228;giger Berufserfahrung als auch Berufseinsteiger mit ersten Erfahrungen aus diesem Bereich.Zu Ihren Aufgaben gehand#246;rt die Planung, Durchfand#252;hrung und Betreuung von Zulassungsprozessen sowie die Erstellung der relevanten Dokumente. Sie werden verantwortlich fand#252;r die Koordination und Einhaltung der notwendigen nationalen und internationalen Regularien sein, und darand#252;ber hinaus Ansprechpartner fand#252;r jegliche Fragen aus diesem Bereich sein. Des Weiteren gehand#246;rt auch die and#220;berprand#252;fung der Vertriebsfand#228;higkeit der Produkte zu Ihren Aufgaben.Idealerweise haben Sie ein technisches Studium erfolgreich abgeschlossen, und bereits erste Erfahrungen in der praktischen Umsetzung und Pflege von Zulassungen gesammelt. Zu Ihren Qualifikationen zand#228;hlen sehr gute Englischkenntnisse sowie gute MS-Office-Kenntnisse. Ihr Profil wird durch Ihre Kommunikationsstand#228;rke, Durchsetzungsvermand#246;gen und Ihre Teamfand#228;higkeit abgerundet.Habe ich Ihr Interesse geweckt? Dann zand#246;gern Sie nicht, und kontaktieren mich!Gerne erhalten Sie fachlich kompetent und diskret weitere Informationen.Ihre Ansprechpartnerin ist:Alexandra GeorgopoulosTel. 069 264 89 8400a.georgopoulos(a)realstaffing.comIch freue mich auf Ihren Lebenslauf als Word-Format und and#252;ber einen Besuch auf meinem Xing-Profil. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior QA Manager (Engineering)  Illinois]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob51A9ADB294FE84C2482579F600222489</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-QA-Manager-Engineering-Illinois_1640178.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Senior QA Manager (Engineering) - IllinoisSUMMARYMy client are looking for a Senior QA Manager with an Engineering background.The Senior Manager Quality Engineering at Libertyville, IL is responsible for managing a team of Quality Engineering professionals and for providing guidance on the application of Design Controls for project teams based at the Libertyville facility.  The Senior Manager provides guidance on the application of Quality and Reliability Engineering methods to groups and project teams at all facilities. RESPONSIBILITIESProvide guidance to corporate project teams with the application of Design ControlsLead Risk Analysis activities for evaluation of the product design.and#149;Facilitate the Risk Assessment meeting to evaluate the safety of a product design or design change, and to determine methods to eliminate or mitigate hazards.and#149;Document results.Work with NPD, Rand#38;D, and/or TSG on product design verification and validation activities.and#149;Participate in the development of the Traceability Matrix, which includes the product design Verification and Validation Plans.Work with the Plant QA managers to coordinate Plant Quality Engineering activities with corporate quality strategiesand#149;Communicates with QA managers regarding corporate QE strategies.and#149;Negotiates needed resubmissions or adjustments to documentation with plant and corporate management.Manages preproduction and first article processes at the corporate headquarters for evaluation, approval, and maintenance of recordsand#149;For First Articles, and for Preproductions that are not fully approved at the plant level:and#149;Coordinate evaluation process with required departments.Negotiates needed resubmissions or adjustments to documentation with plant and corporate management.Change/Work Request Systemand#149;When assigned and appropriate, review C/WRs and provide guidance on necessary deliverables.and#149;Collaborate with the C/WR project leader regarding any required test plans, experimental design, evaluation of data.and#149;Participate in the design control process, if required.and#149;Interface with the plants (QM, QE) to ensure plant perspective and requirements are taken into account.Product drawing evaluation and approvaland#149;Evaluate design to determine requirements for QA check points.and#149;Evaluate documentation for correctness.and#149;Alternate for product specification and ECN approval panels in QUMAS.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Manager of Quality Engineering  Medical Devices]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob86C734248158C99A482579F6002224A1</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Manager-of-Quality-Engineering-Medical-Devices_1640179.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Senior Manager Quality EngineeringSUMMARYThe Senior Manager Quality Engineering at Libertyville, IL is responsible for managing a team of Quality Engineering professionals and for providing guidance on the application of Design Controls for project teams based at the Libertyville facility.  The Senior Manager provides guidance on the application of Quality and Reliability Engineering methods to groups and project teams at all facilities. QUALIFICATIONSAcademic/Credentials/Certifications:B.S. Degree in Engineering or other related technical fieldLength of Experience:and#149;Minimum of 10 years of experience in supervision (management of quality engineering associates required)and#149;Minimum of 10 years in the quality fieldand#149;Minimum of 10 years in the medical products industry (medical device industry preferred)Specialized Skills/Technical Knowledge:ASQ Certified Quality EngineerASQ Certified Reliability EngineerKnowledge of applicable standards and regulations:- cGMP/21CFR820- EU MDD 93/42/EEC- ISO 14971- ISO 13485: 2003Ability to read and interpret product drawings and to set up and perform statistical and dimensional analyses.Preferred:MS in Technical Management, Statistics, or MBALicensed PEExperience in statistics, instrumentation, molding, electronicsAdvanced QA coursesExperience with electronic medical devicesExperience with plastics, films, and moldingOther Certifications:- Certified Quality Manager- Certified Software Quality Engineerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer  Medical Devices]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobDBF1A8E92258A28F482579F6002224AD</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Engineer-Medical-Devices_1640180.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[One of my clients, a world renown Medical Device company based in Libertyville, Chicago are looking for a Senior Quality Engineer to join their company. The Senior Quality Engineer will need to have a strong background in QA as well as a good education and will also have excellent communication skills. QUALIFICATIONS  Academic/Credentials/CertificationsB.S. Degree in Engineering or Engineering in Technology, or equivalent Length of experienceMinimum two years as a Quality Engineer in addition to four years industry experience in a quality related field. Specialized skills/technical knowledgeLaboratory expirenceAble to read and interpret product drawingsAble to set-up and perform dimensional analysisand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Engineer]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob02D52BE08E586653482579F6002224BD</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Quality-Engineer_1640181.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Quality Assurance Engineer supports new product development in Raw Material selection and qualification. Global cost saving projects on new Raw Materials and Global projects on harmonisation across plants on quality standards within own responsibility arear.The Quality Engineer is involved in vendor evaluation, qualification and performance as well as optimizing Raw materials Performance and Quality.Optimize current laboratory rutines, incomming inspection and Test methods in the QA lab. RESPONSIBILTIESSupport New Product Development (Raw Materials):   50%a) Represent Quality Management on product development teams (Raw Materials)b) Ensure that quality and reliability in current Test Methods and implementation of new  Test Methods in QA Laboratory. c)  Ensure that documentation is updated and new procedures implemented.d)  Coordinate raw materials inspection documents and training with the Raw Material Teame)  Assist with 0-series and +1 series review.f)  REACH and#150; update corporate document. Global projects and cost saving initiatives:   20%a) Review new CWR on new mateials for safety/ tox, efficacy, and reliability issues.b) Review the plan and results for new material qualification.Optimize Existing Raw Material Quality:   20%a) Provide material performance analysis based on Production input and venror performanceb) Perform internal audits and help to continuously improve the quality system.Vendor Evaluation and Performance:   10%a) Interface with other corporate departments and the plants to develop new potential vendors and assure their acceptabilityb) Participate in resolving specification questions leading to acceptance of Hollister specifications by vendorsc) Identify and communicate to the involved corporate departments information about the performance of existing vendors.  Recommend any necessary corrective actions.d)  Perform audits of potential and existing vendors, and rate their level of acceptability.If you want to apply - send over your resume today.and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Software Entwickler Medizintechnik Hamburg Sofort zu besetzen]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob72FB0A7039C8FACE482579F6002224D7</referencenumber>
<City><![CDATA[Hamburg]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Software-Entwickler-Medizintechnik-Hamburg-Sofort-zu-besetzen_1640199.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Mein Kunde ist in Norddeutschland und in der Medizintechnik ansand#228;ssig. Das Unternehmen ist global tand#228;tig und bereits auf eine sehr langen Firmengeschichte zurand#252;ckgreifen. Aufgrund der stetigen Nachfrage nach deren Produkten, benand#246;tigt mein Kunde fand#252;r den schnellstmand#246;glichen Zeitpunkt einen Software Entwickler.Software-EntwicklerIhre Aufgaben:Sie sind fand#252;r Kleinprojekte verantwortlichSie betreuen zusand#228;tzlich externe DienstleisterEntwicklung von Computer-Softwareland#246;sungen C/C++ and#38; C# fand#252;r die MedizintechnikVerantwortlich fand#252;r Modul- und Test-StrategieErstellung von SpezifikationenIhr Profil:Studium der Informatik o. and#228;. Erfahrung in C/C++Erfahrung in C# und .NET Sie sollten ebenfalls Kenntnisse in grafischen Benutzeroberfland#228;chen besitzen sowie in SQL- DatenbankenBerufserfahrung ist wesentlich von VorteilSie mand#246;chten in einem Traditionsunternehmen neu Fuand#223; fassen? Sie wand#252;nschen sich Respekt und Anerkennung?Dann bewerben Sie sich jetzt als Software Entwickler!Schicken Sie mir umgehend Ihr CV im WORD Format max. 1MB, and#252;ber den Online Bewerbungslink oder an:j.santos(at)realstaffing.comJoel Santos, Tel.: 069 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance Clinical Trial Assistant  Bayern  1.0 FTE]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0CF5D452D03399DE482579F6002224E6</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-Clinical-Trial-Assistant-and-amp-SHARP150-Bayern-10-FTE_1640216.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[My client is an international specialty Pharma Company in the heart of Bayern with a truly great environment to work in. They are currently seeking a Freelance Clinical Trial Assistant for 6 months+. The role offers a great opportunity for those who may be looking for a new challenge in life. You should also have a very strong interpersonal skills and good experience in the Clinical Research area. Also excellent organizational and time management skills are required. Key Responsibilities:and#149;Is responsible for writing Agenda and#38; Minutes and#149;Support in organization of meetings and#149;Assists in the coordination of activities to ensure CRO and vendor delivery against the contracted scope of   work and#149;Provide practical support to the Clinical Operations group in the set up of the administration for the management of Clinical Trials and#149;Filing/archiving of documents in-house in line with GRT SOPand#146;s in close operation with the Clinical Trial Documentation and Archiving Unit and#149;Assist in ensuring that trial related documentation is accurate and up to date and#149;Assist in ordering trial related material and#149;Is responsible for tracking of all trial related information (e.g. CTMS)  Expertise and Complexity:and#149;Clinical experience preferredand#149;Excellent organizational and time management skillsand#149;Ability to keep detailed and accurate recordsand#149;Very strong interpersonal skills, flexibilitySalary/ Duration:and#149;Negotiableand#149;Start 01.06.2012and#149;End  01.12.2012 (with option on extension)As a specialist recruiter in Clinical Research positions for Pharmaceutical clients in Germany and Switzerland, this is one of many current vacancies I have for my clients in various locations. Therefore even if this position is not of interest to you please do not hesitate to contact me as there may be other roles that are currently not advertised that you may be interested in.Apply now! Call Parminder Singh at +49 69 264 89 8400 and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Quality Engineer  Medical Devices]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7ECDF2FF4FD7A480482579F6002224F9</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago]]></State>
<url>http://www.engineerjob.us/job/Senior-Quality-Engineer-Medical-Devices_1651796.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[One of my clients, a world renown Medical Device company based in Libertyville, Chicago are looking for a Senior Quality Engineer to join their company. The Senior Quality Engineer will need to have a strong background in QA as well as a good education and will also have excellent communication skills. QUALIFICATIONS  Academic/Credentials/CertificationsB.S. Degree in Engineering or Engineering in Technology, or equivalent Length of experienceMinimum two years as a Quality Engineer in addition to four years industry experience in a quality related field. Specialized skills/technical knowledgeLaboratory expirenceAble to read and interpret product drawingsAble to set-up and perform dimensional analysisand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Statistiker mit Karrierechancen]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob290D50496F7EDF11482579F60022250C</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Statistiker-mit-Karrierechancen_1658775.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Mand#246;chten Sie tagtand#228;glich Ihr Bestes geben und daneben Ihre Karriere vorantreiben indem Sie immer mehr dazulernen und dies von den Besten auf Ihren Gebiet? Dann ist diese Stelle genau das Richtige fand#252;r Sie!Das Unternehmen zand#228;hlt zu den grand#246;and#223;ten Arbeitgebern auf ihrem Bereich in der Region Basel und beschand#228;ftigt rund 5.000 Mitarbeiter. Mit dem Ziel tagtand#228;glich ihr Bestes zu geben setzt sich mein Kunde hohe Ziele um die Lebensqualitand#228;t tausender Patienten zu verbessern. Um die hohe Qualitand#228;t zu gewand#228;hrleisten setzt das Unternehmen vor allem auf seine Mitarbeiter in die sie sehr viel investieren. Von Mentorenprogrammen and#252;ber Coaching, sei es intern oder extern, wird sichergestellt, dass die Mitarbeiter den Patienten die bestmand#246;gliche Versorgung bieten kand#246;nnen.Um auch in Zukunft die hohe Qualitand#228;t bieten zu kand#246;nnen und die wachsenden Patientenzahl  behandeln zu kand#246;nnen sucht mein Kunde einen Senior Statistiker um das Epidemiologie und Statistiker Team zu unterstand#252;tzen.Das Unternehmen sucht einen Bewerber / eine Bewerberin mit einem Abgeschlossenen Medizinstudium oder einem Studium im verwandten Bereich. Weiterhin sind einige Jahre Erfahrung wand#252;nschenswert. Daneben sollten Sie sicher im Umgang mit SAS und / oder R sein und bereits erste Erfahrung mit der Fand#252;hrung von Teams gesammelt haben. Der richtige Bewerber ist weiterhin flieand#223;end in Englisch und kann sowohl Artikel auf Englisch verfassen als auch die Studienresultate auf Englisch prand#228;sentieren. Deutsch wand#228;re von Vorteil.  Mein Kunde bietet Ihnen ein sehr internationals Arbeitsumfeld in einem sehr internationalen Team. Das Team besteht momentan aus 3 Statistikern in einer Abteilung in der 20 Mitarbeiter arbeiten. Daneben bietet das Unternehmen sehr gute Karrieremand#246;glichkeiten, sowie stetige Weiterbildungen. Sei es internes und / oder externes Coaching oder Mentorenprogramme and#150; Bei diesem Unternehmen lernen Sie von den Besten auf Ihren Gebiet. Ich arbeite als Recruitment Consultant fand#252;r Real Pharma und bin fand#252;r den Bereich Biometrik und HEOR innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 435080972 zu erreichen. Ansonsten kand#246;nnen Sie mich auch gerne unter k.schirmer(at)realstaffing.com kontaktieren. Keywords: Epidemiologie, Epidemiology, Suisse, Schweiz, Switzerland, German, English, Deutsch, Englisch, Life Science, Basel, Biostat, Biostatistik, Biostatistician, Statistician, Klinische Forschung, clinical study, klinische Studie, Qualitand#228;t, Healthcare, Patienten, Patients, Karriere, Basel Stadt, BS, Basel Land, BLand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Global Business Intelligence Analyst  Hull  Circa. £40K]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob66A09A86D018971C482579F600222528</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Global-Business-Intelligence-Analyst-Hull-Circa-and-amp-SHARP16340K_1640326.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[and#60;band#62;Global Business Intelligence and#150; Hull and#150; Major Healthcare Company  and#60;/band#62;The GBI team is responsible for strategic intelligence support and competitor intelligence provided primarily to Group staff, covering all of the major OTC categories. and#60;band#62;Scope of Roleand#60;/band#62; The role interfaces with all parts of the organisation  and#150; both inward-facing in its focus on  own brands and outward focused in tracking competitor / industry activity. The BI function, and outputs of their analysis, acts as an early warning system of competitor and industry activity, highlighting potential opportunities and threats. Learningand#146;s, conclusions and findings often input to key changes in RB processes, organisation and strategy.and#60;band#62;Responsibilitiesand#60;/band#62; Project-based research and analysis: Undertake a wide range of project-based requests from senior management. These can vary in length, subject and level of analysis required, but typically involve accessing different sources, validating and challenging data; delivering the output/conclusion in presentation formatTracking and reporting competitor innovation and key activitiesStrategic Planning: Work on internally focused projects such as Portfolio Analysis, forecasting opportunity sizes and assessing potential of new geographies.Benchmarking: Analyse key financials for competitive set and report regularly on performance. and#60;band#62;Experienceand#60;/band#62;Honours Degree  - either: 2 / 3 years experience in OTC Healthcare / Pharmaceuticals and#150; within a business / competitor / intelligence function OR consulting OR Strategic Planning.Experience of working within (or adjacent to) an international marketing environment would be useful. and#60;band#62;Skillsand#60;/band#62;and#149; Excellent analytical skills and#150; ability to scope and structure complex data and present and visualise the findings and conclusions at a strategic level.and#149; Ability to work with unstructured information from a wide variety of sources and synthesise in a highly summarised strategic format.and#149; Experience in working with and analysing large data sets is essential and#150; previous modelling, statistical analysis project would be useful.and#149; High level Excel skillsand#149; Familiarity with key elements of company Pand#38;Ls and financial ratios.and#149; Ability to manage and prioritise the ongoing monitoring / tracking activities required within GBI vs project demands.For further information contact Sarra Gwilym on 0207 758 7311 or forward your CV for direct application.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Statistiker mit Karrierechancen]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob31C82969FF19B82C482579F60022253C</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Senior-Statistiker-mit-Karrierechancen_1640379.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Mand#246;chten Sie tagtand#228;glich Ihr Bestes geben und daneben Ihre Karriere vorantreiben indem Sie immer mehr dazulernen und dies von den Besten auf Ihren Gebiet? Dann ist diese Stelle genau das Richtige fand#252;r Sie!Das Unternehmen zand#228;hlt zu den grand#246;and#223;ten Arbeitgebern auf ihrem Bereich in der Region Basel und beschand#228;ftigt rund 5.000 Mitarbeiter. Mit dem Ziel tagtand#228;glich ihr Bestes zu geben setzt sich mein Kunde hohe Ziele um die Lebensqualitand#228;t tausender Patienten zu verbessern. Um die hohe Qualitand#228;t zu gewand#228;hrleisten setzt das Unternehmen vor allem auf seine Mitarbeiter in die sie sehr viel investieren. Von Mentorenprogrammen and#252;ber Coaching, sei es intern oder extern, wird sichergestellt, dass die Mitarbeiter den Patienten die bestmand#246;gliche Versorgung bieten kand#246;nnen.Um auch in Zukunft die hohe Qualitand#228;t bieten zu kand#246;nnen und die wachsenden Patientenzahl  behandeln zu kand#246;nnen sucht mein Kunde einen Senior Statistiker um das Epidemiologie und Statistiker Team zu unterstand#252;tzen.Das Unternehmen sucht einen Bewerber / eine Bewerberin mit einem Abgeschlossenen Medizinstudium oder einem Studium im verwandten Bereich. Weiterhin sind einige Jahre Erfahrung wand#252;nschenswert. Daneben sollten Sie sicher im Umgang mit SAS und / oder R sein und bereits erste Erfahrung mit der Fand#252;hrung von Teams gesammelt haben. Der richtige Bewerber ist weiterhin flieand#223;end in Englisch und kann sowohl Artikel auf Englisch verfassen als auch die Studienresultate auf Englisch prand#228;sentieren. Deutsch wand#228;re von Vorteil.  Mein Kunde bietet Ihnen ein sehr internationals Arbeitsumfeld in einem sehr internationalen Team. Das Team besteht momentan aus 3 Statistikern in einer Abteilung in der 20 Mitarbeiter arbeiten. Daneben bietet das Unternehmen sehr gute Karrieremand#246;glichkeiten, sowie stetige Weiterbildungen. Sei es internes und / oder externes Coaching oder Mentorenprogramme and#150; Bei diesem Unternehmen lernen Sie von den Besten auf Ihren Gebiet. Ich arbeite als Recruitment Consultant fand#252;r Real Pharma und bin fand#252;r den Bereich Biometrik und HEOR innerhalb der Schweiz verantwortlich. Wenn Sie diese Stelle, oder andere Stellen interessieren, bin ich unter der Telefonnummer +41 435080972 zu erreichen. Ansonsten kand#246;nnen Sie mich auch gerne unter k.schirmer(at)realstaffing.com kontaktieren. Keywords: Epidemiologie, Epidemiology, Suisse, Schweiz, Switzerland, German, English, Deutsch, Englisch, Life Science, Basel, Biostat, Biostatistik, Biostatistician, Statistician, Klinische Forschung, clinical study, klinische Studie, Qualitand#228;t, Healthcare, Patienten, Patients, Karriere, Basel Stadt, BS, Basel Land, BLand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Regulatory Affairs  North  £65k  Medical Devices]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob23E6D43A85B22CEC482579F60022254C</referencenumber>
<City><![CDATA[England]]></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Regulatory-Affairs-North-and-amp-SHARP16365k-Medical-Devices_1640407.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Main tasks (primary responsibilities) of the position: Direct and prepare regulatory submissions as required for global approvals for IVDand#146;s, including preparation of reports and interaction with regulatory officials as required Manage  a highly effective Regulatory Affairs function, with line management responsibility for Senior Managers Review product labeling and promotional literature for regulatory compliance Research and interpret regulations, guidelines and precedents to support interdepartmental project teams in developing strategies, policies and procedures that ensure regulatory compliance with global regulatory agencies  Interface with regulatory agencies for inquiries and issues Review Rand#38;D protocols and technical reports and other company documents (including labeling and marketing materials, when applicable) for use in regulatory submissions and in response to queries from regulatory authorities Oversee and direct the preparation of regulatory documentation for country-specific registrations Develop regulatory process SOPs relevant for registration of IVD products or other regulatory aspectsPosition requirements, qualifications and experiences: Extensive experience in the medical device industry, preferably with IVD experience, and extensive regulatory experience, preferably in the area of IVDs, including the preparation and submission of 510(k), PMAs, PLAs, ELAs, IND, IDE, CE Design Dossiers, CE Technical Files, and CLIA Certificate applications.   A proven ability to lead and influence colleagues successfully in a dynamic and evolving matrix environment. Possess a working knowledge of the MDD and IVDD, applicable ISO standards, and US medical device/IVD regulation.   Demonstrated organisational, planning and prioritising abilities, as well as strong technical writing ability;  Must be able to exercise sound judgment for high-level decision-making responsibilities]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Clinical Data Manager  Contract  Pharmaceutical  Illinois]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA07CEE2BAA84B645482579F600222805</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[Chicago North]]></State>
<url>http://www.engineerjob.us/job/Clinical-Data-Manager-Contract-Pharmaceutical-Illinois_1640205.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[My client, a leading Contract Research Organization based in Illinois, now has a fantastic opportunity for Clinical Data Manager to work on a variety of projects across Oncology, CNS and Cardio within Phases II and III.  This is a 12 month contract paying and65 - and70 per hour.The market leading CRO is seeking to hire a talented Clinical Data Manager to work on the full lifecycle of the data management aspect of Clinical Trials within Phases II and III.  This will involve assisting with the creation of the SAP and data plans through to the Database Lock phase.Candidates for this position must have the following skills and experience:- Bachelors degree or higher within Computer Science or related field- 3+ years Data Management experience within Pharmaceutical Medical Device Companies- Proven track record in query creation and resolution- Database Lock experienceApply now for immediate consideration or contact Tom Bakker on 312-453-9088. and#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Produktmanager   Pharma  BadenWürttemberg  ab sofort zu besetzen!]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob7389F4B55466B005482579F60022282B</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Wrttemberg]]></State>
<url>http://www.engineer-job.eu/job/Produktmanager-and-amp-SHARP150-Pharma-and-amp-SHARP150-Baden-W-and-amp-SHARP252rttemberg-and-amp-SHARP150-ab-sofort-zu-besetzen_1640209.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Mand#246;chten Sie in einem mittelstand#228;ndischen Unternehmen beschand#228;ftigt sein, indem and#188; des Umsatzes in Forschung und Entwicklung investiert wird? Mein Kunde ist mit seiner Produktpalette in mehr als 15 Land#228;ndern der Welt prand#228;sent und konzentriert sich auf Produkte u.a. aus dem Bereich der Onkologie.Sind Sie bereit, mit Ihrem Wissen, Ihrer Erfahrung und Ihrer Persand#246;nlichkeit den Firmenerfolg voranzutreiben und Teil eines familiand#228;ren Teams zu sein?Dann sollten Sie als Produktmanager im Pharmabereich Interesse haben.Idealerweise erfand#252;llen Sie als interessierter Kandidat folgende Kriterien:and#149; abgeschlossenes Studium der BWL oder der Naturwissenschaftenand#149; sehr gute Marketing-Kenntnisse, vor allem im strategischen Marketingand#149; Erfahrung innerhalb der Pharmaindustrieand#149; idealerweise haben Sie Ihre Industriekenntnisse im Bereich der Onkologie bzw.   Intensivmedizin gesammeltand#149; verhandlungssicheres Englischand#149; ReisebereitschaftBewerben Sie sich noch heute und warten nicht zu lange. Denn es gibt hier nur eine Stelle zu besetzen. Bei Fragen kand#246;nnen Sie sich an Herrn Elyas Bozan wenden. Wir freuen uns auf Sie.Elyas Bozan, Real Staffing Group  Pharma Division Tel.: +49 (0) 69 264 89 8400 E-Mail: e.bozan(at)realstaffing.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Senior Medical Information Officer  £45k  Benefits, Berkshire]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob100AA3602BC14C6B482579F60022283C</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Senior-Medical-Information-Officer-and-amp-SHARP16345k-Benefits-Berkshire_1651750.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[My client has an outstanding reputation and is a leader in its field. With its vast product portfolio and exciting pipeline, Medical Information is a key focus area.I am looking for someone of strong medical information experience to join a team with great cohesion, motivation and work ethic. Stability, training and excellent benefits are on offer to the right candidate.- Life Science degree - Good working knowledge of the Code of Practice (ABPI)- Copy approval experience preferably on zinc- Excellent oral and written English - To have been involved with delivering training to internal staff and understand the needs of the Field Force- To be able to handle telephone and written enquiriesThis is a varied role with the opportunity to be involved across the board for medical information depending on experience. If you feel you suit the vacancy please send an updated CV to Taran - t.jefferson(a)real-pharma.com]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Associate Director for Market Access urgent required]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob676D19697D03827F482579F60022284E</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Associate-Director-for-Market-Access-urgent-required_1658791.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[With all the healthcare companies focusing on Switzerland companies in this industry are facing high competition. In this competitive world of healthcare sales it is important to have an excellent market access strategy. I am currently searching for one of my clients, a big, international health care company, a Market Access specialist with an international focus. I am searching for individuals with experience in market access in Switzerland and who are fluent in English and German, to be fluent in French would be an advantage. The company is offering you a position in a global, broad based health care company in an international team located in the German speaking part of Switzerland. Working for this company means that you will be working for a company which is recognised as a good place to work and which received numerous local, national and international distinctions. As the Market Access specialist you will act as an area leadership member regarding market access subjects and you would contribute to the area strategy and tactic plans. Additionally this position is responsible for identifying and developing payer solutions to establish and strengthen the portfolio proposition with target payer customers. This position is a strategic and new role which is responsible for setting the new course to create payer customer specific value.   I am a recruitment consultant working in Switzerland. I am specialised in HEOR, Market Access and Biometrics. If you want to get further information regarding this positions, or on many more like this, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com. I am looking forward to receiving your current CV as a word document.  Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, good place to work, international, pricingand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[International Market Access Manager]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob0BABF13658DA5BA7482579F60022285E</referencenumber>
<City><![CDATA[Basel]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/International-Market-Access-Manager_1658794.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[With all the healthcare companies focusing on Switzerland companies in this industry are facing high competition. In this competitive world of healthcare sales it is important to have an excellent market access strategy. I am currently searching for one of my clients, a big, international health care company, a Market Access specialist with an international focus. I am searching for individuals with experience in market access in Switzerland and who are fluent in English and German, to be fluent in French would be an advantage. The company is offering you a position in a global, broad based health care company in an international team located in the German speaking part of Switzerland. Working for this company means that you will be working for a company which is recognised as a good place to work and which received numerous local, national and international distinctions. As the Market Access specialist you will be responsible for acting as a leadership member regarding market access subjects and you will contribute to the area strategy as well as to the tactic plans. Additionally the market access manager will be responsible for identifying and developing innovative payer solutions to establish and strengthen the portfolio of the company.  This position is a very senior position within the market access department, responsible for overseeing the overall market access operation. Additionally this position would play a critical role in shaping the market access department into a proactive and integrated function. I am a recruitment consultant working in Switzerland. I am specialised in HEOR, Market Access and Biometrics. If you want to get further information regarding this positions, or on many more like this, please do not hesitate to contact me on +41 435080972 or k.schirmer(at)realstaffing.com. I am looking forward to receiving your current CV as a word document.  Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, good place to work, international, pricingand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[CTA dringend gesucht für die Schweiz]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob5114835E8D6E904D482579F60022286E</referencenumber>
<City><![CDATA[Switzerland All]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/CTA-dringend-gesucht-f-and-amp-SHARP252r-die-Schweiz_1640268.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Unser Kunde ist ein fand#252;hrendes Unternehmen im Bereich Medical Devices. Das Unternehmen besitzt ein interkulturelles Netzwerk von Mitarbeitern in and#252;ber 80 Standorten weltweit. Am Schweizer Standort mand#246;chte das global agierende Unternehmen sein Clinical Operation Team erweitern und sucht daher einen engagierten Clinical Trial Assistant. Das Arbeitsumfeld ist sehr motivierend und liegt inmitten der schand#246;nen Schweizer Bergwelt, die Ski fahren, wandern und vieles mehr ermand#246;glicht.Die Clinical Trial Assistant Position ist eine sehr spannende und abwechslungsreiche Stelle im Clinical Operation Bereich, dies bedeutet, Sie werden das klinische Team mit verschiedensten unterschiedlichen administrativen Aufgabenbereichen unterstand#252;tzen, wie das Generieren von Daten, Vorbereitung von Dokumente und Protokollen, das Bearbeiten von Patientendaten und die Dokumentenpflege klinischer Akten. Zusand#228;tzlich bieten sich Aufstiegsmand#246;glichkeiten zum Lead CTA oder CRA durch interne Weiterbildungsmand#246;glichkeiten fand#252;r motivierte Mitarbeiter an.  Ein CTA-Kandidat sollte daher folgende Eigenschaften mitbringen wie einen universitand#228;ren Abschluss im Bereich klinischer Forschung oder in einem and#228;hnlichen Bereich, gute kommunikative Fand#228;higkeiten besitzen, sowie flieand#223;end deutsch und englisch sprechen, jede weitere Fremdsprache ist ein Plus. Des Weiteren sollten Sie ein motivierter und positiv denkender Mensch sein, der selbstand#228;ndig wie auch in einem internationalen Team arbeiten kann.Falls Sie sich angesprochen fand#252;hlen, dann senden Sie so schnell wie mand#246;glich Ihre aussagekrand#228;ftigen Bewerbungsunterlagen in Word Format  an Nadja Beckert n.beckert(at)realstaffing.com oder falls noch weitere Fragen haben die offen sind dann rufen Sie mich doch unter +41 (0)4350809728 an. Schweiz, Luzern, Zand#252;rich, klinische Studien, clinical Trial, Clinical Trial Assistant, klinische Projektassistenz, klinische Forschung, CRO, CPA, CRA, CTA, Pharmabereich, Switzerland, klinische Forschung, klinische Untersuchungen, Clinical Trial Assistant, klinische Mitarbeiter, SCRA, Senior CRA, Principal CRA, Kanton Zand#252;rich, Clinical Operation, Nadja Beckert, Studienbegleitung, Clinical Data Associate, Clinical Research Associates, Clinical Trial Manager, Clinical Studies, Study Managers, Klinisches Monitoring, Monitoring, CRO, CRA, Senior CRA, Senior CRO, Director Clinical Research, Head of Medical Studies, Head of Clinical Research, Clinical Project Managerand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Engagierter Market Access Manager mit nationalem Fokus]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob778A426095AAD8BD482579F60022288C</referencenumber>
<City><![CDATA[Berne]]></City>
<Country><![CDATA[SWITZERLAND]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Engagierter-Market-Access-Manager-mit-nationalem-Fokus_1640277.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Aufgrund der aktuellen Marktsituation sehen sich aktuell viele Unternehmen der Herausforderung gegenand#252;ber ein sehr starkes und wettbewerbsfand#228;higes Team im Bereich Market Access und Pricing and#38; Reimbursement zu haben. Aktuell unterstand#252;tze ich die Schweizer Niederlassung eines der grand#246;ssten Pharmaunternehmen weltweit bei der Identifikation von Talenten in Bereich Market Access, Governmental Affairs und Public Relation. Fand#252;r dieses Unternehmen suche ich einenMarket Access Manager mit einem Schweizer FokusDie Hauptaufgaben innerhalb dieser Funktion belaufen sich vor allem auf + Aufbau und Pflege eines starken Netzwerkes mit key stakeholder speziell mit dem BAG und verschiedenen Krankenversicherungen+ Entwicklung und Implementierung von Market Access Strategien fand#252;r neue Indikationen+ Zusammenarbeit mit verschiedenen internen Abteilungen sowie externen Organisationen um eine wettbewerbsfand#228;hige Market Access Strategie zu gewand#228;hrleisten + Entwicklung und Implementierung einer Pricing Strategie + Market Access Trainings fand#252;r verschiedene interne Abteilungen Fand#252;r diese Position suche ich eine engagierte Persand#246;nlichkeit, die bereits Erfahrung im Bereich Market Access in der Schweiz gesammelt hat. Sollten Sie bereits Erfahrung und ein Netzwerk in der Schweiz haben wand#228;re dies von Vorteil. Da sich die Position auf Onkologie fokussiert, suche ich vor allem jemanden, der bereits Erfahrung in diesem Bereich hat. Neben Sprachkenntnissen in Deutsch, Englisch und Franzand#246;sisch sollten Sie weiterhin noch einen Universitand#228;ren Abschluss, gerne im Bereich (Health) Economic, Law, etc. mitbringen. Wenn ich Ihr Interesse fand#252;r diese Position oder weitere Positionen im Bereich Biometrik und HEOR geweckt habe, freue ich mich and#252;ber eine Kontaktaufnahme um mit Ihnen verschiedene Mand#246;glichkeiten hier in der Schweiz zu besprechen. Sie kand#246;nnen mich unter +41 435080972 oder k.schirmer(at)realstaffing.com erreichen.Keyword: BAG, Switzerland, Schweiz, Suisse, Market Access, Pricing, German, English, Deutsch, Englisch, Franzand#246;sisch, French, international, health care, Market Access, Pricing, Reimbursement, pharma, Multinational Enterprise, MNE, Oncology, Onkologieand#60;Br/and#62;and#60;Br/and#62;(Real Staffing Group acts as an Employment Agency and an Employment Business)]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Mitarbeiter für meine Kunden in der Pharmaindustrie gesucht!]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobD76260D0D5D1F57C482579F6002228A7</referencenumber>
<City><![CDATA[Hessen]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Mitarbeiter-f-and-amp-SHARP252r-meine-Kunden-in-der-Pharmaindustrie-gesucht_1640354.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Meine Kunden sind Pharmaunternehmen, die verschiedene Indikationen und Bereiche abdecken, einige hiervon sind z.B. auch bekannte Generika Unternehmen, forschende Pharmaunternehmen sind natand#252;rlich ebenfalls in meinem Kundenstamm vertreten.Aufgrund der guten Marktsituation und des Wachstums der Unternehmen sind derzeit einige Stellen vakant die ich gerne besetzten mand#246;chte. and#220;berwiegend sind derzeit  Key Account Manager Positionen zu besetzten, diese in den unterschiedlichsten Bereichen sowie Indikationen. Sowohl die Definition des Key Account Manager als Innendiestmitarbeiter, also in eine kaufmand#228;nnische Richtung gehend, ist derzeit bei meinen Vakanzen vertreten als auch die eher typischen Key Account Manager Position im Auand#223;endienst, die z.B. die Aufgaben der Betreuung von Spezialkunden beinhaltet. Zudem suche ich verstand#228;rkt Brand Manager sowie Product Manager mit RX und/oder OTC Erfahrung ( 2 and#150; 3 Jahre Berufserfahrung sind Grundvoraussetzung) mit flieand#223;enden, verhandlungssicheren Englischkenntnissen in Wort und Schrift. Sie suchen derzeit eine neue Herausforderung in der Pharmaindustrie? Haben Ihr Studium der Medizin, Naturwissenschaft, BWL oder vergleichbaren erfolgreich abgeschlossen? Bringen einige Jahre Berufserfahrung aus der Pharmaindustrie mit?Dann schicken Sie bitte Ihre Bewerbungsunterlagen an: Lisa SchumacherReal Pharma Frankfurt   l.schumacher(at)realstaffing.comTel: 069 26489 8400Bei Fragen stehe ich Ihnen gerne zur Verfand#252;gung.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Supply Chain Manager Medizintechnik (wm) nahe Mannheim gesucht]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob380A970CCEE7B886482579F6002228B5</referencenumber>
<City></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State><![CDATA[Pfalz]]></State>
<url>http://www.engineer-job.eu/job/Supply-Chain-Manager-Medizintechnik-w-m-nahe-Mannheim-gesucht_1640357.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[and#60;band#62;Zum Aufbau- und weiteren Ausbau des Geschand#228;ftsbereiches Medizintechnik, Biotech und Pharmazie meines Kunden, ein stark international geprand#228;gtes Unternehmen nahe Mannheim, wird nand#228;chstmand#246;glich ein kompetenter Supply Chain Manager gesucht. and#60;/band#62;and#60;band#62;Ihre Aufgabenand#60;/band#62;Sie sind fand#252;r das komplette Supply Chain Management, dessen Gestaltung und stetige Weiterentwicklung verantwortlich. Der Einkauf von C-Artikeln, Rohstoffen etc. sowie  das Erstellen von Fertigungsauftrand#228;gen gehand#246;rt ebenfalls zu Ihren Aufgaben. Das Lagerbestandsmanagement sowie die Preisverhandlungen runden Ihr Portfolio ab. Sie sind die Schnittstelle zur Muttergesellschaft.and#60;band#62;Ihr Profiland#60;/band#62;Sie bringen ein abgeschlossenes Studium im Bereich Wirtschaftsingenieurwesen mit Schwerpunkt Maschinenbau oder Betriebswirtschaft mit Schwerpunkt Supply Chain Management mit. Erste Berufserfahrung and#252;ber einschland#228;gige Praktika oder ein abgeschlossenes Traineeprogramm sind von Vorteil. Technisches Verstand#228;ndnis bei der Weiterentwicklung des Bereiches Supply Chain Management sowie Interesse an Fand#252;hrungsverantwortung fand#252;r Mitarbeiter ist wand#252;nschenswert.Wenn Sie sich dieser verantwortungsvollen Aufgabe stellen mand#246;chten, senden Sie uns bitte Ihre aussagekrand#228;ftigen Bewerbungsunterlagen an folgende Kontaktdaten zu.  a.wydra(at) realstaffing.com / Agnes Wydra, Tel. 069 264 89 8400]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Quality Assurance and Compliance Manager]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob9840D22520B6474F482579F60022298B</referencenumber>
<City></City>
<Country><![CDATA[UK]]></Country>
<postalcode></postalcode>
<State><![CDATA[South East]]></State>
<url>http://www.engineer-job.eu/job/Quality-Assurance-and-Compliance-Manager_1640161.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[A leading Pharmaceutical Services organisation is currently recruiting for a UK Quality and Compliance Manager on behalf of a blue chip pharmaceutical company. Responsible for a UK Team you will be responsible for a the UK GXP Audit plan of all services including, distribution, supply chain, document solutions, GMP Cleaning, Lab Services and facilities management. Key responsibilities include:Manage the UK Quality and Compliance team, to ensure that resources are appropriately applied and utilised, in the delivery of quality and compliance support to the operational teams.Manage the UK Quality and#38; Compliance team to aid the development and continuous improvement of the Global Quality Management System. Work with cross functional teams to investigate, root-causes analyse and implement corrective actions where GxP deficiencies are discovered.Present quality related topics to local business management. Perform investigations and special projects as required by senior management.Maintain communication with key business and client personnel.Provide guidance and assistance to Quality and Compliance staff.Conduct training in GxP and QMS topics, to the wider operations team.Assist the Business development teams in bidding / securing new business.If you are interested in this position you must have the following experience to relevant in your application:- Previous Management experience- Previous Pharmaceutical Audit Experience- Previous Experience in Quality Assurance The position is based in Hertfordshire and looking to pay up to and#163;45k plus benefits, if you wish to apply please send an updated CV to John Morkus or call 0207 758 7311 for further details.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Drug Safety Physician (mw) gesucht]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob2CE532B648855071482579F6002229A0</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Drug-Safety-Physician-m-w-gesucht_1640173.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Drug Safety Physician (m/w) gesuchtFand#252;r ein weltweit fand#252;hrendes, forschendes Pharmaunternehmen suche ich ab sofort einen and#60;band#62; Safety Physician (m/w) and#60;/band#62;!Aufgaben:and#149;In der Klinischen Entwicklung auf Augenhand#246;he als Persand#246;nlichkeit auftretenand#149;Schreiben von Risk-Management Pland#228;nenand#149;Unterstand#252;tzung bei Produkteinfand#252;hrungenand#149;Vertretung der gesamten Pharmakovigilanz Perspektiven im pre- und post-marketingFand#252;r diese Stelle sollten Sie folgende and#60;band#62; Eigenschaftenand#60;/band#62; nachweisen kand#246;nnen:and#149;Abschluss eines Medizinischen Studiums, eine Facharztausbildung ist von Vorteiland#149;Praktische Erfahrung in der Klinischen Forschungand#149;Fundierte Erfahung in der Pharmakovigilanzand#149;flieand#223;endes und sicheres Deutsch und Englisch in Wort und SchriftGerne erhalten Sie diskret und fachlich kompetent weitere Details. Ihr Ansprechpartner ist Hanna HolowatyTel. +49 (0) 69264 898400and#60;/band#62;Senden Sie mir Ihren CV im and#60;band#62; WORD Formatand#60;/band#62;, max. 1MB, and#252;ber den Online Bewerbungslink oder an and#60;band#62; h.holowaty(at)realstaffing.com and#60;/band#62;und rufen Sie mich an. Weiterhin besetze ich deutschlandweit weitere Positionen, als Festanstellungen, im Bereich der Pharmakovigilanz und im Medical Affairs. Gerne stelle ich Ihnen unverbindlich neue Mand#246;glichkeiten vor und biete neue Perspektiven.Besuchen Sie mein XING Profil fand#252;r weitere Informationen.https://www.xing.com/profile/Hanna_Holowaty]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[URGENT  Los Angeles  Clinical Contracts Associate]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJobA304E972748F8468482579F6002229B1</referencenumber>
<City></City>
<Country><![CDATA[USA]]></Country>
<postalcode></postalcode>
<State><![CDATA[San Diego]]></State>
<url>http://www.engineerjob.us/job/URGENT-Los-Angeles-Clinical-Contracts-Associate_1658799.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[My client has a need for  a Clinical Contracts Associate that will negotiate with research sites, ensure contracts are written associated with CRMD, and apply clinical principles to solutions of problems with the following experience;-minimum of six plus years of analytical experience or equivalent. -Familiarity with grant and contract requirements, policies, and procedures including, but not limited to:               -Clinical and AdvaMed Code of Ethics on Interactions with                  HealthCare Professionals.               -Knowledge of federal, state and industry rules and regulations governing technical aspects of grants and contracts.                -Requires a demonstrated knowledge of the practices/procedures of the function, company polices, and programs.               -Requires demonstrated written and verbal communication, interpersonal, presentation, technical, analytical, statistical, organizational, and follow-up skills, the ability to meet deadlines as well as the ability to converse effectively with all levels of employees.              -Must be able to demonstrate and use discretion in exercising work assignments and handle sensitive/confidential information in an effective manner.           - Must have the demonstrated ability to understand and comply with applicable government regulations and Company operating procedures, processes, policies, and tasks.            -Must have demonstrated personal computer skills including a working familiarity with relevant word processing, database, and spreadsheet applications (i.e., Microsoft Word, Excel and Access). Desired Requirements: -Paralegal certification preferred.- Previous related experience administering and/or coordinating grant and/ or contract requests in medical device, biologics, or pharmaceutical company.  -Registered nurse, legal, clinical research associate experience desired. -An advanced degree (i.e., masters and/or doctorate level) as well as professional certifications (i.e., Certified Professional Contracts Manager (CPCM), Certified Clinical Research Professional (CCRP), or related certifications) also a plus.This role needs to be filled by Friday. Please send your resume immediately if interested.]]></description>
<salary></salary>
<education></education> 
<jobtype></jobtype>
<category>Pharmaceuticals &amp; Biotechnologys</category>
<experience></experience>
</job>
<job>
<title><![CDATA[Freelance CPM Bavaria 6 months 5days 50% Onsite, 50 % Homebased]]></title>
<date>Sun, 06 May 2012 00:00:00 GMT</date>
<Closedate>Thu, 05 Jul 2012 00:00:00 GMT</Closedate>
<referencenumber>ExpatJob86E6B46CE6D09462482579F6002229C4</referencenumber>
<City><![CDATA[Bayern]]></City>
<Country><![CDATA[GERMANY]]></Country>
<postalcode></postalcode>
<State></State>
<url>http://www.engineer-job.eu/job/Freelance-CPM-Bavaria-6-months-5days-50-Onsite-50-Home-based_1670003.html</url>
<company><![CDATA[Real Staffing]]></company>
<description><![CDATA[Freelance Clinical Project Manager/ in Bavaria/ 6 months/ 5days/ 50% Onsite, 50 % Home-basedMy client is a large Pharmaceutical Company based in Bavaria who is looking for a Freelance Clinical Project Manager with experience in Non- Interventional Studies. Key Responsibilities:and#149;Responsible for conducting interventional (phaseIIIb, IV trials) and non Interventional studies (Registries, Post Authorization studies) in the CV therapeutic areaand#149;Leadership of a cross- functional international study teamand#149;Matrix Management of PAN European trials ensuring that all trial deliverables are met according to timelines, budget and resource requirementsand#149;Supervision of preparation and submission of all relevant study documents to authorities and regulatory bodies and their follow upand#149;Responsible for writing trial protocols, eCRF, project plans, trial reports, publicationsand#149;Management of study related Steering Committeeand#149;Daily Management of Vendorsand#149;Development of clinical outsourcing specifications with CROs and other 3rd partiesand#149;Contribution to the implementation of best practices and standards for trial management, including sharing lessons learnedand#149;Training of internal CRA regarding trial requirements and#149;Close collaboration with Medical Affairs with assuring that Study design meets the global medical strategy and#149;Representation of Clinical Operations in brand teamsand#149;Organisation and charing investigator meetings and team meetings Expertise and Complexity:and#149;University degree in medicine or natural sciences with a minimum of 5 years experience in the pharmaceutical industry, doctored preferred and#149;Minimum of 5 years experience in clinical research and international project management and#149;Thorough knowledge of Clinical Research Principles , ICH- GCP , EU regulations governing clinical trials, standard regulatory and clinical practices an
