Verification and Validation Engineer for the Medical Device Sector

Presentation

On behalf of one of our clients we are now looking for a highly motivated Verification and Validation Engineer, with previous experience in developing verification/validation plans, test procedures and reports, for a temporary assignment in Uppsala. The assignment which is full-time will start in March 23, 2015, and continue until September 25, 2015. The review of candidates will commence immediately, so please submit your application as soon as possible.

Arbetsuppgifter

The main focus in the role as Verification Engineer is to lead, plan and execute verification of customized BioProcess products. You will be working in a team of approximately 10 validation and Verification Engineers and report to the Section Manager Verification.

Key responsibilities include:
- functional test planning of products within Customized BioProcess Solutions (CBS)
- functional testing of products within CBS
- reject/approve test results within CBS
- check and approve/reject other verification engineers' test records
- improve and develop verification of CBS products
- lead and guide verification activities
- report defects product nonconformance
- participate in customers Factory Acceptance Testing (FAT)
- participate in technical discussion with customers
- participate in development of procedures for functional testing
- maintain and develop competence required
- support service with maintenance and repair of customized equipment

Utbildning/erfarenhet

For this role we require that you have the following education and experience:
- Bachelor’s degree in Biomedical Engineering, Electrical Engineering or closely related discipline or similar knowledge from working experience
- demonstrated experience in developing verification/validation plan, test procedure and reports
- demonstrated experience in leading verification
- GMP knowledge
- English and Swedish as working languages, both written and spoken

It is also desired that you have a previous knowledge from GE Healthcare Bioprocess Products.

Apart from the above stated requirements, we also see that you have the following characteristics:
- structured/analytical
- self-starter, energizing, and able to multi-task
- demonstrated problem solving ability and result orientation
- service minded

Förmåner

We take good care of our consultants and we offer social activities, as well as help in planning your future career. Your consultant manager is well experienced from your field, and knows how to get the most out of your assignment.

As a Poolia employee, you are included in the requirements concerning agreements on terms of employment by Unionen. Moreover, you get a grant for working out at your choice of place. You are also covered by a health insurance.

Företagsbeskrivning

Poolia Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

Sluttext

Please apply by registering your CV here on our website. Click on the "Ansök" button to the right of this advertisement. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail adress is registered.

Poolia is a registered staffing agency, meaning that we comply with the requirements set by Bemanningsföretagen - the Swedish Association of Staffing Agencies.

Language

en-GB