Our client is a multinational biologics manufacturer based in the Haut-Rhin department of Alsace. They are searching for a CQV Engineer specialising in upstream cell culture equipment to join them on a long-term contract. The position can be recruited at engineer, senior or lead level. The CQV (Commissioning, Qualification, Validation) Engineer will be responsible for:
- The development, execution, review and approval of all CQV Documents relating to upstream USP cell culture systems.
- Commissioning, Qualification and Validation activities on upstream USP cell culture equipment.
- Act as Area Lead for upstream systems Seed Bioreactors Skids, Production Bioreactors Skids, media addition Skids, Single Use Bioreactors)
The successful candidate will be degree educated and have experience in commissioning and qualification of upstream USP cell culture equipment within a GMP biologics capital project. Fluency in English is required. French language skills are highly desirable.
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Abde Alaoui on +33 1 78 90 67 00 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.