CQV Engineer - Manufacturing - Pharmaceuticals - 12-Month Contract Our client, a global biotechnology organisation, is recruiting for a CQV Engineer to join their capital project in Toulouse. This new build facility will house a therapeutic protein production plant, and we are looking for a CQV Engineer to help expand our client's biotech operations throughout Europe. As the CQV Engineer you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.
Responsibilities and Requirements:
- 5 to 10 years experience in qualifying UpStream and DownStream manufacturing equipment
- Experience in execution on equipment such as: Bioreactor, skid, Low Flow Chromatography skid, TCU Purification, Autoclave, Bag integrity tester, Centrifuge,
- Mastery of writing non-compliance management.
- Knowledge of Delta V is a plus
- Autonomous, flexible, collaborative Role: You will join the manufacturing equipment qualification execution team on our client's site located in Toulouse.
- Execute manufacturing equipment qualification protocols
- Manage qualification non-conformities (investigation, assessment, CAPA proposal)
If this role is of interest to you, please apply now!
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