CQV Engineer
This is a contract position with a leading pharmaceutical/biotech organization, requiring candidates to hold full rights to work in France/EU. Successful applicants will support commissioning, qualification, and validation (CQV) activities across multiple French sites. The role offers strong potential for extension and progression into more senior opportunities.
Key Responsibilities
- Lead commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilities
- Develop and execute protocols (IQ/OQ/PQ) in compliance with EU GMP standards
- Ensure alignment with Annex 1 requirements for sterile manufacturing environments
- Collaborate with cross‑functional teams including QA, Engineering, and Regulatory Affairs
- Provide technical oversight and troubleshooting during project execution
- Support documentation, reporting, and audit readiness
Candidate Profile
- Proven CQV experience within pharma/biotech manufacturing (mid to senior level)
- Strong knowledge of EU GMP, Annex 1, and regulatory frameworks
- Track record of delivering CQV projects in sterile or complex manufacturing environments
- Excellent communication and stakeholder management skills
- Full rights to work in France/EU
- Availability to relocate and work across different sites in France
Why Apply?
- Opportunity to contribute to high‑impact projects in a global pharma/biotech environment
- 12‑month contract with strong likelihood of extension
- Pipeline of upcoming senior CQV roles offering career progression
- Exposure to diverse sites and cutting‑edge manufacturing technologies
Next Steps
Interested candidates are invited to apply now with an updated CV. Shortlisted applicants will be contacted to discuss project details and relocation support.
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