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 ResponsibilitiesLead commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilitiesDevelop and execute protocols (IQ/OQ/PQ) in compliance with EU GMP standardsEnsure alignment with Annex 1 requirements for sterile manufacturing environmentsCollaborate with cross‑functional teams including QA, Engineering, and Regulatory AffairsProvide technical oversight and troubleshooting during project executionSupport documentation, reporting, and audit readinessCandidate ProfileProven CQV experience within pharma/biotech manufacturing (mid to senior level)Strong knowledge of EU GMP, Annex 1, and regulatory frameworksTrack record of delivering CQV projects in sterile or complex manufacturing environmentsExcellent communication and stakeholder management skillsFull rights to work in France/EUAvailability to relocate and work across different sites in FranceWhy Apply?Opportunity to contribute to high‑impact projects in a global pharma/biotech environment12‑month contract with strong likelihood of extensionPipeline of upcoming senior CQV roles offering career progressionExposure to diverse sites and cutting‑edge manufacturing technologiesNext StepsInterested candidates are invited to apply now with an updated CV. Shortlisted applicants will be contacted to discuss project details and relocation support.