CQV Engineer (Commissioning, Qualification & Validation)

Switzerland (On-site) | Full-time | Salary based on profile

You turn complex systems into GMP-compliant operations.

At agap2 , a European engineering services company founded in 2005, we support leading projects across Pharma, Biotech, Medical Devices, and Chemicals. As a CQV Engineer, you’ll work on-site with major clients, supporting high-impact industrial projects from installation to validation.

• Execute and approve DQ, IQ, OQ, and PQ activities
• Ensure CQV milestones and timelines are met
• Supervise vendors and validate commissioning quality
• Generate and review validation protocols, reports, and technical documentation
• Track deviations, non-conformances, and CAPAs
• Assess project risks and implement corrective actions
• Bachelor’s or Master’s in Engineering, Pharmaceutical Sciences, or related field
• 3+ years CQV experience in GMP pharma/biotech
• Strong knowledge of GMP and...