Job Description

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...

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