CQV Engineer
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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 regulatory requirements
- Fluent in German and/or English
Why agap2
- Challenging projects with industry leaders
- Certified training and career development
- Supportive local management & strong team culture
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