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 regulatory requirements
• Fluent in German and/or English

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Why agap2

• Challenging projects with industry leaders
• Certified training and career development
• Supportive local management & strong team culture