CQV Engineer

Vor 5 Stunden

Bern, Canton of Bern, Schweiz agap2 Switzerland Vollzeit
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