CQV Engineer (Commissioning, Qualification & Validation)
About the role
βοΈ CQV Engineer β Commissioning, Qualification & Validation
π Switzerland (On-site) | π Full-time | π° Salary based on profile
DQ β Commissioning β IQ/OQ/PQ
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, youβll work on-site with major clients, supporting high-impact industrial projects from installation to validation.
π§© Your Role
- 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
π§ Your Profile
- Bachelorβs or Masterβs in Engineering, Pharmaceutical Sciences, or related field
- 3+ years CQV experience in GMP pharma/biotech
- Strong knowledge of GMP and regulatory requirements
- Bonus: autoclaves qualification / cleanroom validation
- Fluent in German and/or English
π Why agap2
- Long-term, stable role in Switzerland
- Challenging projects with industry leaders
- Certified training and career development
- Supportive local management & strong team culture
Requirements mentioned in the advert
These excerpts come from the advert text held by Panta. They may differ from the employerβs latest posting. Missing or unclear evidence does not mean a requirement is optional. Confirm the full requirements with the employer.
English: unclear
β’ Fluent in German and/or English
German: unclear
β’ Fluent in German and/or English
Workload: unclear from the available text
Automatic text checks can miss context.