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CQV Engineer (Commissioning, Qualification & Validation)

  • Bern, Bern, Schweiz

About the role

βš™οΈ CQV Engineer – Commissioning, Qualification & Validation

πŸ“ Switzerland (On-site) | πŸ•“ Full-time | πŸ’° 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, you’ll work on-site with major clients, supporting high-impact industrial projects from installation to validation.

🧩 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

🧠 Your Profile

  • 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
  • Bonus: autoclaves qualification / cleanroom validation
  • Fluent in German and/or English

πŸš€ Why agap2

  • Long-term, stable role in Switzerland
  • Challenging projects with industry leaders
  • Certified training and career development
  • Supportive local management & strong team culture

These excerpts come from the advert text held by Panta. They may differ from the employer’s 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.