CQV Engineer (Commissioning, Qualification & Validation)

agap2 Switzerland; Basel; On-site; CHF 110,000 - 150,000; Full time

Job summary

agap2 Switzerland is seeking a CQV Engineer to support on-site GMP pharma/biotech projects in Basel. You will execute and approve DQ/IQ/OQ/PQ activities, ensure milestones, and supervise vendors to validate commissioning quality.

The role requires a Bachelor’s or Master’s in Engineering or Pharmaceutical Sciences and 3+ years CQV experience in GMP environments, with fluent German and/or English. On-site role with career development opportunities.

Qualifications

• 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.

Responsibilities

• 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

Skills

CQV experience

GMP knowledge

Regulatory knowledge

German/English language

Education

Bachelor’s or Master’s in Engineering/Pharma Sciences

Tools

Validation protocols

Technical documentation

Job description

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