CQV Engineer (Commissioning, Qualification & Validation)

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

Benefits offered by this job

Challenging projects

Training and career development

Solid local leadership

Job summary

agap2 is seeking a CQV Engineer for on-site work in Switzerland. You will support validation activities from installation through commissioning and qualification, ensuring GMP compliance and timely delivery.

This role requires 3+ years in CQV within pharma/biotech, fluency in German or English, and a strong track record of DQ/IQ/OQ/PQ execution, risk assessment, and collaboration with vendors. Join a team with challenging projects and strong local leadership.

Qualifications

• Bachelor's or Master's in Engineering, Pharmaceutical Sciences, or related field.
• 3+ years CQV experience in GMP pharma/biotech.
• Fluent in German and/or English.

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.

Education

Engineering or Pharmaceutical Sciences degree

Tools

CQV protocols

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