On-Site GMP CQV Engineer: Validation & Commissioning Lead

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

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.