CQV Engineer - Onsite Location: Leiden, Netherlands
Contract: 12 months (with possible extension)
Industry: Pharmaceutical / Biotech
Work Type: Onsite Role Overview Experienced CQV Engineer to support commissioning, qualification, and validation activities at a GMP-regulated pharmaceutical site in Leiden.
12-month onsite contract with the potential for extension, offering hands-on involvement in active manufacturing and project environments.
Suited to professionals with strong technical experience who enjoy working close to the plant floor and contributing directly to GMP compliance and project delivery.
Key Responsibilities
Execute commissioning, qualification, and validation (CQV) activities for GMP equipment, utilities, and facilities
Prepare and execute IQ, OQ, and PQ documentation
Support commissioning and engineering handover activities
Contribute to URS, risk assessments, and validation documentation
Identify and document deviations and support change control activities
Ensure all CQV documentation is accurate, compliant, and inspection-ready
Collaborate with Engineering, QA, Automation, and Operations teams
Requirements
Degree in Engineering, Life Sciences, or a related technical discipline
Proven experience as a CQV Engineer in a GMP-regulated pharmaceutical or biotech environment
Hands-on experience with equipment and/or utilities qualification
Good understanding of GMP principles and the validation lifecycle
Ability to work fully onsite in Leiden
Fluent in English
Nice to Have
Experience with clean utilities (WFI, clean steam, HVAC)
Exposure to aseptic or sterile manufacturing environments
Experience supporting CAPEX projects
What’s on Offer
12-month contract with possible extension
Onsite role at a leading life sciences site
Immediate involvement in GMP qualification projects
Interested?
Please apply or send your CV directly to: s.jetten@panda-int.com