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- 50+ years experience - Deep subject-matter expertise - Global Life Sciences network
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Commissioning Qualification Validation Engineer (GMP) - Engineering, Quality Assurance - Netherlands, Breda - July 16, 2026 - Fulltime - V-195775 - Competitive
Vacancy: CQV Engineer - GMP
For an international pharmaceutical manufacturing organisation, we are looking for two experienced Commissioning, Qualification and Validation Engineers .
You will support technical projects within a GMP-regulated environment and be responsible for developing and executing commissioning, qualification and validation documentation and activities.
Key requirements - At least three years of CQV experience within pharmaceutical manufacturing - Hands-on experience with secondary packaging systems - Experience with print and inspection systems, such as Systech or Cognex - Experience with Computerized Systems Validation - Knowledge of HVAC qualification, CQV and CSV - Strong technical writing and communication skills in English - Ability to work independently and manage multiple project priorities
Location: Breda area, the Netherlands
Contract: 12 months, with possible extension
Start date: As soon as possible
Working arrangement: Onsite, five days per week
Important: Candidates must live within reasonable commuting distance of Breda and be available to work onsite five days per week.
Relocation candidates cannot be considered.
Applicants must already hold a valid Dutch work permit or have an unrestricted right to work in the Netherlands.
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