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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