Commissioning Engineer
Job in
4800, Breda, North Brabant, Netherlands
Listed on 2026-05-14
Listing for:
Talentmark
Full Time
position Listed on 2026-05-14
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below
The CQV Engineer will support technical projects under minimal supervision and will report to Sr Manager Validation & Compliance within the site Engineering organization. The CQV Engineer will demonstrate hands on commissioning/qualification skills, including but not limited to the following: develop, implement, and report test strategies for technical solutions in accordance with internal customer requirements and standard CQV procedures. The CQV Engineer will drive the development of system commissioning qualification and validation documentation.
Key Responsibilities
Documentation:
Develop and update several Validation documents (System Level Criticality Assessments, Validation, Commissioning, Qualification plans, Risk assessments, Test Protocols, Requirement traceability matrixes, Commissioning, Qualification and Validation summary reports)
Testing: Lead commissioning, qualification and validation activities.
Technical support: Deliver guidance to the project group, ensuring the implementation follows the validation plan to meet internal customer requirements and company SOPs.
Qualifications & Experience
Experienced with secondary packaging systems, including print and inspection systems (e.g., Systech, Cognex).
At least 3 years’ experience in executing commissioning, qualification and validation within manufacturing organizations in the pharmaceutical industry.
Experienced in Computerized Systems Validation.
Hands‑on commissioning and qualification experience within secondary packaging operations.
Ability to work independently and remotely with minimum direct supervision (a plus).
Ability to anticipate, evaluate and resolve multiple, simultaneous project issues, delays and problems by utilizing technical and business expertise (a plus).
Interested in this opportunity? Please respond via this page!
Seniority level
Associate
Employment type
Full-time
Job function
Biotechnology Research and Pharmaceutical Manufacturing
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