Job Description
Commissioning, qualification & validation engineer
Adryan is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the life sciences industry. We are specialised in the areas of project management, engineering, CQV and compliance.
As a hands‑on CQV engineer, you are part of a project team and are responsible for the commissioning, qualification and validation activities of GMP facilities, process equipment and critical building and utility systems within our client’s life sciences production facility. This includes the design, implementation and documentation of these qualifications and their lifecycle management, in compliance with all applicable regulatory and internal quality standards (FDA and/or EU regulations).
Key responsibilities
- Within a smoothly running project team, you’ll be accountable for all aspects of CQV activities as required by schedule an...
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