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Confirmed on the employer's own hiring board on Nov 7, 2026. First seen by Alion on Nov 4, 2026.

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Proclinical is a life sciences recruitment and consulting firm headquartered in London that provides executive search, permanent and contract staffing and workforce solutions exclusively to pharmaceutical, biotech, medical device and related companies. Founded in 2005, it runs offices across Europe, North America and Asia-Pacific, including Basel, and places candidates with clients in Switzerland, the UK, the US and Australia. Its current listings are client roles such as scientists, automation and instrumentation engineers, GCP quality managers, project coordinators, finance analysts and veterinary technicians.

Keep the heartbeat of innovation running! Join our client in this CQV Engineer and ensure cutting-edge manufacturing never miss a beat!

Proclinical is seeking a CQV Engineer to support commissioning, qualification, and validation activities for systems, equipment, and processes throughout their lifecycle. This role involves ensuring compliance with regulatory standards as well as managing technical changes.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

  • Plan, coordinate, and perform initial and periodic qualifications of plant units, systems, and technical equipment.
  • Evaluate technical changes, conduct periodic reviews, and support decommissioning activities.
  • Prepare, process, and coordinate Technical Change Requests (TCRs).
  • Ensure timely handling of deviations, investigations, and CAPAs, assessing their impact on the qualified state.
  • Create, review, and release technical and quality-relevant documentation in adherence to GxP requirements.
  • Act as a CQV Subject Matter Expert for project teams, engineering, QA, and operations, providing guidance on maintaining the qualified state of systems.
  • Represent the department during internal and external audits, customer visits, and regulatory inspections.
  • Present CQV documentation and support the resolution of audit findings.

Key Skills and Requirements:

  • Technical degree or equivalent professional experience in a relevant field.
  • Proficiency in Kneat, MS Word, Excel, and PowerPoint.
  • High attention to detail, precision, and ability to work independently with minimal supervision.
  • Strong verbal and written communication skills, with the ability to collaborate effectively in cross-functional teams.
  • Business fluency in German (required) and English (preferred).

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at [email protected].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.

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