CQV Engineer

Proclinical

Oberwallis

On-site

CHF 110,000 - 150,000

Full time

33 hours ago
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Job summary

Proclinical is seeking a CQV Engineer to support commissioning, qualification, and validation activities for systems, equipment, and processes throughout their lifecycle. The role requires ensuring regulatory compliance and managing technical changes, with the right to work in Switzerland or EU passport.

Proclinical is acting as an Employment Agency in relation to this vacancy. The candidate will plan, coordinate, and perform qualifications; evaluate changes; prepare TCRs; handle deviations and

Qualifications

  • Plan, coordinate, and perform qualifications of plant units and equipment.
  • Evaluate changes, conduct periodic reviews, and support decommissioning.
  • Prepare, process, and coordinate Technical Change Requests (TCRs).
  • Ensure timely handling of deviations, investigations, and CAPAs, assessing impact on qualified state.
  • Create, review, and release CQV documentation per GxP requirements.
  • Act as CQV SME for project teams, QA, and operations, guiding on maintain qualified state.
  • Represent department during audits, customer visits, and regulatory inspections.

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.

Skills

Attention to detail
Independent work
Excellent communication

Education

Technical degree or equivalent experience

Tools

Kneat
MS Word
MS Excel
MS PowerPoint

Job description

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).

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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