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Open nowPosted 2 days ago

CQV Engineer

Coopers Group AG

Where
Wallis, Switzerland
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Your applicationOpen nowCQV EngineerCoopers Group AG · Wallis, Switzerland

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 2 days ago

The posting

  • Life Sciences - Engineering Operations
  • Wallis
  • Contracting
  • Teilzeit, 100%
  • As soon as possible - 30.04.2027
  • CQV, GMP, CAPA

Location: Visp

Contract start date: As soon as possible

Contract end date: 30 Apr 2027

Responsibilities

  • Qualification & Re-qualification: Plan, coordinate, and perform initial and periodic qualifications of plants, units, systems, and technical equipment across their lifecycle. Evaluate technical changes, conduct periodic reviews, and support decommissioning activities.
  • Technical Changes & Deviation Management: Prepare, process, and coordinate Technical Change Requests (TCRs). Ensure timely handling of deviations, investigations, and CAPAs, assessing their impact on the qualified state.
  • Documentation & Compliance: Create, review, and release technical and quality-relevant documentation adhering strictly to GxP requirements. Ensure full traceability of all commissioning, qualification, and re-qualification activities.
  • Subject Matter Expertise (SME): Act as CQV Subject Matter Expert for project teams, Engineering, QA, and Operations. Provide guidance on technical measures and maintaining the qualified state of systems.
  • Audit & Inspection Support: Represent the department during internal/external audits, customer visits, and regulatory inspections. Present CQV documentation and support resolution of audit findings.

Requirements:

  • Technical degree (HF / FH / Applied Sciences / University) or equivalent professional experience in a technical field.
  • Fluent German and English
  • 3-5 years of professional experience in CQV, qualification, validation, or engineering within the pharmaceutical, biotech, or life sciences industry.
  • Experience working in a GMP-regulated manufacturing or laboratory environmen
  • Proficient with Kneat, MS Word, Excel, and PowerPoint.

Posting text belongs to the employer. Removal requests: contact us.

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