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Senior Qualification Engineer

Job in 3930, Visp, Canton du Valais, Switzerland
Listing for: R&D Partners
Full Time position
Listed on 2026-02-14
Job specializations:
  • Engineering
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: Visp

Ready to engineer precision in the world of biotech? Join our client's cutting-edge team and play a vital role in developing the instrumentation that powers tomorrow's breakthroughs.

R&D Partners is seeking a Senior Qualification Engineer to join our client in Visp on a permanent basis. In this role, you will play a key part in supporting the development and qualification of equipment and processes for a new manufacturing site. This is an exciting opportunity to contribute to the creation of safe and effective injectable treatments for patients.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Plan and manage qualification projects for a new manufacturing site.
  • Define strategies for commissioning, qualification, and validation (CQV).
  • Work with external specialists, supervise their work, and ensure quality standards are met.
  • Conduct qualifications independently, including design qualification (DQ), installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).
  • Support factory acceptance tests (FATs) and site acceptance tests (SATs).
  • Maintain equipment in a qualified state and plan requalifications as needed.
  • Perform periodic reviews and update qualification concepts based on new standards and technical advancements.
  • Represent the department during audits and inspections.

Key Skills and Requirements:

  • Educational background in engineering, pharmaceutical technology, medical technology, chemistry, process engineering, or a related field.
  • Strong knowledge and experience in plant qualification within a GMP-regulated environment.
  • Good understanding of GMP standards, technical processes, and safety protocols.
  • Ability to work independently and manage multiple projects effectively.
  • Strong communication and organizational skills.

For more information, please contact William Hay.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners 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 -

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Position Requirements
10+ Years work experience
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