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QA Specialist

Job in 3930, Visp, Canton du Valais, Switzerland
Listing for: Proclinical Group
Full Time position
Listed on 2026-01-11
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Visp

Looking for a role where quality isn't just a checkbox but a mission? Join our client as a QA Specialist and elevate your career in a dynamic CMO environment.

Proclinical is seeking a QA Specialist to act as a key quality assurance contact, ensuring compliance and supporting manufacturing operations. This position focuses on quality oversight, regulatory compliance, and continuous improvement initiatives.

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
  • Represent QA in project teams and meetings, serving as the primary contact for quality‑related topics.
  • Address drug product QA‑related questions, topics, and customer complaints tied to manufacturing operations.
  • Support and approve risk assessments, including regulatory‑specific risks or gap analyses.
  • Review and release product‑specific documentation such as process descriptions, workflows, manufacturing protocols, transfer documents, test plans, and parameter lists.
  • Represent drug product QA during regulatory inspections.
  • Contribute to continuous improvement programs to enhance the Quality Management System.
  • Collaborate with cross‑functional teams, including manufacturing, QC, support functions, and engineering, to ensure effective execution of drug product processes.
  • Assess, review, and approve quality records and release files, including deviations, change controls, CAPAs, investigations, effectiveness checks, complaints, and APR/PQRs, in line with local SOPs.
Key Skills and Requirements
  • Degree in Chemistry, Biology, Biotechnology, or a related field.
  • Experience working in a GMP‑regulated pharmaceutical environment.
  • Background in quality assurance, particularly in drug product QA.
  • Proficiency in English;
    German language skills are advantageous.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at

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 -

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