QA Validation Specialist PQR

vor 2 Wochen

Sitten, Schweiz Jobs via eFinancialCareers Vollzeit
QA Validation Specialist PQRSwisslinx Sion, Schweiz Jetzt bewerben Gepostet vor 17 Stunden Befristet Competitive

On behalf of our client, a leading international biotechnology company based in Visp, Swisslinx is looking for a QA Validation Specialist PQR. In this role, you will lead quality assurance efforts by driving process validation excellence, managing Product Quality Reviews (PQRs), ensuring compliance with GMP standards, and acting as a key liaison during customer audits.

Contract type - Contract
Start Date - January
Location - Visp
Workload - 100%
Duration - 12 months

Your Mission

  1. Ensure the trainings required to the Process Validation Specialist with focus on Product Quality Review are completed.
  2. Active participation and contribution to the validation team to ensure the experience is shared and the practices are further developed.
  3. Support the project teams to ensure compliance with company SOPs and related documents.
  4. Preparation and approval of the monthly PQR Newsletter.
  5. Maintenance of the PQR status overview list CHVI-204288.
  6. Participation in the preparation of process specific PQRs review and approval of PQRs.
  7. Evaluation and approval of change requests, deviation and SOPs concerning PQRs.
  8. Contact person for PQR/CPV during customer audits.

Your Background
  1. Degree in the Life Sciences, Pharmacy, Engineering, or a related field.
  2. 5+ years experience in a similar role.
  3. Proven experience in process validation, Product Quality Reviews (PQRs), and working within GMP-regulated environments in the pharmaceutical or biopharmaceutical industry.
  4. Familiarity with quality systems, including change control, deviation management, and SOP development, as well as experience with customer audits and compliance evaluations.
  5. Ability to contribute actively to cross-functional teams, ensuring training, knowledge-sharing, and alignment with organizational best practices.
  6. Strong organizational skills to maintain PQR status overviews, prepare newsletters, and handle complex documentation and reporting tasks efficiently.
  7. Confidence in liaising with internal teams and external customers during audits, ensuring clear and effective representation of quality processes.

What's on offer
  1. A 12 month contract.
  2. A great opportunity to develop your career at a leading international biotechnology company.
  3. A competitive salary.

If this sounds like the right fit for you, don't hesitate to apply For more information, please reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com. #J-18808-Ljbffr

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