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Quality Assurance Specialist

Job in 3930, Visp, Canton du Valais, Switzerland
Listing for: K-Recruiting Life Sciences
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

QA Specialist

We unite the people who make our world healthier by placing top experts with life sciences companies worldwide. Precise. Fast. Accurate.

Tasks:

  • Represent Quality Assurance in project teams and participate actively in cross‑functional meetings to ensure quality considerations are integrated into all project phases.
  • Serve as the primary QA contact for designated topics, including the coordination and oversight of DRs and CRs.
  • Act as the point of contact for Drug Product QA matters, addressing customer inquiries, operational questions, and complaints related to manufacturing activities.
  • Support, evaluate, and approve risk assessments, including regulatory‑driven risk or gap analyses.
  • Review and release product‑specific documentation such as process descriptions, workflows, recipes, manufacturing protocols, transfer documents, test plans, and parameter lists.
  • Represent Drug Product QA during regulatory inspections and contribute to inspection readiness activities.
  • Drive and support continuous improvement initiatives aimed at strengthening the Quality Management System at Visp DPS.
  • Collaborate closely with Manufacturing, QC, Support Functions, and Engineering teams to ensure seamless execution of Drug Product processes and technology transfers.
  • Assess, review, and approve quality records and release documentation (e.g., deviations, change controls, CAPAs, investigations, effectiveness checks, complaints, APR/PQRs) in accordance with current SOPs and GMP requirements.

Qualification:

  • University degree in Chemistry, Biology, Biotechnology, or a related scientific discipline.
  • Extensive experience working in a GMP‑regulated pharmaceutical environment.
  • Proven background in Quality Assurance within Drug Product operations.
  • Strong understanding of pharmaceutical manufacturing processes, quality systems, and regulatory expectations.
  • Excellent communication and stakeholder‑management skills, with the ability to collaborate effectively across functions.
  • Fluency in English;
    German language skills are considered an advantage.
  • Strong organizational skills and the ability to manage priorities in a dynamic environment.

Requirements:

  • Start: 02.02.2026
  • Duration: 6 months

Seniority level:
Associate

Employment type:

Full‑time

Job function:
Quality Assurance

Industries:
Staffing and Recruiting

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