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Quality Assurance Specialist
Job in
3930, Visp, Canton du Valais, Switzerland
Listed on 2026-01-11
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
Job Description & How to Apply Below
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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