Job Description
Title: Quality Specialist
Location: Visp, Valais, Switzerland (On-site)
We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.
This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive actions.
Responsibilities:
Conduct thorough and well-documented investigations of deviations in the manufacturing process of monoclonal antibody-based products.
Perform root cause analyses using structured methodologies (e.g., 5-Why, Ishikawa, FMEA).
Develop, implement, and follow up on corrective and preventive actions (CAPAs).
Collaborate closely with teams from Production, QA, QC, and Development to comprehe...
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Submit ApplicationJob Details
- Location Visp, Valais
- Job Type Full-time
- Category ATS
- Posted Date February 28, 2026
- Application Deadline April 09, 2026