QA Batch Record Reviewer

QA Batch Record Reviewer📍 Location: Visp, Switzerland📅 Start Date: 01 January 2026 – 30 September 2026💼 Workload: 100%🗣 Language: English (C1), German skills preferredAbout the RoleWe are looking for a QA Batch Record Reviewer to join a leading life sciences organization in Visp. In this role, you will ensure compliance and accuracy of production documentation, supporting batch release and maintaining the highest quality standards in a GMP-regulated environment.What You’ll DoReview executed batch records, including production documentation and raw data.Ensure completeness of documentation packages for batch release.Clarify comments with operations teams and evaluate with QA Managers.Support initiation of deviations and investigations related to batch record observations.What We’re Looking ForAcademic degree OR relevant experience in Biology, Chemistry, Biotechnology, or related field.Previous experience in GMP-regulated pharmaceutical or API industry is an advantage.Strong ability to identify non-compliance and gaps from quality standards.Structured, precise, and well-organized working attitude; open-minded, agile, and highly motivated.✅ Interested? Apply directly via LinkedIn or reach out for more details. This is your chance to contribute to high-impact projects in a dynamic environment!*While we appreciate every application, please note that due to the high volume of responses, we may only be able to contact shortlisted candidates.**Please note that we can only consider EU/Schengen applications