QA Batch Record Reviewer
vor 2 Wochen
QA Batch Record Reviewer
Location:
Visp, Switzerland
Start Date:
01 January 2026 – 30 September 2026
Workload:
100%
Language:
English (C1), German skills preferred
About the Role
We 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 Do
- Review 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 For
- Academic 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
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