QA Batch Record
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Quality Assurance Specialist – Batch Record
Key Responsibilities:
- Review electronic and/or manufacturing protocols to ensure compliance with GMP standards.
- Support the implementation and revision of manufacturing protocols for GMP-compliant production.
- Ensure adherence to internal and external GMP standards, as well as regulatory requirements, in all projects.
- Participate in cross-functional investigations to assess product quality impact and define corrective actions.
- Act as the Quality Unit representative in cross-functional teams, making independent quality decisions based on regulatory knowledge and offering quality support to project teams.
- Review and approve validation documents.
Key Requirements:
- Degree in Biology, Chemistry, Biotechnology, Life Sciences, or a related field, or relevant experience in the pharmaceutical industry.
- Experience in a GMP-regulated pharmaceutical environment is preferred.
- Fluency in English is required; proficiency in German is an advantage.
**Please only apply if you are eligible to work in Switzerland and the EU**
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