Quality Assurance/Batch Record Review LZAJP00004474
Duration: Until 31 March 2025/possible extension
Key responsibilities:
- Ensure that internal/ external GMP standards and regulatory requirements are adhered to in projects.
- Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
- Represent the Quality Unit in cross-functional teams. Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
- Review and approve validation documents.
Key requirements:
- Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry
- Previous experience in GMP regulated pharmaceutical industry is an advantage
- English fluency and German good command is an advantage
- Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
- Excellent verbal, written and interpersonal communications skills
About the company
