QA Specialist / Batch Record Review (m/f/d)
- Review executed electronic and/or manufacturing protocol for compliance to GMP
- Support implementation/ revision of manufacturing protocols for GMP manufacturing
- 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
- 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
- A very renowned company
- A highly motivated team and an open way of communication
À propos de l'entreprise
