- +1
- Switzerland
À propos
Job Responsibilities
- 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.
Compétences idéales
- Chemistry
Compétences linguistiques
- English