Quality Assurance/Batch Record Review (m/f/d)

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