QA Specialist / Batch Record Review (m/f/d)

Ihre Aufgaben:
• 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

Ihre Qualifikationen:
• 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

Ihre Vorteile:
• A very renowned company
• A highly motivated team and an open way of communication

Projektdauer: 6 MM


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