Offer summary
Qualifications:
Degree in science; 7+ years in biopharmaceuticals, MSc in Industrial Pharmaceutical Science preferred, 3+ years supervisory experience in manufacturing, Experience in aseptic filling and sterilisation, Track record in audit and regulatory management.
Key responsabilities:
- Ensure compliance with product quality standards
- Oversee adherence to EU GMP and FDA regulations
- Perform checks, tests, and quality documentation
- Update teams on technical advancements
- Collaborate with global QA and operations teams