- Batch release and control and release of manufacturing and test documentation
- Monitoring and continual further development of Q.A system, including monitoring critical Quality Parameters
- Coordinate, preparing, executing and post processing inspection by national and international authorities as well as supplier audits
- To ensure manufacturing was carried out in compliance with GMP
- Manufacturing and testing procedure are validated
Requirements
- Doctorate of Pharmacy
- Very good knowledge and experience in pharmaceutical manufacturing and quality control of aseptic dosage form
- Good knowledge of current GMP regulation
- Pronounced sense of responsibility
- Decision making abilities and assertiveness
- Team work and organizational skills.