- Support all Regulatory Affairs activities in order to achieve and maintain registrations in compliance with all national and regional Regulatory and legal obligations
- Batch release and control and release of manufacturing and test documentation
- Coordinate, preparing, executing and post processing inspection by national and international authorities as well as supplier audits
Requirements
- Pharmacist (Pharm D.) with valid Pharma license.
- Good knowledge and experience in pharmaceutical manufacturing (Medicine and Food Supplement) and quality control of aseptic dosage form.
- Fluency in English language.
