- 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
- 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.
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