- Create and manage effective communication and close collaboration with FDO/MOH
- Necessary actions and follow-ups to receive related permissions from FDO/MOH
- Supervise the implementation of MOH regulations and SOPs for production activities and submission of related reports and technical documents
- Validate API and supplier according to GMP standards
- Monitor the result of quality control done by reference laboratories
- Issue release permission of product distribution
- Check and confirm the batch manufacturing records
- Focus on continuous improvement of production methods in order to ensure quality and safety of products
- Conduct frequent internal audit of production site and warehouses
Requirements
• Education: Pharmacist (Pharm D)
• Experience: Minimum of 2 years as a responsible pharmacist in biotech pharmaceutical companies
• Capabilities: Good knowledge of GMP and MOH regulation, Production Process and quality control - Strong communication skills – Planning skills – Managerial skills - Fluent in English