- To monitor compliance with the principles of GMP in devolving the pharma plant
- To monitor compliance with the principles of cGMP in production
- To communicate proactively with IFDA regard establishment of production site and registration of products
Requirements
- A good understanding of the relevant IFDA (Terms and Rules)
- Fluent in all principles of GxP
- Effective time management and Communication skills
- Fluency of English is required.
- Gender: No preferences
- Age: 25-40