- Effective communication and close collaboration with MOH.
- Preparing and submitting Documents such as CTD, PMF to IFDA.
- Preparing pricing documents.
- Daily follow-up and hard work for receiving responses and results.
Requirements
Requirements:
- At least 2 years of experience in the regulatory field and pharmaceutical company
- Familiar with regulatory affairs and MOH procedures
- Familiar with GMP requirements.
- Familiar with pricing procedure in IFDA.
- Team work skills.
- English proficiency.