Job Description
documentation for licensing, compliance and extension of licenses to the Drug Administration.
- Following up obtaining approvals for drug testing, such as manufacture permission etc.
- Monitoring sent files(from the factory)reviewing with Ministry of Health experts and providing necessary responses to resolve any possible bugs.
- Performing follow-up on bug fixes and questions related to the health department from the relevant units in the factory.
- Examining the specifications of new products, manufacturing methods and used materials and the role of each according to the relevant formulation and reference standards and used pharmacopoeia.
- Reviewing and controlling the materials analysis sheets used in new products, methods of materials analysis and their compliance with reference standards and relevant pharmacopoeias.
- Reviewing and controlling new product brochures in terms of drug name and form, storage conditions, warnings, etc., and ensure the compliance with established standards.
- Supervising and updating the records of current products and taking the necessary actions and required coordination to extend their licenses.
- Attending to joint meetings in unit or others to solve possible problems and improve production conditions and product quality.
- Assisting in conducting research and studies on the implementation of R&D projects from a technical view, economic and profitability point of view, and preparing analytical reports in this regard