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Job Description
- Searching for innovator products of the newly required generic product, to acquire complete scientific feedback concerning the product's active raw materials, their strengths, delivered dosage form, and the product potency.
- Complete all inquiries requests and applications originating from government agencies for registration & re-registration of different pharmaceutical products.
- Co-work with the R&D department, which supplies the registration with a steady stream of data and technical details required for registration files.
- Filling all data for the company and government agencies according to specific requirements of each file: Technical file, NODCAR file, Stability Study file, In vitro Comparative Dissolution Studies.
Job Requirements
- BSc of Pharmacy/ Vet./ Science
- 1-2 years of experience in Regulatory Affairs.
- Very good English is a must.
- Excellent in computer skills.
- Having good communication and presentation skills.
- Hard worker, self-motivated, and encourages teamwork.