Job Duties
* Searching for the innovative 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 inquiry requests and applications originating from government agencies for registration & re-registration of different pharmaceutical products.
* Co-work with nominated departments' 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.
Qualifications, experience, and skills required
* BSc of Pharmacy
* From 0 to 2 years of experience in Regulatory Affairs.
* Very good English is a must.
* Excellent computer skills.
* Having good communication and presentation skills.
* Hard worker, self-motivated, and encourages teamwork
Job Category
Registration
###### **About Zahrawi Group** Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, & Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, & Analytical Industries. #####…
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