Job Description

● Register the products at the commerce department. ● Prepare and deliver the required documents for releasing the goods from the TTAC. ● Help with preparing documents for regulatory issues. ● Support in collecting and coordinating information and preparing regulatory documentation for submission to regulatory affairs. ● Perform basic and advanced GMP affairs. ● Review and control brochures. ● Follow up the registration process at the MOH.

Requirements

● Master's degree in Chemistry, Biochemistry, Microbiology, or Pharmacy. ● Ability to do teamwork. ● Good social relationships. ● Accurate, patient, and interested in learning. ● Fluent in Microsoft Office. ● Fluent in English. ● Ability to communicate effectively and continuously with the Food and Drug Administration, trade unions, and related bodies. ● Familiar with GMP principles. ● Familiarity with the instructions for speeding up the drug registration process and the systems of the Food and Drug Administration.

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