● 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.