Job Description
● Compiling and submission activities for licenses under the supervision of the RA manager, as well as reviewing the list of documents required for submission and providing on-time product information as needed.
● Assisting RA in monitoring the regulatory environment and ensuring compliance.
● Providing sufficient information on local regulatory requirements to other departments.
● Drafting routine correspondence to IFDA concerning import, release, and distribution permissions.
● Participating in the planning, performing, and following up on internal and external inspections.
● Creating and managing effective communication and close collaboration with MOH and related organizations.
