Key Responsibilities:

Product Registration:

Handle product registration for dietary supplements and medical devices in accordance with legal requirements.
Coordinate and closely collaborate with the FDA, partners, production, and quality control teams to prepare accurate registration documents within specified timelines.

Documentation:

Prepare documents for drug registration renewals and related licenses.
Submit, amend, and update product registrations as assigned.
Plan and track the status of submitted registration documents, and organize them for easy access and retrieval.

Regulatory Compliance:

Ensure licenses and registrations for drugs and medical devices comply with current regulations and are efficiently implemented.
Submit product samples for quality testing and verify product labels against FDA requirements before production.

Coordination:

Liaise with government officials and agencies.
Report registration status and communicate relevant legal updates from the FDA to all concerned parties.

Qualifications:

Bachelor's degree in Pharmacy (with a professional license in pharmacy)
Experience in the registration of modern pharmaceuticals.
Experience in handling drug registration responsibilities.
Intermediate or higher proficiency in English.
Strong proficiency in computer programs such as MS Office and other standard software used with FDA systems and related agencies.
Knowledge and understanding of drug registration guidelines and regulations.
Ability to work and communicate effectively with colleagues across all departments and maintain a positive and open attitude.