Regulatory Affairs Agent

Job Description

1. Analyze broad-scope implications of changing regulations and guidance.
2. Registration of required classified products.
3. Serve as Central Reference point for all regulatory affairs both AMICO and its supplier in Kuwait.
4. Assist as needed in providing necessary documentation or information to support import and export of regulated products, including regulatory certificates for Medical Devices.
5. Monitor the impact of changing regulations on submission strategies and update internal stakeholders.
6. Assist in regulatory due diligence for potential and new acquisitions. Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities.
7. Represent AMICO to authorities in the Ministry of Health whenever required.
8. Licensing from MOH for advertisement for suppliers.
9. Represent AMICO wherever required.

Candidate Requirements

1. Min 2-3 yrs of experience in Regulatory but not limited to.