About the job
Job Purpose - Responsible for product registration with MOH, as well as the fulfillment of all regulatory requirements to import, market, and utilize AMICO products.
Key Responsibilities.
Awareness about the implications of changing regulations and guidance.
Responsible to apply for MOH initial and final Permit.
Responsible to do MOH permit payments.
Follow up on the applied permit request status.
Familiar with U.A.E MOH import and export regulations for medical device items.
Familiar with the U.A.E MOH Batch release process.
Candidate Preference.
Minimum Graduate or Bachelor's Degree (Pharmacy, Science etc) but not limited to.
Certificate in Pharmacovigilance preferred but not limited to.
1 to 5 years of work experience in Regulatory Affairs in the U.A.E.
Seniority Level: Other
Job Functions: Legal & Compliance
Industries : Information Technology
