Job Description
-Food supplement & Drug registration applications in a timely manner and in accordance with yearly
-Well-established connection with MOH and often visiting the MOH officers for registration of new products or extension over the approval of current products.
-Handles product safety, reviewing individual adverse event reports, aggregate adverse event statistics, and able to make a good connection with KOLs and medical advisors.
-Ensure packs with first time launches or variations to folding box, label or leaflets are in accordance with product specifications and within compliance standards
-Maintenance of a professional relationship with Ministry of Health and monitor competitive activities
-Establish and maintenance of Health Authority Stakeholder mapping
-Follow ups on Contract Manufacturing operations