• Plan and manage regulatory submissions in SG.
• Plan and support regulatory submissions in our regional markets.
• Compile registration dossiers and ensure timely submission to the authorities.
• Perform duties of Responsible Person as per HSA guidelines.
• Maintenance of registered importer’s, wholesaler’s, product licenses and support activities to ensure compliance.
• Manage activities related to Quality Assurance, Pharmacovigilance and adverse events reporting.
• Achieve the targets set and account for ADVAGEN's regulatory submissions and activities.
• Provide updates and reports of the above duties and responsibilities.
• Support other projects that may be assigned by the Director including tenders, marketing and new products.
