1. Author and review regulatory dossiers, applications, variations, and regulatory responses.
2. Prepare and submit responses to WHO and other health authority queries.
3. Conduct regulatory impact assessments for change controls in e-QMS.
4. Review MFRs, specifications, and supporting documents for regulatory submissions.
5. Monitor and interpret regulatory guidelines, circulars, and health authority requirements.
6. Support implementation of new or revised regulatory requirements across relevant functions.
7. Coordinate with cross-functional teams for recent product development and lifecycle management.
8. Prepare and update dossiers for post-approval changes and variations.
9. Review regulatory responses prepared by team members for accuracy and compliance.
10. Prepare monthly regulatory updates and support other activities assigned by the HoD/Reporting Manager.
Preferred candidate profile Candidates having Vaccine experience will be preferred.