- Handle regulatory activities for Nepal, Bhutan and other APAC markets.
- Prepare and compile ACTD dossiers and regulatory documents.
- Coordinate with cross-functional teams for required documentation and submissions.
- Support product registrations, renewals, variations and regulatory queries.
- Maintain regulatory documentation and track submission timelines.
Key Skills: ACTD dossier knowledge, positive documentation and communication skills, cross-functional coordination, attention to detail, and basic understanding of APAC regulatory requirements. Qualification: M.Pharm
Experience: Fresher, 6 months-1 year in Regulatory Affairs