Role & responsibilities

We are looking for an experienced Regulatory Affairs skilled who will be responsible for end-to-end regulatory submissions and dossier management for Nepal Markets. Candidate will be responsible for managing end-to-end Regulatory Affairs activities for the Nepal market.

- Candidate will be responsible for preparation, compilation and submission of regulatory dossiers to Nepal authorities.
- Candidate will be responsible for registration and renewal of pharmaceutical products including tablets, syrups and other formulations.
- Candidate will be responsible for regulatory submissions, follow-ups, queries and approvals with Nepal regulatory authorities.
- Candidate will be responsible for ensuring compliance with applicable Nepal regulatory requirements and timelines.




- Candidate will be responsible for coordinating with internal teams for dossier preparation and regulatory submissions.

Candidate Profile

- Candidate should have 710 years of relevant experience in Regulatory Affairs.
- Candidate should have extensive hands-on experience in the Nepal pharmaceutical market.
- Candidate should have hands-on experience in dossier preparation and product registration in Nepal.
- Candidate should have experience handling registration of products such as tablets, syrups and other pharmaceutical formulations.
- Candidate should have strong knowledge of Nepal regulatory requirements and submission processes.
- Candidate should be willing to work exclusively on the Nepal market.

📌 Regulatory Affairs Executive (Mumbai)
🏢 HRD House
📍 Mumbai