Regulatory Affairs Executive
Department
Regulatory
Location
Mumbai, Maharashtra
Experience
2–5 years
Employment type
Full-time
Positions
1
Posted
9 August 2026
About the role
Handle product licensing, label approvals and correspondence with the state drugs authority, and keep our regulatory filings current as the portfolio grows.
You will work closely with R&D and Quality to make sure what is on the label matches what is in the pack, every time.
You will work closely with R&D and Quality to make sure what is on the label matches what is in the pack, every time.
What we are looking for
A degree in pharmacy or a related field.
Working knowledge of Indian drug regulatory requirements (D&C Act, Schedule M).
Precise, unhurried attention to documentation detail.
Working knowledge of Indian drug regulatory requirements (D&C Act, Schedule M).
Precise, unhurried attention to documentation detail.