Regulatory Affairs AssociateRegulatory CTD / ACTD dossiers

Noida, UP Full-time

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Prepare and manage CTD / ACTD dossiers and product registrations for Indian and international markets helping take our products into regulated destinations.

What youll do

• Compile and maintain CTD / ACTD dossiers

• Manage product registrations and renewals

• Liaise with regulatory authorities and partners

• Track evolving regulatory requirements across markets

What were looking for

• B.Pharm / M.Pharm

• 13 years in regulatory affairs

• Exposure to export-market filings (a plus)

• Excellent written communication

Positions are managed via our CMS and refreshed as new roles open.

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