Regulatory Affairs AssociateRegulatory CTD / ACTD dossiers

Noida, UP Full time

View details

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 recent roles open.

Apply

Submit your application

Share your details and attach your resume our team reviews every application and responds to shortlisted candidates within two weeks. Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Regulatory Affairs Associate Noida (India)
🏢 Biodeal Pharmaceuticals
📍 India