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Quality & Regulatory

Regulatory Affairs Executive

Chandigarh (Head Office) Full Time 2–4 years in pharma regulatory documentation 1 opening

Role Overview

Prepare and maintain product permissions, manage state licensing documentation, coordinate with manufacturing partners for COAs, stability data and dossier updates.

What We're Looking For

B.Pharm / M.Pharm with knowledge of CDSCO and state licensing processes
Hands-on experience with Form 25/28 documentation
Strong documentation and follow-up discipline

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