31 Oct
|
U S Pharma India
|
India
31 Oct
U S Pharma India
India
Role & responsibilities :
Prepare, compile, review, and submit regulatory dossiers (CTD/eCTD/ACTD) for product registration, renewal, and variation.
Respond to regulatory authority queries within stipulated timelines.
Review product labels, artworks, leaflets, and packaging to ensure regulatory compliance.
Coordinate with internal departments such as QA, QC, Production, R&D;, and Marketing.
📌 Regulatory Affairs Officer Mumbai (India)
🏢 U S Pharma India
📍 India