10 Sep
|
Naari Pharma
|
India
10 Sep
Naari Pharma
India
Role & responsibilities
Prepare and submit CTD/ACTD dossiers for ROW & US markets.
Handle product registrations, renewals, variations, and line extensions.
Review CMC documentation, stability data, and product dossiers.
Respond to regulatory queries and coordinate with cross-functional teams.
Preferred candidate profile
Experience in OSD dossier preparation
📌 Regulatory Affairs Row Or Us Noida (India)
🏢 Naari Pharma
📍 India