Regulatory Affairs Us Noida

Regulatory Affairs Us Noida

02 Oct
|
Naari Pharma
|
Noida

02 Oct

Naari Pharma

Noida

Role & responsibilities
Prepare and submit CTD/ACTD dossiers for 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 Us Noida
🏢 Naari Pharma
📍 Noida

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