06 Aug
|
Vee Excel
|
Delhi
-Prepare, review, and submit CTD/eCTD/ACTD dossiers for international product registrations.
-Ensure compliance with regulatory requirements in EU, US, Asia, CIS, LATAM, and Africa.
-Coordinate with regulatory agencies/client for product approvals.
Required Candidate profile
Bachelor’s/Master’s degree in Pharmacy, Pharmaceutical Sciences
5–10 years of experience in international regulatory affairs.
Robust knowledge of ICH, WHO-GMP, and country-spec regulatory guidelines.
📌 Drug Regulatory Affairs Executive (Delhi)
🏢 Vee Excel
📍 Delhi