16 Aug
|
KNVM MEDICARE
|
Ghaziabad
16 Aug
KNVM MEDICARE
Ghaziabad
Role & responsibilities :- DOSSIER PREPARTION, ACTD,CTD,ROW.ASEAN, DOUMENTS REVIEW, MAINTAIN DOUMENTS.
ng Records (BMR), Specification & Test Procedures, and Stability Data.
Preferred candidate profile :- B. Pharm / M. Pharm or a postgraduate degree in Clinical Research/Regulatory Affairs.
2 to 5 years of core experience in international regulatory affairs.
Deep understanding of ICH guidelines, ASEAN guidelines, and country-specific ROW regulations. Hands-on experience with eCTD submission software and document management systems. Excellent technical writing, robust analytical skills, high attention to detail, and a sharp focus on deadlines.
📌 Drug Regulatory Affairs Executive (Ghaziabad)
🏢 KNVM MEDICARE
📍 Ghaziabad