Work from Office
Full Time
Roles and Responsibilities Prepare dossiers for regulatory submissions, including CTDs and RA dossiers. Conduct document reviews to ensure compliance with drug regulatory affairs requirements. Provide expertise on dossier preparation, drug regulatory affairs, and related matters. Collaborate with cross-functional teams to achieve project goals. Ensure timely submission of regulatory documents to relevant authorities. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) from a recognized institution. 3-5 years of experience in pharmaceutical industry with a focus on drug regulatory affairs. Strong understanding of CTD, Document Review, Dossier Preparation, and RA processes.
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