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Job Title: Drug Regulatory Affairs Executive Industry: Pharmaceutical / Healthcare Experience: 13 Years Qualification: B.Pharm / M.Pharm / M.Sc. (Pharmaceutical Sciences) Location: Rai Sonipat Key Responsibilities Prepare and review regulatory dossiers and submission documents.Handle CTD/eCTD submissions, renewals, variations and registrations.Coordinate with CDSCO, State FDA and other regulatory authorities.Respond to regulatory queries and maintain authority communication.Coordinate with QA, R&D, Production and Pharmacovigilance teams.Track regulatory updates and ensure compliance with applicable guidelines.Maintain regulatory records, databases and documentation.Key Skills Regulatory Submissions (CTD/eCTD)Dossier Preparation & ReviewKnowledge of Indian & Global Regulatory GuidelinesHealth Authority CommunicationDocumentation & MS OfficeAttention to Detail and Time ManagementPay: 241,761.71 - 1,184,485.78 per year Work Location: In person .