Bangalore SENIOR EXECUTIVE KA
Biocon Biologics
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Job description
The Team Member – GRA – Lifecycle Management supports post-approval regulatory activities to ensure continuous compliance of pharmaceutical products across global markets. This includes assisting with regulatory variations, renewals, labeling updates, and health authority commitments to maintain product registrations throughout their lifecycle. Academic Stream 0 Work experience (in months) 0 Job Responsibility and key Decisions Assist in preparing and submitting postapproval regulatory variations and renewals. Maintain accurate records of lifecycle submission statuses and health authority correspondence. Support crossfunctional teams by providing regulatory input on manufacturing, quality, and labeling changes. Review documents for regulatory compliance and completeness. Track and report on submission progress and timelines. Help manage responses to regulatory authority queries. Ensure adherence to internal SOPs and global regulatory standards. Key Decisions Identify and escalate potential issues in lifecycle submissions. Prioritize daily tasks based on submission deadlines. Report gaps or discrepancies in regulatory documentation Apply now Safe Harbour Cookie Policy Privacy Policy Terms of Use © 2026, Biocon. All Rights Reserved