<ul><li>Prepare and compile regulatory submissions for product registrations and approvals.</li><li>Ensure compliance with local and international regulatory guidelines (CDSCO, USFDA, EMA, WHO, etc.).</li><li>Coordinate with R&amp;D, QA, QC, and Production teams for regulatory documentation.</li><li>Respond to regulatory queries and deficiency letters in a timely manner.</li><li>Maintain and update regulatory files, databases, and records systematically.</li><li>Monitor changes in regulations and support implementation of compliance measures.</li><li>Assist in regulatory inspections, audits, and internal compliance reviews.</li><li>Support preparation of dossiers like CTDs, DMFs, and technical reports.</li></ul>

Sr. Executive-Regulatory Affairs