<ul><li>Submit regulatory applications for new product registrations, renewals, and variations</li><li>Review and finalize technical documents including specifications, analytical methods, and manufacturing process</li><li>Respond to regulatory queries from global health authorities and ensure timely follow-up</li><li>Maintain regulatory databases, track submissions, and update internal records</li><li>Ensure compliance with applicable regulatory guidelines such as ICH, WHO, USFDA, EMA, and local authorities</li><li>Participate in regulatory audits and inspections, preparing required documentation and justifications</li></ul><p>&nbsp;</p>

Sr. Officer-QA (DRA)