Sr Exe

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr Exe Date: Jun 3, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Job Summary Regulatory submission of new products, renewals, variations, response to queries and Life cycle management for MENA markets through preparation of quality dossiers enabling timely approvals.Area of Responsibility New submissions/Renewals: Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions. Review documents (Development report, scale up report, specification, stability protocol), artworks etc. before initiation of Exhibitbatches for adequacy. Approval: Review & prepare response to deficiency enabling approval of products filed to regulatory agency. Lifecycle management for drug formulations: Prepare and review variations as per the country specific requirements to support approval of changes such as API vendor changes/changes in ROS/test parameters; DF site changes; harmonization of products etc. Regulatory compliance: Prepare, Review and circulate approval package with product history sheet to stake holders upon receipt of approval and updatethe same based on queries and variations. Ensure reposition of comprehensive product information into central repository Review regulatory filing impact of variations, change controls, etc.Geographic Scope/ Market MENA-GCC, UAE, Oman, Saudi Arabia, Egypt, Iran, Iraq, Bahrain etc.) Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less