Title:  Exe/ Sr Exe

Date:  May 15, 2024
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 Botswana/Namibia/South Africa markets through preparation of quality dossiers enabling timely approvals. Area of Responsibility
1. New submissions/Renewals:
a. Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.
b. Review documents (Development report, scale up report, specification, stability protocol), artworks etc. before initiation of Exhibit batches for adequacy.
2. Approval:
Review & prepare response to deficiency enabling approval of products filed to regulatory agency.
3. Lifecycle management for drug formulations:
a. 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.
4. Regulatory compliance:
a. Prepare, Review and circulate approval package with product history sheet to stake holders upon receipt of approval and update the same based on queries and variations.
b. Ensure reposition of comprehensive product information into central repository
C. Review regulatory filing impact of variations, change controls, etc. Geographic Scope/ Market
EM-5 (South Africa), Botswana, Namibia