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 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 Exhibitbatches 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 updatethe 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 MENA-GCC, UAE, Oman, Saudi Arabia, Egypt, Iran, Iraq, Bahrain etc.) We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.