Regulatory Affairs Specialist

M.Pharm Regulatory Affairs Openings - 2 to 12 Years Exp - Baroda & Gurgaon Explore M.Pharm job opportunities in Regulatory Affairs (US & ROW markets) at Sun Pharma - 2-12 years experience - Baroda & Gurgaon. Join Sun Pharma’s Regulatory Affairs Department - Opportunities at Baroda & Gurgaon Sun Pharma, one of India’s leading pharmaceutical giants, is currently hiring experienced professionals in the Regulatory Affairs department for its Baroda and Gurgaon locations. This is a great opportunity for candidates with an M.Pharm degree and hands-on experience in global regulatory submission processes. The roles are open across two major regulatory regions - ROW (Rest of the World) and US/Europe. Current Job Openings A) Regulatory Affairs - ROW (Russia, CIS, APAC, Africa, LATAM) Key Requirements: Education: M.Pharm Experience: 2 to 12 years in regulatory submissions Familiarity with ROW market regulations including Russia, CIS, APAC, Africa, Brazil, and LATAM Experience in dossier preparation and submission Strong understanding of international regulatory landscapes B) Regulatory Affairs - US/Europe Key Responsibilities: Education: M.Pharm Experience: 2 to 6 years Compilation and review of dossiers for regulated markets: US, EU, AU, Canada, Israel (orals/non-orals) Review of query responses prepared by regulatory associates Assessment of documentation from stakeholders related to dossier compilation, life cycle management, and regulatory queries Why Join Sun Pharma? Be part of India’s largest pharma company with a global footprint Work in a high-compliance, innovation-driven regulatory team Opportunities for continuous learning, growth, and global project exposure #J-18808-Ljbffr