Global Regulatory Affairs Specialist – US & ROW

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.

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.

• 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

• 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

• 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