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Executive – Regulatory Affairs

Sun Pharma
Sun Pharma
2-5 years
Not Disclosed
Vadodara, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Executive – Regulatory Affairs (US Group) Job in Vadodara | Sun Pharma Careers

Company: Sun Pharmaceutical Industries Ltd.
Job Title: Executive – Regulatory Affairs (US Group)
Department: R&D Regulatory Affairs
Location: Vadodara (Baroda), Gujarat, India
Job Type: Full-Time
Industry: Pharmaceutical / Regulatory Affairs / Drug Development


About Sun Pharma

Sun Pharmaceutical Industries Ltd. is one of the world’s leading specialty generic pharmaceutical companies, known for delivering high-quality and innovative healthcare solutions across global markets. With a strong focus on research, regulatory excellence, and pharmaceutical innovation, Sun Pharma continues to expand its global regulatory and product development capabilities.

The company offers a collaborative and growth-oriented environment where professionals can enhance their expertise in regulatory affairs, clinical development, and pharmaceutical compliance.


Job Overview

Sun Pharma is seeking an experienced Executive – Regulatory Affairs (US Group) to join its R&D Regulatory Affairs team in Vadodara. The selected candidate will be responsible for supporting global regulatory submissions, preparing CTD/eCTD dossiers, coordinating with cross-functional teams, and ensuring compliance with USFDA, ICH, and regional regulatory requirements.

This role is ideal for regulatory affairs professionals with expertise in pharmaceutical dossier compilation, global submission management, and regulatory lifecycle support for US and international markets.


Experience Required

Experience Level

  • Mid-Level Regulatory Affairs Professional
  • Freshers are not eligible

Required Experience

  • Minimum 2–5 years of relevant experience in:
    • Regulatory Affairs
    • Pharmaceutical Regulatory Submissions
    • Dossier Preparation
    • Global Regulatory Compliance

Preferred Industry Experience

  • Pharmaceutical Industry
  • Generic Drug Development
  • Global Regulatory Operations
  • US Regulatory Affairs

Educational Qualification

Required Qualification

  • Master of Pharmacy (M.Pharm)