Sun Pharma Hiring Global Regulatory Affairs Executive/Sr. Executive

Global Regulatory Affairs Pharma Jobs – Sun Pharma Hiring M.Pharm Graduates in Gurgaon, Mumbai, Baroda

Sun Pharmaceutical is inviting applications for Executive/Sr. Executive roles in Global Regulatory Affairs (Specialty Pharma). M.Pharm candidates with experience in CMC, regulatory filings, and IND/IMPD preparation can apply. Location: Gurgaon, Mumbai, Baroda.

M.Pharm Jobs at Sun Pharma – Regulatory Affairs Openings in Gurgaon, Mumbai, Baroda

Regulatory Affairs Jobs for M.Pharm Professionals – Join Sun Pharmaceutical

Sun Pharmaceutical Industries Ltd, a global leader in generic and specialty pharmaceuticals, is actively hiring for the Global Regulatory Affairs – Specialty Pharma department. The company is offering Executive and Sr. Executive roles across Gurgaon (preferred), Baroda, and Mumbai locations.

If you’re an experienced M.Pharm graduate with hands-on expertise in regulatory filings, CMC documentation, and IND/IMPD preparation, this opportunity positions you at the forefront of regulatory strategy in one of India’s top pharma organizations.

Job Designation and Location Details

• Position: Executive / Sr. Executive
• Grade: G11A / G11B
• Department: Global Regulatory Affairs (Specialty Pharma)
• Location: Gurgaon (preferred), Baroda, Mumbai
• Education: M.Pharm

Key Responsibilities

1. Support and manage regulatory activities associated with Chemistry, Manufacturing, and Controls (CMC) for global New Drug Applications.
2. Handle regulatory filings, query responses, and post-approval changes across various global markets including US, EU, Japan, China, and other regulated/non-regulated markets.
3. Perform gap assessments and support data generation by collaborating with cross-functional teams.
4. Coordinate with global consultants and local regulatory teams to understand region-specific requirements.
5. Prepare Agency consultation packages, briefing books, and participate in regulatory consultations.
6. Draft and manage IND (Investigational New Drug) and IMPD (Investigational Medicinal Product Dossier) documentation.
7. Align regulatory strategies with global manufacturing sites and regularly update senior management.

Preferred Candidate Profile

• M.Pharm with 2–8 years of experience in regulatory affairs
• Strong knowledge of global regulatory requirements (especially for regulated markets)
• Experience with IND/IMPD documentation, agency interactions, and CMC regulatory strategy
• Proactive communication and cross-functional collaboration skills

Why Choose Sun Pharma?

• Exposure to global regulatory frameworks
• Work with a high-performing regulatory team
• Growth-oriented and innovation-driven environment
• Opportunity to contribute to specialty pharma developments

How to Apply

Apply now via the official Sun Pharma Careers portal: Apply Here

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