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Senior Executive- India Regulatory Affairs

Sun Pharma
Sun Pharma
8-10 years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Executive – India Regulatory Affairs

Job Code: Manager II – India Regulatory & Business Continuity
Date Posted: January 3, 2026
Company: Sun Pharmaceutical Industries Ltd
Business Unit: R&D1 – Regulatory Affairs
Job Grade: G11A
Location: Baroda (Vadodara), Gujarat, India
Work Location: Tandalja – R&D
Employment Type: Full-time


About Sun Pharmaceutical Industries Ltd

Sun Pharmaceutical Industries Ltd is one of the world’s leading pharmaceutical companies, committed to delivering high-quality, affordable medicines globally. At Sun Pharma, we believe in empowering professionals to “Create Your Own Sunshine” by fostering continuous learning, ownership, and collaboration in a supportive and performance-driven environment.


Job Overview

Sun Pharma is seeking an experienced Senior Executive – India Regulatory Affairs to support regulatory strategy, dossier preparation, and submissions for pharmaceutical products in India. This role is critical in ensuring regulatory compliance, coordinating cross-functional activities, and managing end-to-end regulatory filings with Indian health authorities.

The position is ideal for regulatory professionals with strong expertise in CMC, clinical trial documentation, bioequivalence studies, and SUGAM portal submissions.


Key Responsibilities

  • Evaluate and develop regulatory strategies for pharmaceutical products intended for registration in India

  • Coordinate with cross-functional teams to obtain documentation required for regulatory submissions

  • Review and assess CMC (Chemistry, Manufacturing & Controls) documents in line with Indian regulatory guidelines

  • Review specifications for bulk drugs and finished formulations as per regulatory expectations

  • Review clinical trial and bioequivalence study documents for regulatory applications

  • Conduct scientific literature searches using relevant databases and regulatory sources

  • Prepare safety and efficacy rationales for new drugs and Fixed Dose Combinations (FDCs) based on published literature

  • Prepare executive summaries for SEC (Subject Expert Committee) referrals for drugs not approved in India

  • Compile and finalize CMC, Clinical Trial, and BE documents for dossier submission

  • File ND / SND / FDC applications on the SUGAM portal for domestic manufacturing, marketing, and clinical trial permissions

  • Review draft labels, cartons, and specimen artwork for regulatory compliance

  • Prepare prescribing information by referencing approved international prescribing information


Educational Qualifications

  • Master’s Degree in Pharmacy (M.Pharm) – Mandatory


Experience Required

  • 8 to 10 years of relevant experience in India Regulatory Affairs within the pharmaceutical industry

  • Proven hands-on experience in regulatory submissions, dossier compilation, and SUGAM portal filings

  • Strong understanding of Indian regulatory guidelines, CDSCO requirements, and approval processes


Travel Requirement

  • Not Applicable


Why Join Sun Pharma

At Sun Pharma, your growth, success, and well-being matter. We offer a dynamic work environment, opportunities for professional advancement, and the chance to contribute to impactful healthcare solutions. Join a globally respected organization where collaboration, accountability, and excellence drive everything we do.


Disclaimer

The above job description outlines the general nature and level of work expected for this role. It is not intended to be an exhaustive list of responsibilities, duties, or qualifications. Sun Pharmaceutical Industries Ltd reserves the right to modify job responsibilities or assign additional duties based on business needs and individual capabilities.