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Senior Executive- India Regulatory Affairs

Sun Pharma
Sun Pharma
8-10 years
preferred by company
10 Feb. 9, 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 Title: Manager II – India Regulatory Affairs & Business Continuity
Company: Sun Pharmaceutical Industries Ltd.
Business Unit: R&D1 – Regulatory Affairs
Location: Baroda (Vadodara), Gujarat, India
Work Site: Tandalja – R&D
Job Grade: G11A
Posting Date: February 1, 2026
Job Type: Full-Time


About Sun Pharmaceutical Industries Ltd.

Sun Pharmaceutical Industries Ltd. is India’s largest pharmaceutical company and a globally trusted leader in specialty generics and innovative medicines. With a strong commitment to research-driven growth, Sun Pharma fosters a culture that empowers professionals to take ownership of their careers, continuously improve, and collaborate across functions to deliver high-quality healthcare solutions worldwide.


Position Overview

The Senior Executive – India Regulatory Affairs (Manager II level) will play a critical role in developing and executing regulatory strategies for product registrations in India. This position supports business continuity by ensuring timely, compliant regulatory submissions and approvals in alignment with Indian regulatory requirements. The role involves close collaboration with cross-functional teams across R&D, Quality, Clinical, and Manufacturing.


Key Responsibilities

Regulatory Strategy and Submissions

  • Develop and evaluate regulatory strategies for pharmaceutical products intended for registration in India

  • Coordinate with cross-functional teams to obtain CMC, clinical, bioequivalence, and related documentation for regulatory filings

  • Compile and submit regulatory dossiers in compliance with Indian regulatory guidelines

Documentation Review and Compliance

  • Review CMC documents, including specifications for bulk drugs and finished formulations, in accordance with regulatory expectations

  • Review clinical trial and bioequivalence study documents for inclusion in regulatory applications

  • Evaluate draft labels, cartons, and specimen packaging for regulatory compliance

  • Prepare prescribing information by referencing approved international prescribing information

Regulatory Intelligence and Scientific Support

  • Conduct literature searches using regulatory and scientific databases to support application strategies

  • Prepare scientific rationales for safety and efficacy of new drugs and fixed-dose combinations (FDCs) based on published literature

  • Draft executive summaries for Subject Expert Committee (SEC) referrals for products not approved in India

Regulatory Filing and System Management

  • Compile finalized CMC, clinical trial, and bioequivalence documentation from internal stakeholders

  • Submit ND, SND, and FDC applications through the SUGAM portal for domestic manufacturing, marketing authorization, and clinical trial approvals

  • Ensure regulatory submissions are accurate, complete, and aligned with applicable timelines


Required Experience and Qualifications

  • Education: Master’s degree in Pharmacy (M.Pharm)

  • Experience: 8–10 years of hands-on experience in India Regulatory Affairs within the pharmaceutical industry

  • Strong understanding of Indian regulatory frameworks, CDSCO requirements, and submission pathways

  • Proven experience in dossier compilation, regulatory strategy development, and SUGAM portal submissions

  • Ability to work cross-functionally and manage multiple regulatory activities simultaneously

  • Strong analytical, documentation, and scientific writing skills


Why Join Sun Pharma

At Sun Pharma, employee growth and well-being are central to the organization’s success. The company offers a collaborative work environment, learning opportunities, and a culture that encourages accountability, innovation, and continuous improvement. Employees are empowered to build meaningful careers while contributing to the development of safe, effective, and accessible medicines.


Disclaimer

This job description outlines the general nature and level of responsibilities associated with this role. It is not intended to be an exhaustive list of duties, responsibilities, or qualifications. Sun Pharmaceutical Industries Ltd. reserves the right to modify job responsibilities in accordance with business needs.