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Senior Executive- India Regulatory Affairs

Sun Pharma
Sun Pharma
8-10 years
Not Disclosed
10 Jan. 20, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Company: Sun Pharmaceutical Industries Ltd
Business Unit: R&D – Regulatory Affairs
Location: Baroda, Gujarat, India
Job Type: Full-Time
Experience Required: 8–10 Years
Posted Date: January 3, 2026


Job Overview

Sun Pharma is seeking a Senior Executive / Manager II – India Regulatory Affairs to lead regulatory strategy, filings, and compliance for pharmaceutical products in India. This role is ideal for experienced regulatory professionals with deep knowledge of drug registration, CMC documentation, clinical trials, and bioequivalence studies.

The candidate will work closely with cross-functional teams to compile dossiers, ensure regulatory compliance, and support domestic product approvals while maintaining high standards of quality and safety.


Key Responsibilities

Regulatory Strategy & Dossier Management

  • Evaluate regulatory strategies for the registration of pharmaceutical products in India

  • Compile and review CMC, clinical trial (CT), and bioequivalence (BE) study documents for regulatory submissions

  • Prepare rationale on safety and efficacy of new drugs or fixed-dose combinations (FDCs) based on published literature

  • Prepare executive summaries for SEC referrals for drugs not yet approved in India

  • Coordinate with cross-functional teams to gather all necessary documents for dossier compilation and submission

Regulatory Filings & Compliance

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

  • Review draft specimen labels, cartons, and prescribing information ensuring compliance with Indian regulations and international standards

  • Maintain up-to-date knowledge of regulatory requirements and guidelines issued by CDSCO and other authorities

Cross-Functional Collaboration

  • Liaise with internal stakeholders including R&D, Quality, Clinical, and Regulatory teams

  • Support document finalization for submission to regulatory authorities

  • Ensure timely and accurate completion of all regulatory tasks aligned with business priorities


Job Requirements

Educational Qualification

  • Master’s degree in Pharmacy (M.Pharm) or relevant life science discipline

Experience

  • 8–10 years of professional experience in regulatory affairs in the pharmaceutical industry

  • Expertise in Indian regulatory submissions, CMC documentation, clinical trial and BE study filings

Skills & Competencies

  • Strong knowledge of CDSCO guidelines, drug registration, and clinical trial regulations in India

  • Excellent analytical and documentation skills

  • Ability to coordinate with cross-functional teams effectively

  • High attention to detail, problem-solving skills, and ability to meet tight deadlines

  • Proficient in preparing regulatory dossiers and reviewing scientific documents