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Senior Executive- India Regulatory Affairs

Sun Pharma
Sun Pharma
8-10 years
Not Disclosed
10 Jan. 9, 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

Job Title: Senior Executive – India Regulatory Affairs (Manager II)
Company: Sun Pharmaceutical Industries Ltd
Business Unit: R&D – Regulatory Affairs
Job Grade: G11A
Location: Tandalja, Baroda, Gujarat, India
Posted Date: January 3, 2026

Company Overview:
Sun Pharma empowers employees to “Create Your Own Sunshine” by fostering a collaborative, growth-oriented, and supportive environment. With a global presence in pharmaceuticals, Sun Pharma encourages professionals to take charge of their careers, continuously improve, and contribute meaningfully to healthcare and drug development in India.

Position Overview:
Sun Pharma is seeking a highly experienced Senior Executive – India Regulatory Affairs with 8–10 years of experience in regulatory affairs, drug registration, and dossier preparation. The candidate will play a key role in managing regulatory submissions, reviewing CMC, clinical, and BE documents, and ensuring timely approvals for new drugs, fixed-dose combinations (FDCs), and clinical trial applications in India.

Key Responsibilities:

  • Evaluate regulatory strategies for new drugs, generics, and FDCs for registration in India.

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

  • Review Chemistry, Manufacturing, and Controls (CMC) documents for regulatory submissions.

  • Review bulk drug and formulation specifications in compliance with regulatory expectations.

  • Assess clinical trial and bioequivalence (BE) study documents for submission.

  • Conduct literature searches to support regulatory applications and prepare rationale on drug safety and efficacy.

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

  • Compile final CMC, clinical trial (CT), and BE documents into comprehensive dossiers for submission.

  • File ND/SND/FDC applications via the SUGAM portal for domestic manufacturing, marketing permission, and clinical trial approvals.

  • Review draft labels and cartons, and prepare prescribing information based on international references.

Educational Requirements:

  • Master’s degree in Pharmacy (M. Pharm) or equivalent.

Experience Requirements:

  • 8–10 years of relevant experience in regulatory affairs, dossier preparation, and regulatory submissions in India.

Why Join Sun Pharma:
Sun Pharma values your growth, well-being, and career development. Employees benefit from professional development opportunities, a collaborative work culture, and robust support to achieve career milestones. Join Sun Pharma to contribute to regulatory excellence and play a pivotal role in bringing safe and effective medicines to the Indian market.

Apply Today:
If you are experienced in regulatory strategy, dossier preparation, and Indian drug regulations, apply now to join Sun Pharma as a Senior Executive – India Regulatory Affairs in Baroda.