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Executive - Regulatory Affairs

Sun Pharma
Sun Pharma
1-4 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

Executive – Regulatory Affairs

Company: Sun Pharmaceutical Industries Ltd.
Business Unit: R&D1 – Regulatory Affairs
Job Grade: G12A
Location: Baroda (Vadodara), Gujarat, India
Work Location: Tandalja – R&D
Posting Date: January 20, 2026
Employment Type: Full-Time


About Sun Pharmaceutical Industries Ltd.

Sun Pharmaceutical Industries Ltd. is a globally recognized pharmaceutical leader with a strong presence across specialty, generic, and innovative medicines. Driven by science and quality, Sun Pharma offers professionals a dynamic environment that supports continuous learning, cross-functional collaboration, and career growth within a globally compliant regulatory framework.


Role Overview

The Executive – Regulatory Affairs will support regulatory submissions, approvals, and lifecycle management activities for pharmaceutical products in international markets, with a primary focus on South Africa and selected MENA regions. The role involves preparation and review of quality (CMC) dossiers, management of regulatory variations, and coordination with internal stakeholders to ensure timely and compliant regulatory approvals.


Key Responsibilities

Regulatory Submissions and Renewals

  • Prepare and review Chemistry, Manufacturing, and Controls (CMC) dossiers for new product registrations and renewals

  • Review development reports, scale-up documents, specifications, stability protocols, and artworks prior to initiation of exhibit batches

  • Support timely submission of regulatory dossiers in line with country-specific regulatory requirements

Regulatory Approvals and Agency Queries

  • Review and prepare responses to regulatory deficiency letters to facilitate product approvals

  • Coordinate with cross-functional teams to address agency questions and resolve regulatory queries efficiently

Lifecycle Management and Variations

  • Prepare and review regulatory variations to support post-approval changes, including API vendor updates, manufacturing site changes, test parameter modifications, and product harmonization

  • Ensure lifecycle management activities comply with country-specific regulatory guidelines

Regulatory Compliance and Documentation

  • Prepare, review, and circulate approval packages, including product history sheets, to relevant stakeholders

  • Maintain and update comprehensive product documentation in central regulatory repositories

  • Assess regulatory impact of variations, change controls, and compliance-related updates


Geographic Scope

  • Primary Market Focus: South Africa

  • Supporting selected MENA markets as required


Required Experience and Qualifications

  • Education: M.Pharm or M.Sc in a relevant scientific discipline

  • Experience: 1–4 years of experience in Regulatory Affairs within the pharmaceutical industry

  • Hands-on experience with CMC documentation and regulatory submissions

  • Knowledge of international regulatory requirements, particularly for emerging and semi-regulated markets

  • Strong documentation, coordination, and regulatory compliance skills

  • Ability to manage multiple regulatory activities in a deadline-driven environment


Why Join Sun Pharma

Sun Pharma is committed to creating an environment where employees can grow professionally while contributing to global healthcare advancement. The organization offers continuous learning opportunities, exposure to international regulatory markets, and a culture that values accountability, collaboration, and scientific excellence.


Disclaimer

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