Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Executive - Regulatory Affairs

Sun Pharma
Sun Pharma
1-4 years
preferred by company
10 Feb. 11, 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

Location: Tandalja, R&D, Baroda, Gujarat, India
Company: Sun Pharmaceutical Industries Ltd
Date Posted: January 20, 2026
Employment Type: Full-Time
Business Unit: R&D – Regulatory Affairs
Job Grade: G12A
Industry: Pharmaceuticals | Regulatory Affairs | Drug Lifecycle Management


About Sun Pharma

Sun Pharmaceutical Industries Ltd. is a global leader in the pharmaceutical industry, committed to improving healthcare outcomes worldwide. With a strong presence across emerging and developed markets, Sun Pharma develops, manufactures, and markets high-quality generic, branded, and specialty pharmaceutical products. Our culture empowers employees to take charge, thrive collaboratively, and continuously grow in a supportive, innovative environment.

Learn more: www.sunpharma.com


Job Summary

The Executive – Regulatory Affairs will manage regulatory submissions, renewals, variations, and lifecycle management for pharmaceutical products in MENA and South African markets. The role involves preparing high-quality CMC dossiers, responding to regulatory queries, and ensuring compliance with country-specific requirements, supporting timely product approvals.


Experience Required

  • 1–4 years of experience in regulatory affairs, preferably in pharmaceutical R&D or lifecycle management

  • Hands-on experience with CMC dossier preparation, regulatory submissions, and product lifecycle updates


Educational Qualification

  • Graduate/Postgraduate: M.Sc. / M.Pharm in Pharmaceutical Sciences, Chemistry, or related discipline


Key Responsibilities

Regulatory Submissions & Approvals

  • Prepare, review, and submit CMC dossiers for new products, renewals, and variations

  • Review development reports, scale-up reports, specifications, stability protocols, and artworks prior to Exhibit batch initiation

  • Respond to regulatory deficiency queries to enable product approvals

Lifecycle Management

  • Manage variations and product updates including API vendor changes, formulation site changes, test parameter updates, and product harmonization

  • Ensure timely documentation and update of approvals in central repositories and regulatory filing systems

Regulatory Compliance & Documentation

  • Circulate approval packages and maintain comprehensive product information for stakeholders

  • Evaluate the impact of regulatory filings, change controls, and variations on product lifecycle

  • Maintain up-to-date knowledge of regional regulatory requirements for South Africa and MENA markets

Collaboration & Stakeholder Engagement

  • Work closely with cross-functional teams including R&D, QA, Manufacturing, and Business Units

  • Ensure regulatory compliance and facilitate timely communication with stakeholders for approvals


Required Skills & Competencies

  • Knowledge of global regulatory requirements and CMC guidelines

  • Strong understanding of drug development lifecycle and pharmaceutical regulations

  • Proficiency in document management systems, MS Office, and regulatory submission tools

  • Excellent communication, analytical, and organizational skills

  • Ability to prioritize tasks, manage deadlines, and ensure high-quality deliverables


Travel Requirements

  • Not applicable for this role


Why Join Sun Pharma?

  • Opportunity to work on regulatory submissions and lifecycle management for global pharmaceutical products

  • Gain exposure to MENA and South African regulatory frameworks

  • Be part of a collaborative, growth-oriented, and innovative work culture

  • Contribute to timely product approvals and compliance excellence in a leading pharmaceutical company


Disclaimer

This job description is designed to indicate the general nature and level of work performed by employees within this classification. It is not a comprehensive inventory of all duties, responsibilities, and qualifications. Sun Pharma reserves the right to modify duties or assign comparable responsibilities based on organizational needs.