Sun Pharma Hiring for Executive – Regulatory Affairs Role: RA jobs 2026

ByPharma Hiring Hub

Sun Pharmaceutical Industries Ltd, one of India’s leading global pharmaceutical companies, is hiring an Executive – Regulatory Affairs for its R&D division at the Vadodara (Baroda) location. This opportunity is well‑suited for professionals with 1–4 years of experience in regulatory submissions, CMC documentation, and product lifecycle management.

The role focuses on supporting global and MENA market submissions, including dossier preparation, response to regulatory deficiencies, and coordination with cross‑functional teams. Candidates will gain hands‑on exposure to regulatory strategy execution, compliance with international guidelines, and end‑to‑end RA activities within a regulated global environment.

This position is ideal for candidates targeting Regulatory Affairs jobs in India (2026) and looking to strengthen their expertise in global regulatory operations and dossier management.

Regulatory affair jobs

Job Overview

  • Position: Executive – Regulatory Affairs
  • Department: Regulatory affairs
  • Location: Vadodara, India
  • Experience: 1-4 Years
  • Qualification: M.Pharm
  • Job Type: Full-Time
  • Last Date to apply: 31 March 2026

Key Responsibilities – Executive – Regulatory Affairs

  • New Submissions & Renewals
    • Review and prepare CMC (Chemistry, Manufacturing & Controls) dossiers for new submissions and renewals.
    • Review development reports, scale‑up reports, specifications, stability protocols, and artworks to ensure adequacy prior to Exhibit batch initiation.
  • Regulatory Approvals & Deficiency Handling
    • Review regulatory queries and prepare responses to deficiencies to support timely product approvals by regulatory authorities.
  • Lifecycle Management – Drug Formulations
    • Prepare and review variations as per country‑specific regulatory requirements, supporting changes such as:
      • API vendor changes
      • Changes in ROS or test parameters
      • Drug product manufacturing site changes
      • Product harmonization activities
  • Regulatory Compliance & Documentation
    • Prepare, review, and circulate approval packages along with product history sheets to relevant stakeholders.
    • Update documentation based on regulatory queries and post‑approval variations.
    • Ensure proper archival of complete product information within the central regulatory repository.
  • Impact Assessment & Change Control
    • Review and assess regulatory filing impact related to variations, change controls, and lifecycle updates to ensure continued compliance with global regulatory requirements.

Required Skills & Qualifications

  • Educational Background: Master degree in a scientific discipline or healthcare field is preferred.
  • Regulatory Knowledge: Good working knowledge of regulatory requirements, including GCP and ICH guidelines.
  • Therapeutic & Protocol Knowledge:Understanding of therapeutic areas and study protocols as provided through company training.
  • Technical Skills: Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Communication Skills:Strong written and verbal communication skills with a good command of the English language.
  • Organizational & Problem‑Solving Skills: Effective organizational, planning, and problem‑solving abilities to manage multiple study tasks.
  • Time & Financial Management:Capable of managing time, priorities, and site‑level financial activities efficiently.
  • Professional Relationships: Ability to establish and maintain effective working relationships with study sites, coworkers, managers, and clients.

Why Join Sun Pharma?

  • Global Pharmaceutical Leader
  • Be part of one of India’s largest and most respected pharmaceutical companies, with a strong presence across regulated and emerging markets worldwide.
  • Strong Regulatory Affairs Exposure
  • Gain hands‑on experience across global and MENA regulatory submissions, CMC documentation, deficiency handling, and lifecycle management within a highly regulated environment.
  • End‑to‑End R&D Regulatory Role
  • Work closely with R&D, manufacturing, quality, and supply‑chain teams, supporting regulatory strategy from development through approval and post‑approval changes.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ– Executive – Regulatory Affairs

1. Who can apply for the Executive – Regulatory Affairs role at Sun Pharma?

Candidates with 1–4 years of experience in regulatory submissions, CMC documentation, and lifecycle management within the pharmaceutical industry.

2. What educational background is required for this role?

Typically, candidates hold a degree in Pharmacy, Pharmaceutical Sciences, or a related life sciences discipline.

3. What type of regulatory work will I handle in this role?

You will support CMC dossier preparation, regulatory submissions, deficiency responses, variations, renewals, and post‑approval lifecycle management activities.

4. Which markets will this role primarily support?

The role focuses on MENA and global markets, offering exposure to international regulatory requirements and submission strategies.

5. Will I be involved in lifecycle management activities?

Yes. You will prepare and review variations, handle change controls (API changes, site changes, test parameter updates), and support ongoing product compliance.

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