Sun Pharma Hiring for Executive – Regulatory Affairs Role: RA jobs 2026
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.
🏢 About the Organization
Sun Pharmaceutical Industries Ltd. is one of India’s leading global pharmaceutical companies, with a strong presence across branded generics, specialty medicines, and complex therapies. The company operates under stringent regulatory frameworks and adheres to global quality and compliance standards. Working at Sun Pharma provides exposure to global regulatory practices, structured development programs, and cross‑functional collaboration.
📊 Role Summary
- 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
📋 Responsibilities Overview – 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
- Prepare and review variations as per country‑specific regulatory requirements, supporting changes such as:
- 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.
🎓 Qualification Criteria
- Educational Background:
- Master’s degree in a scientific discipline or healthcare field is preferred
- Experience:
- 1 to 4 years of relevant experience in Regulatory Affairs or related functions
- Experience working in regulated pharmaceutical or clinical environments is preferred
🧠 Required Competencies
- Good working knowledge of:
- Good Clinical Practice (GCP)
- ICH guidelines
- Understanding of regulatory processes and documentation standards
- Ability to apply protocol knowledge as provided through company training
- Understanding of therapeutic areas and study protocols
⭐ Work Insight
The Executive – Regulatory Affairs role is crucial in ensuring that clinical and development activities meet regulatory and ethical standards. Professionals in this role act as a bridge between development teams and regulatory requirements. Working at Sun Pharma provides hands‑on exposure to global compliance standards and regulatory systems, making it an important step toward senior regulatory positions.
🎯 Target Candidates
This opportunity is suitable for:
- Regulatory professionals with 1–4 years of experience
- Candidates with knowledge of GCP and ICH guidelines
- Life sciences or healthcare graduates seeking regulatory career growth
- Professionals interested in global pharma regulatory exposure
📈 Career Development
With experience and consistent performance, professionals can progress into roles such as:
- Senior Executive – Regulatory Affairs
- Regulatory Affairs Manager
- Clinical Regulatory Specialist
- Global Regulatory Operations roles
Sun Pharma supports professional development and long‑term career growth.
💰 Salary Overview
The salary package for this position is aligned with industry standards and varies based on experience and expertise.
Compensation will be competitive and based on qualifications, skills, and relevant experience.
💡 Expert Guidance
- Revise GCP and ICH guideline fundamentals
- Strengthen understanding of regulatory documentation workflows
- Be prepared to discuss regulatory experience and compliance scenarios
- Highlight attention to detail and cross‑functional coordination skills
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
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.
