Executive Jobs at Sun Pharma | MSc Chemistry Candidates Apply Now
Executive Jobs at Sun Pharma. Sun Pharmaceutical Industries Ltd has announced an opening for the role of Executive – Regulatory Affairs at its R&D centre in Baroda. This position offers an exciting opportunity to contribute to regulatory submissions, lifecycle management, and compliance activities for MENA markets. With a strong focus on quality dossier preparation, product approvals, and stakeholder coordination, this role is ideal for candidates looking to grow within a global pharmaceutical leader committed to innovation and professional development.
Company Overview
At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey, and thrive in a supportive community. Are you ready to create your own sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.
- Job Title: Executive – Regulatory Affairs
- Date: Nov 23, 2025
- Location: Tandalja – R&D, Baroda
- Company: Sun Pharmaceutical Industries Ltd
- Business Unit: R&D1 Regulatory Affairs
- Job Grade: G12A
- Location: Baroda
- Job Description
Regulatory submission of new products, renewals, variations, response to queries, and Lifecycle management for MENA markets through the preparation of quality dossiers enabling timely approvals.
Area of Responsibility
- New submissions/Renewals:
- Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.
- Review documents (Development report, scale-up report, specification, stability protocol), artworks, etc., before initiation of Exhibit batches for adequacy.
- Approval:
- Review & prepare responses to deficiency enabling approval of products filed to regulatory agency.
- Lifecycle management for drug formulations:
- Prepare and review variations as per the country-specific requirements to support approval of changes such as API vendor changes/changes in ROS/test parameters; DF site changes; harmonization of products, etc.
- Regulatory compliance:
- Prepare, review, and circulate the approval package with the product history sheet to stakeholders upon receipt of approval, and update the same based on queries and variations.
- Ensure reposition of comprehensive product information into the central repository.
- Review regulatory filing impact of variations, change controls, etc.
- Geographic Scope/Market: MENA-GCC, UAE, Oman, Saudi Arabia, Egypt, Iran, Iraq, Bahrain, etc.
- Travel Estimate: NA
Job Requirements
- Educational Qualification: Graduate: M.Sc / M.Pharm
- Experience: Tenure: 1-4 years
