[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Sun Pharma Industries jobs](https://jobs.opennash.com/companies/sun-pharma-industries/) · [Search jobs](/search/) Sun Pharma Industries · Baroda, IN # Exe (Regulatory Affairs) Baroda, IN Legal & Compliance Listed on Sun Pharma Industries’s official careers site. Listed as of October 18, 2026. Check that it is still open and apply there. [Apply on Sun Pharma Industries’s careers site →](https://careers.sunpharma.com/job/Baroda-Exe-%28Regulatory-Affairs%29/58316544/) [OpenNash Jobs](https://jobs.opennash.com/) / [Sun Pharma Industries](https://jobs.opennash.com/companies/sun-pharma-industries/) / Exe (Regulatory Affairs) ## Job description ### Job Title Regulatory and Business Continuity Business Unit: R&D1 Regulatory Affairs Job Grade G12A Executive Location: Baroda 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 Description Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various health authorities like – US-FDA, Health Canada, Europe, Australia/New Zealand, Japan and Israel. Prepare responses to deficiency letters received from various agencies. Maintain life-cycle / post approval changes for drug product registration dossiers. Provide regulatory support to cross functional departments. - Prepare and submit scientific advice to various health authorities. eCTD compilation, verification and submission through electronic gateway - Review, preparation and submission of annual reports to US FDA Review, preparation and submission of post approval supplements to US FDA Reviewing of the plant change control and established the variation strategy for submission - Review of query response prepared and compiled by regulatory associates - Review of all the documents received from stake holder for dossier compilation, Query response and Life cycle management Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities Travel Estimate NA ### Job Requirements Educational Qualification M. ### Pharm Experience Tenure 4 – 8 Yrs. Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. ### Let’s create a brighter future together Disclaimer The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s). ## At a glance - Posted by the employer: Not stated - First seen by OpenNash: Oct 11, 2026 - Last checked: Oct 18, 2026 - Listed for: 7 days - Location: Baroda, IN[Apply on Sun Pharma Industries’s careers site →](https://careers.sunpharma.com/job/Baroda-Exe-%28Regulatory-Affairs%29/58316544/) ## More jobs at Sun Pharma Industries ### [Senior Executive- India Regulatory Affairs](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/b8ae70e2ae88d4a29c35/) Baroda, IN ### [Executive](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/37b04177d9c8d92432db/) Baroda, IN ### [Executive - API R&D](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/3c7eb32875b42b213fe5/) Baroda, IN ### [Executive - Analytical Development](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/18171d199d66c22575ca/) Baroda, IN ### [Executive - Biotechnology](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/9e4e12a6f20ea804ea9c/) Baroda, IN ## Similar jobs at other companies ### [Principal Regulatory Affairs Specialist](https://jobs.opennash.com/companies/cardinal-health/jobs/33905438205fffb92ba7/) Cardinal Health · International ### [Global Regulatory Affairs Manager, Oncology](https://jobs.opennash.com/companies/gsk/jobs/09fdd8d7e12226e3ad65/) GSK · Rockville, Maryland, United States of America ### [Director, Global Regulatory Affairs (GRL)](https://jobs.opennash.com/companies/daiichi-sankyo/jobs/23bdbd6a298974011fee/) Daiichi Sankyo · Basking Ridge, NJ, USA ### [Director, Regulatory Affairs, Companion Diagnostics](https://jobs.opennash.com/companies/daiichi-sankyo/jobs/fdf9cbaa775b4385105d/) Daiichi Sankyo · Basking Ridge, NJ, USA ### [Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs](https://jobs.opennash.com/companies/viatris/jobs/736e7dfaffb1fb1dc513/) Viatris · Washington, District of Columbia, USA OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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