[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 # Senior Executive- India Regulatory Affairs Baroda, IN Senior individual contributor 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-Senior-Executive-India-Regulatory-Affairs/49704244/) [OpenNash Jobs](https://jobs.opennash.com/) / [Sun Pharma Industries](https://jobs.opennash.com/companies/sun-pharma-industries/) / Senior Executive- India Regulatory Affairs ## Job description ### Job Title Manager II – India Regulatory and business Conitnuity Business Unit: R&D1 Regulatory Affairs Job Grade G11A 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.” ### Key Responsibilities To evaluate regulatory strategy for products to be registered in India. To co-ordinate with Cross Functional Team for getting various documents required for filing the product in India. Responsible for reviewing CMC documents to be submitted in dossier as per regulatory guidelines. To review specification for bulk drug and formulations as per regulatory expectation. Responsible for reviewing clinical trial and bioequivalence study documents to be submitted in regulatory applications. To search literature through various websites as per the application strategy. To prepare rationale on safety and efficacy of new drug/FDC by referring published literature. To prepare executive summary for SEC referral for drugs not approved in India. To get all final CMC/CT/BE final documents from cross functional team and compilation of dossier for regulatory submission. To file ND/SND/FDC application on SUGAM portal for getting domestic manufacturing and marketing permission / clinical trial permission etc. To review draft specimen or label and carton. To prepare prescribing information by referring international prescribing information. Travel Estimate NA ### Job Requirements Educational Qualification Graduate: Masters (M-Pharm) ### Experience Tenure: 8-10 years 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: Jul 17, 2026 - Last checked: Oct 18, 2026 - Listed for: 93 days - Location: Baroda, IN[Apply on Sun Pharma Industries’s careers site →](https://careers.sunpharma.com/job/Baroda-Senior-Executive-India-Regulatory-Affairs/49704244/) ## More jobs at Sun Pharma Industries ### [Exe (Regulatory Affairs)](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/5130012188b125594e51/) 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 ### [Government Affairs Executive](https://jobs.opennash.com/companies/sentry-insurance/jobs/755a6bcac294c49fe98b/) Sentry Insurance · Nashville, TN OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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