{"id":1222611,"url":"https://alion.io/job/sun-pharma-exe-regulatory-affairs","title":"Exe (Regulatory Affairs)","company":{"id":1808960,"name":"Sun Pharma","domain":"sunpharma.com","url":"https://alion.io/company/sun-pharma","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":null},"role":"Public Policy","role_family":"Public Policy","seniority":null,"employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Vadodara, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":30000,"max_usd":87000,"period":"year","method":null,"sample_n":451},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-25T02:00:00Z","employer_posted_date":"2026-09-25","last_verified_at":"2026-09-26T12:41:17Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Job Title:\n\nRegulatory and Business Continuity\n\nBusiness Unit:\n\nR&D1 Regulatory Affairs\n\nJob Grade\n\nG12A Executive\n\nLocation :\n\nBaroda\n\nAt 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.\nAre 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.”\nJob Description\nReview all data and documents related to product registrations for various health authorities. \nCompile registration dossiers for submission to various health authorities like - US-FDA, Health Canada, Europe, Australia/New Zealand, Japan and Israel.\nPrepare responses to deficiency letters received from various agencies.\nMaintain life-cycle / post approval changes for drug product registration dossiers. \nProvide regulatory support to cross functional departments.\nPrepare and submit scientific advice to various health authorities. \neCTD compilation, verification and submission through electronic gateway\nReview, preparation and submission of annual reports to US FDA\nReview, preparation and submission of post approval supplements to US FDA\nReviewing of the plant change control and established the variation strategy for submission \nReview of query response prepared and compiled by regulatory associates \nReview of all the documents received from stake holder for dossier compilation, Query response and Life cycle management\nAllocation of projects to regulatory associate & manage the team for all the regulatory submission activities \n\nTravel Estimate\n\nNA\n\nJob Requirements\n\nEducational Qualification\n\nM. Pharm\n\nExperience\n\nTenure: 4 - 8 Yrs.\n\nYour Success Matters to Us\nAt 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\n\nDisclaimer: 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).","description_format":"text","description_chars":2805,"description_truncated":false,"requirements":{"experience_years_min":null,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Prescription Drugs","Generic Drugs","OTC & Consumer Health Products","APIs & Drug Manufacturing"],"lifecycle":[{"event":"open","at":"2026-09-25T12:42:34Z"}],"liveness":{"score":86,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.86,"p_room":1,"age_days":1,"expected_fill_days":21,"reasons":["conf:2","win:early","comp:brand"],"computed_at":"2026-09-26T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/sun-pharma-exe-regulatory-affairs","json_url":"https://alion.io/job/sun-pharma-exe-regulatory-affairs.json","meta":{"generated_at":"2026-09-27T01:43:16Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","usage":{"tier":"crawler","counted_by":"address","units_charged":1,"used_today":1550,"day_limit":5000,"remaining_today":3450,"minute_limit":60,"resets_at":"2026-09-28T00:00:00Z"}}}