[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 · Dadra, IN # Senior Executive - Production (Qualification & Validation) Dadra, IN Senior individual contributor Manufacturing & Production 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/Dadra-Senior-Executive-Production-%28Qualification-&-Validation%29/55823944/) [OpenNash Jobs](https://jobs.opennash.com/) / [Sun Pharma Industries](https://jobs.opennash.com/companies/sun-pharma-industries/) / Senior Executive - Production (Qualification & Validation) ## Job description ### Job Purpose To support and execute qualification and validation activities related to production equipment, utilities, and processes in an Oral Solid Dosage (OSD) manufacturing facility, ensuring compliance with USFDA, cGMP, and regulatory requirements. ### Key Responsibilities Qualification & Validation Activities - Execute and support qualification of: Equipment (DQ, IQ, OQ, PQ) Utilities (HVAC, purified water, compressed air, etc.) Production areas and systems - Perform process validation activities for OSD products including: Prospective, concurrent, and re‑validation studies - Prepare, review, and execute validation protocols and reports as per approved SOPs. Ensure validation activities are completed within defined timelines. Production Support Coordinate with Production, Engineering, QA, and QC teams during qualification and validation activities. Support scale‑up, technology transfer, and new product introduction from a validation perspective. Ensure adherence to approved BMRs, SOPs, and validation protocols during execution. Assist in troubleshooting process or equipment‑related issues during validation batches. Documentation & Compliance Prepare and maintain validation documentation in compliance with: USFDA cGMP ICH guidelines (Q8, Q9, Q10) Ensure data integrity and compliance with ALCOA+ principles. Maintain proper documentation, logs, and records for audits and inspections. Support regulatory inspections, internal audits, and customer audits related to validation. Continuous Improvement Participate in risk assessments (FMEA, risk analysis) related to validation activities. Support change control evaluations and impact assessments. Contribute to continuous improvement initiatives in production and validation processes. Educational Qualification Bachelor’s degree in: Pharmacy (B.Pharm / M.Pharm) ### Experience 6–8 years of experience in: Production / Qualification / Validation USFDA‑approved OSD pharmaceutical manufacturing plant Hands‑on experience with equipment qualification and process validation is essential. Technical Skills & Knowledge Strong understanding of: cGMP requirements USFDA regulatory expectations OSD manufacturing processes Knowledge of validation lifecycle concepts. Familiarity with production equipment such as: Blenders, granulators, compression machines, coating machines Good documentation and technical writing skills. Working knowledge of QMS, deviation, CAPA, and change control systems. ### Behavioral & Soft Skills - Strong attention to detail Good analytical and problem‑solving skills Effective communication and coordination abilities - Ability to work in cross‑functional teams Compliance‑oriented and quality‑focused mindset Preferred / Added Advantage Exposure to regulatory audits (USFDA, MHRA, WHO, etc.) Experience in validation of new equipment or facility expansion - Knowledge of cleaning validation (basic level) ## 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: Dadra, IN[Apply on Sun Pharma Industries’s careers site →](https://careers.sunpharma.com/job/Dadra-Senior-Executive-Production-%28Qualification-&-Validation%29/55823944/) ## More jobs at Sun Pharma Industries ### [Sr Executive - Production QMS](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/3becf2131d507b4770a4/) Dadra, IN ### [Engineering CSV & QMS Manger](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/9c42793cab81d784ae17/) Dadra, IN ### [Senior Executive - Warehouse & Dispatch](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/b73503263bd096478b31/) Dadra, IN ### [Senior Officer - Micro](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/285981bd4180959ec7d3/) Dadra, IN ### [Sr. Officer / Executive - MSTG](https://jobs.opennash.com/companies/sun-pharma-industries/jobs/0f4b471ce2fba057adbd/) Dadra, IN ## Similar jobs at other companies ### [Nuclear Qualification Coordinator](https://jobs.opennash.com/companies/abb/jobs/4cffa4cc7b70b96474aa/) ABB · Remote, United States of America ### [Lead Qualification Representative](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/e18796fbe6f30b7b45ad/) Thermo Fisher Scientific · Carlsbad, California, United States of America ### [Manager Machine Operator Qualification](https://jobs.opennash.com/companies/canadian-pacific-kansas-city/jobs/2148e50fb993363b782f/) Canadian Pacific Kansas City · USA ### [Sr. Scientist – Reference Standards Qualification](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/8ecc152acf10abc28ecf/) Thermo Fisher Scientific · Boston, Massachusetts, United States of America ### [Validation Engineer](https://jobs.opennash.com/companies/qualcomm/jobs/7980aacaf472ea146fcc/) Qualcomm · Tijuana, Baja California, Mexico OpenNash lists jobs from employers’ own careers sites and does not handle applications. Dates come from the employer where stated; “first seen” and “last checked” are our own observations. OpenNash Jobs · Official listings with dates and links to the employer. [Weekly hiring report](/reports/hiring/) · [Methodology](/methodology/)