About Intas
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Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world.Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare.At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company’s growth and advancements in global healthcare.Job Title: Executive/Sr. Executive - Quality Assurance (IPQA)Job Requisitions No.: 15108Roles and Responsibilites
- In process Quality Assurance activity in Production and warehouse area 2. Provide line clearance as per SOP 3. Monitoring and QA rounds in production and Warehouse 4. Sample verification against TRF / BPCR 5. Carry out Semi-finished / finished product sampling for release, stability study and control samples 6. To send samples along with TRF to Quality control laboratory 7. Participate in media fill, process validation, cleaning validation activities as per requirement 8. Timely communication and co-ordination with all the stake holders 9. Participation in Change control, Deviation & Investigations as per requirement 10. Preparation / review of documents like; SOPs, risk assessment report and any other document as per requirement 11. Timely review of Batch Process & Control Records, Validation protocol / reports, Calibration, Qualification protocol / reports & Trend analysis data 12. Timely review of executed batch records and associated data 13. Keep vigilance on production operations 14. Review of Analytical Reports as per requirements 15. Participation in Audits & Compliance activity 16. In addition of above, any other responsibility assigned by Superior / HOD 17. Final release of critical intermediate and drug substance batches in LIMS and SAP 18. Risk assessment preparation and review 19. Draft MFR/BPCR/BPR review
Qualification RequiredB. Pharm / M. Pharm
Relevant Skills / Industry Experience
2-10 Years with Injectables or Biotech Induastry in IPQA departmentLocation:Plasma Fractionation Unit, Ahm, GJ, IN, 382210Travel: 0%Life at Intas PharmaceuticalsFor over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape.Date: 26 Aug 2025
