Principal Scientist - DPD

Job Description

About Intas 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: Principal Scientist - DPD Job Requisitions No.: 13704 Job Description Purpose of Job To lead (2-3 projects) and execute various drug product development studies for those projects. To build a strong process and formulation development related expertise in the group. To prepare stability protocols, compile data, prepare trend analysis and stability reports for a given project. Skill Required Formulation development, DP process development, Global filing and scientifically addressing regulatory queries, Analytical skills (HPLC and CE) Roles and Responsibilites Preparation of scientific justifications for regulatory queries for various markets 2. Prepare and/or review protocols and reports for various activities including formulation and stability 3. To conduct pre-formulation studies and formulation development 4. To conduct Technology transfer and support in process validation batches 5. Response to QA observations and closure of reports 6. Preparing and updating of SOP’s. Ensuring the calibration & PV of the equipment as per the schedules 7. Ensure completion of the work as per the project timelines and priorities 8. Take up additional lab responsibilities such as instrument maintenance 9. Review of LNBs, Raw data and study report to ensure integrity 10. To bring in more scientific depth to studies conducted and reports written 11. Any other responsibility assigned by the supervisor 12. Stability data evaluation and trend analysis for various projects 13. Working as department training coordinator for activities related to training management. Competencies Qualification Required M Pharma and PhD 8-12 years of Industry experience Relevant Skills / Industry Experience 8-12 years of Industry experience in formulation department Relevant professional / Educational background M Pharma & Phd Any Other Requirements (If Any) Compensation / Reward Location: Biotech, Ahmedabad, GJ, IN, 382213 Travel: 0% - 25% Life at Intas Pharmaceuticals For 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: 20 May 2025 Show more Show less