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: Associate Scientist - DPDJob Requisitions No.: 15797CompetenciesIntas - Problem SolvingIntas - Action OrientedIntas - Dealing with AmbiguityIntas - Customer FocusIntas - Time ManagementPurpose of JobSkill RequiredRoles and Responsibilites
- To support in planning, executing, & performing various drug product development studies and bio-similarity studies.
- Writing protocols and reports for various drug product development studies
- To support in process and technology transfer related documentations.
- To support in executing the stability studies and preparing reports for same.
- Getting trained on batch manufacturing procedure for drug product and do related documentation.
- To get trained on HPLC and CE techniques and perform analysis of stability samples.
- Response to DQA observations and closure of reports.
- Preparing and updating of SOPs.
- Ensuring the calibration of the equipment as per the schedules.
- Attending necessary trainings and following compliance.
- To follow Good Documentation Practices and Data Integrity requirements during any GxP Operation and recording at site.
- To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed.
- To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to Job description.
Qualification Required
Relevant Skills / Industry Experience
Relevant professional / Educational background
Any Other Requirements (If Any)
Compensation / RewardLocation:Biotech, Ahmedabad, GJ, IN, 382213Travel: 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 Dec 2025
