Research Associate Jobs at Syngene | Chemistry Graduates Apply
Are you looking for Research Associate Jobs in Bangalore with a globally recognized pharmaceutical research organization? Syngene International Ltd. is hiring for Research Associate (9-I) and Senior Research Associate (9-II) roles in its GMP Analytical Research and Development division. This Syngene Careers opportunity is ideal for candidates seeking growth, hands-on analytical exposure, and stability in regulated research environments.
About Syngene
Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene’s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240-strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation. Choosing Syngene Jobs means building a long-term career in science, innovation, and global research excellence.
Job Description
- Designation: Research Associate (9-I) or Senior Research Associate (9-II)
- Job Location: Bangalore
- Department: BBRC PD ARD – GMP
- Division: Dedicated Centre
Job Purpose
Analytical
Research and Development working on Analytical GMP testing (AGT), and Syngene BMS Laboratory (SBL) stability programs.Key Responsibilities
- Testing of samples (drug substance and drug product for release testing and stability) using chromatographic, dissolution, and wet analytical techniques under a GMP environment, following cGMP practices
- Analysis of API clinical campaign samples manufactured in Syngene pilot plant
- Qualification or requalification of API reference standards
- Performing instrument calibration and qualification
- Performing method validation and method transfers
- Troubleshooting HPLC, dissolution apparatus, and other analytical instruments in the lab
- Deliver analytical results within the established windows and as per applicable guidelines
- Compliance & implementation of quality systems
- Follow environment, health, and safety (EHS) requirements at all times in the workplace, ensuring individual and lab/plant safety
- Electronic lab notebook documentation
- Miscellaneous lab responsibilities
Educational Qualifications
M.Sc. Chemistry for 9-I; M.Sc. Chemistry or M. Pharm for 9-II;
Technical/Functional Skills
- The candidate should have a good educational and theoretical, analytical chemistry background
- Good knowledge of analytical techniques
- The candidate should understand instrument calibration, qualification, method validation, and analytical testing.
- Good understanding of documentation as per GxP requirements (electronic notebook)
- The candidate should have good proficiency in MS Office tools
- Experience in stability samples testing and good knowledge of ICH guidelines & cGMP regulatory requirements
- Must have worked in a cGMP-regulated environment, exposure to regulatory inspections like US FDA, MHRA, etc., is preferred.
Behavioral Skills
- Strong commitment toward work and a high level of dedication, enthusiasm, and motivation
- Good speaking-listening-writing skills, attention to detail, proactive self-starter
- Ability to work successfully in a dynamic environment
- Should be able to work in a team and be flexible for working in shifts.
