Associate Scientist Jobs in Syngene: Hiring in Bangalore – Apply Now
If you are passionately looking for Associate Scientist Jobs in Syngene to build your career, here is an opportunity. Syngene International Ltd. is hiring an Associate Scientist in Bangalore to work on Analytical GMP Testing (AGT) and Syngene BMS Laboratory (SBL) stability programs. This role involves routine stability testing, method validation, instrument calibration, and troubleshooting HPLC and dissolution apparatus in a cGMP-regulated environment. Ideal candidates have a strong background in analytical chemistry, hands-on experience with stability samples, and 3–11 years of relevant industry experience depending on the level.
Job Details:
- Job Title: Associate Scientist (8-I) / Senior Associate Scientist (8-II)
- Location: Bangalore, KA, IN, 560099
- Department: BBRC PD ARD – GMP
About Syngene:
Syngene International Ltd., incorporated in 1993, is a global discovery, development, and manufacturing organization providing integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Syngene collaborates with leading global clients such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. With over 4,240 passionate scientists, Syngene drives innovation, enhances R&D productivity, accelerates time-to-market, and lowers costs of innovation.
Educational Qualifications:
M.Sc. in Chemistry or M. Pharm
Experience:
-
8-I Level: 6–8 years with M.Sc. or 3–5 years with M. Pharm
-
8-II Level: 9–11 years with M.Sc. or 6–8 years with M. Pharm
Key Responsibilities:
- Routine testing of stability samples using chromatographic, dissolution, and wet analytical techniques under GMP.
- Perform instrument calibration, method validation, and method transfers.
- Troubleshoot HPLC and dissolution apparatus.
- Interpret stability data and perform results trending.
- Investigate OOS/OOT and other laboratory events.
- Deliver analytical results within established timelines and applicable guidelines.
- Ensure compliance with quality systems and cGMP practices.
- Follow EHS requirements to maintain lab/plant safety.
- Maintain electronic lab notebook documentation.
- Perform miscellaneous lab responsibilities as assigned.
Technical/Functional Skills:
- Strong background in analytical chemistry and laboratory practices.
- Knowledge of analytical techniques and stability sample analysis.
- Understanding of instrument calibration, method validation, and routine analysis.
- Familiarity with GxP documentation practices, including electronic lab notebooks.
- Proficiency in MS Office tools.
- Experience with stability sample testing, ICH guidelines, and cGMP regulatory requirements.
- Exposure to cGMP-regulated environments and regulatory inspections like US FDA, MHRA preferred.
Behavioral Skills:
- Strong commitment, dedication, enthusiasm, and motivation.
- Excellent communication skills (speaking, listening, writing) with attention to detail.
- Proactive self-starter with ability to work in a dynamic team environment.
- Flexible for shift-based work and ability to meet tight deadlines while prioritizing workloads.
