Pharma Jobs in Syngene: Hiring for the Role Senior Research Associate in Bangalore – Apply Now
Syngene International Ltd., a global leader in integrated scientific services, is hiring a Senior Research Associate in Bangalore. This role focuses on analytical R&D and GMP testing, including stability programs, method validation, and chromatographic analysis. Ideal for M.Sc. or M.Pharm graduates, this position offers hands-on experience in a cGMP-regulated environment supporting world-class pharmaceutical clients and cutting-edge scientific projects. If you are currently looking for Pharma Jobs in Syngene, this opportunity is for you.
Job Details:
- Job Title: Senior Research Associate (9-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 the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries. Syngene works with world leaders like Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. With a strong team of over 4,200 scientists, Syngene drives innovation, improves R&D productivity, and accelerates time-to-market for clients worldwide.
Educational Qualifications:
M.Sc. in Chemistry or M. Pharm for 9-II level.
Experience:
3–5 years with M.Sc. or 1–2 years with M. Pharm in analytical R&D or GMP environment.
Key Responsibilities:
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Test drug substance and drug product samples for release and stability using chromatographic, dissolution, and wet analytical techniques under GMP.
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Analyze API clinical campaign samples manufactured in Syngene pilot plant.
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Qualification or requalification of API reference standards.
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Perform instrument calibration and qualification.
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Conduct method validation and method transfers.
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Troubleshoot HPLC, dissolution apparatus, and other analytical instruments.
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Deliver analytical results within established timelines and applicable guidelines.
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Ensure compliance with quality systems and cGMP practices.
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Follow EHS requirements to maintain lab/plant safety.
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Document all work in electronic lab notebooks.
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Perform miscellaneous lab responsibilities as assigned.
Technical/Functional Skills:
- Strong background in analytical chemistry and laboratory practices.
- Proficiency in analytical techniques, instrument calibration, qualification, method validation, and testing.
- Knowledge of documentation as per GxP requirements, including electronic lab notebooks.
- Experience in stability testing and understanding of ICH guidelines & cGMP regulations.
- Exposure to cGMP-regulated environments; familiarity with regulatory inspections like US FDA, MHRA preferred.
- Proficiency in MS Office tools.
Behavioral Skills:
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Strong work commitment with enthusiasm and motivation.
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Excellent communication skills (speaking, listening, writing) and attention to detail.
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Proactive self-starter, able to work in dynamic, team-oriented environments.
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Flexible for shift-based work.
