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    Syngene Hiring Senior Analyst | Bangalore | Apply Now

    Senior Analyst Job At Syngene

    Syngene International Ltd is hiring a Senior Analyst – Stability and eGMP in Bangalore for its Early Phase GMP division. This Analyst Job role is ideal for analytical professionals with strong expertise in GMP laboratories, method validation, stability studies, and advanced analytical techniques within a global CRO/CDMO environment. Graduates seeking M Pharma jobs and want to start their career with Syngene careers can apply now.

    Job Details

    • Job Title: Senior Analyst – Stability & eGMP
    • Location: Bangalore, Karnataka, India

    About the Company

    Syngene International Ltd, incorporated in 1993, is a global discovery, development, and manufacturing organization serving pharmaceutical, biotechnology, nutrition, animal health, and specialty chemical industries. With over 4,000 scientists and partnerships with global leaders such as BMS, Amgen, GSK, and Baxter, Syngene is recognized for innovation-driven scientific excellence.

    Educational Requirements for Analyst Job Role

    • M.Pharm

    Key Responsibilities

    • Perform chromatographic and non-chromatographic analysis of APIs, drug products, intermediates, excipients, RM, PM, and finished products.
    • Execute analytical testing as per approved specifications, protocols, and procedures.
    • Interpret analytical data, report results, and complete documentation within defined timelines.
    • Record observations and data in logbooks, LIMS, ELN, and observation sheets.
    • Supporting stability summary reports and review final analytical documents is required for this Analyst Job role.
    • Handle deviations, investigations, and timely escalation to QA and department leadership.
    • Perform analytical method validation, method transfer, and support multiple client projects.
    • Conduct instrument calibration, preventive maintenance, and troubleshooting activities.
    • Participate in client and regulatory audits while ensuring cGMP and GDP compliance.
    • Prepare certificates of analysis, validation reports, and method transfer documents.
    • Support qualification and calibration of laboratory instruments and equipment.
    • Ensure safety compliance, PPE usage, and adherence to EHSS requirements.

    Skills Required for Analyst Job Role

    • Strong expertise in HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, and TGA
    • Knowledge of Chromeleon data management systems and LIMS
    • Understanding of cGMP, GDP, data integrity, and laboratory compliance
    • Good documentation and analytical interpretation skills
    • Effective communication and coordination abilities
    • Strong time management and organizational skills
    • Adaptive learning mindset

    Why This Analyst Job Role?

    • Opportunity to work with a globally recognized CRO/CDMO.
    • Exposure to advanced analytical technologies and early-phase GMP projects.
    • Hands-on involvement in stability studies, method validation, and regulatory audits.
    • Collaborative work environment with global pharmaceutical clients.
    • Strong platform for long-term growth in analytical and GMP careers.
    • Graduates seeking M Pharma jobs and want to start their career with Syngene careers can apply now.

    CLICK HERE TO APPLY ONLINE

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