We are looking for an experienced QC Analytical qualified (6–12 years) with solid exposure to analytical testing, data review, and GMP-compliant quality systems in a biopharmaceutical workplace. Key Responsibilities:
Review analytical data for DS, DP, stability, method validation, and method transfer samples.
Perform and review chromatographic and plate-based analytical techniques.
Manage reference standards, laboratory documentation, calibration activities, and inventory.
Handle investigations related to Deviations, OOS, OOT, CAPA, and Change Controls.
Support equipment qualification (IQ/OQ/PQ), analyst qualification, and training activities.
Ensure compliance with GMP, GLP, and GDP requirements.

Technical Expertise

Required
CEX-HPLC, SE-HPLC, RP-HPLC• ELISA, RT-PCR• Capillary Electrophoresis (Maurice System)• Analytical data review and laboratory documentation Qualification: M. Sc., M. Pharm, M. Tech (Biotech), or relevant Master's degree. Experience:6–12 years of hands-on experience in QC Analytical functions within the biopharmaceutical industry.

📌 Quality Control Analyst Pune (India)
🏢 Enzene Biosciences
📍 India