We are looking for an experienced QC Analytical professional (6–12 years) with strong 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)
🏢 Enzene Biosciences
📍 Pune