We are looking for an experienced QC Analytical qualified (3 - 9 years) with strong exposure to analytical testing, data review, and GMP-compliant quality systems in a biopharmaceutical environment.

Key Responsibilities

- In-process and product analysis of drug substances, drug products, stability samples, and protocol-based studies.
- Instrument calibration and maintenance for HPLC, UFLC, Maurice systems, plate readers, and basic QC instruments (pH meter, osmometer, etc.).
- Reference standard management including qualification and reconciliation activities.
- Preparation and review of QC documentation such as Specifications, STPs, SOPs, CoAs, MTPs, MVPs, MVRs, and MTRs.
- Conducting analyst qualification and training as part of routine training management.
- Initiation, investigation, and closure of change controls and CAPA within due timelines.
- Handling deviations, incidents, OOS,



and OOT investigations in compliance with procedures.
- Technical proficiency in CEX-HPLC, SE-HPLC, RP-HPLC, ELISA, RT-PCR, and Capillary Electrophoresis.
- Adherence to GMP, GLP, GDP, and Data Integrity practices in all QC operations.
- Collaboration with cross-functional teams, ensuring effective communication and teamwork.

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: 3 - 9 years of hands-on experience in QC Analytical functions within the biopharmaceutical industry.

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