Quality Control Analyst

We are looking for an experienced QC Analytical professional (612 years) with strong exposure to analytical testing, data review, and GMP-compliant quality systems in a biopharmaceutical environment.

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:

612 years of hands-on experience in QC Analytical functions within the biopharmaceutical industry.