<ul><li>Conduct analysis of raw materials, intermediates, and finished products as per SOPs and pharmacopeia.</li><li>Operate and maintain lab instruments including HPLC, GC, UV, and FTIR.</li><li>Prepare and review test records, COAs, and analytical reports.</li><li>Perform method validation, transfer, and stability studies as required.</li><li>Handle OOS/OOT results and assist with deviation investigations.</li><li>Ensure compliance with GLP, cGMP, and regulatory standards during QC operations.</li><li>Maintain laboratory documentation, logbooks, and calibration records.</li><li>Follow safety protocols and ensure proper waste disposal practices.</li></ul>

QC Executive