<ul><li>Conduct analysis of raw materials, in-process samples, finished products, and stability samples as per approved procedures.</li><li>Perform method validation, transfer, and verification activities.</li><li>Review and approve test results, logbooks, and worksheets.</li><li>Handle deviations, out-of-specification (OOS) incidents, and CAPA documentation.</li><li>Prepare, revise, and review SOPs, test methods, and calibration protocols.</li><li>Participate in regulatory and internal audits (USFDA, MHRA, WHO, etc.).</li><li>Train junior analysts and support technical troubleshooting on the shop floor or in the lab.</li></ul>

Executive/Sr. Executive-Quality Control (QMS)