<ul><li>Perform testing and analysis of raw materials, intermediates, finished products, and stability samples.</li><li>Operate and maintain analytical instruments like HPLC, GC, UV, FTIR, Dissolution, etc.</li><li>Document test results, prepare COAs, and ensure compliance with cGMP and GLP standards.</li><li>Support method validation, method transfer, and stability studies as per protocols.</li><li>Handle OOS/OOT investigations and assist in CAPA implementation.</li><li>Ensure adherence to pharmacopeial guidelines (IP, USP, EP) and regulatory requirements.</li><li>Maintain laboratory records, logbooks, and ensure data integrity (ALCOA principles).</li><li>Participate in internal audits and regulatory inspections; ensure lab readiness.</li></ul>

Quality Control Executive (RM)