<ul><li>Supervise and perform chemical and instrumental analysis of raw materials, intermediates, and finished products.</li><li>Review test data, COAs, and analytical reports ensuring adherence to cGMP and pharmacopeial standards.</li><li>Lead method validation, verification, and transfer activities in collaboration with R&amp;D.</li><li>Ensure compliance with data integrity practices and laboratory documentation standards.</li><li>Monitor and maintain QC laboratory equipment calibration and qualification status.</li><li>Support OOS, OOT, and deviation investigations and implement corrective actions.</li><li>Oversee stability studies and evaluate results as per ICH guidelines.</li></ul>

QC Executive