<ul><li>Perform routine and non-routine disintegration testing of pharmaceutical dosage forms as per SOPs and pharmacopoeial standards.</li><li>Operate, maintain, and calibrate disintegration test apparatus and related laboratory equipment.</li><li>Develop, validate, and troubleshoot disintegration methods for new or modified formulations.</li><li>Record, analyze, and interpret test results accurately, ensuring compliance with GMP/GLP.</li><li>Prepare analytical reports and highlight any deviations or out-of-specification (OOS) results.</li><li>Support stability studies and method transfer/technology transfer activities.</li><li>Ensure proper handling, storage, and documentation of reagents, standards, and samples.</li><li>Assist during audits, inspections, and QA/RA activities.</li><li>Train and guide junior QC staff on disintegration testing procedures and SOP adherence.</li></ul>

Officer/Sr. Officer-QC (DT)