<ul><li>Perform analytical method development and validation for pharmaceutical products.</li><li>Operate analytical instruments such as HPLC, GC, UV, IR, and dissolution apparatus.</li><li>Prepare and review analytical reports, test protocols, and method documentation.</li><li>Conduct stability studies and forced degradation experiments as per ICH guidelines.</li><li>Ensure compliance with cGMP, GLP, and data integrity standards during all activities.</li><li>Assist in method transfer to QC labs and manufacturing locations.</li><li>Analyze raw materials, intermediates, and finished products during development.</li><li>Maintain accurate lab records and ensure audit readiness.</li></ul>

ADL Executive (Routine Analysis)