<ul><li>Plan, execute, and review analytical method validation and verification studies for raw materials, in-process, and finished products.</li><li>Develop validation protocols, method transfer documents, and ensure compliance with ICH, USP, and regulatory guidelines.</li><li>Supervise QC analysts in performing method validation, robustness, accuracy, precision, linearity, and specificity studies.</li><li>Review and approve validation reports, data, and related documentation for accuracy and compliance.</li><li>Ensure calibration, qualification, and proper maintenance of analytical instruments (HPLC, GC, UV, etc.).</li><li>Coordinate with QA, R&amp;D, and production teams for method development, technology transfer, and troubleshooting.</li><li>Ensure all validation activities comply with cGMP, GLP, and internal quality standards.</li></ul>

Asst. Manager-QC (Analytical Method Validation)