<ul><li>Perform routine analysis of raw materials, in-process, and finished products.</li><li>Operate and maintain laboratory instruments like HPLC, GC, UV, FTIR, etc.</li><li>Ensure testing complies with pharmacopeial standards (IP, USP, BP) and internal SOPs.</li><li>Document test results accurately in logbooks, worksheets, and reports as per cGMP/GLP.</li><li>Conduct method validations, stability testing, and calibration activities.</li><li>Investigate and report OOS (Out of Specification) and OOT (Out of Trend) results.</li><li>Monitor laboratory inventory and ensure availability of reagents and standards.</li><li>Coordinate with QA, production, and warehouse teams for sampling and release.</li></ul><p>&nbsp;</p>

QC Executive