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Perform stability testing on pharmaceutical products according to approved protocols and timelines. Execute chromatographic analyses including HPLC/LC, UPLC‑UV, and GC following validated methods. Conduct sample preparation (dilutions, extractions, filtrations, weighing, etc.) with strong attention to accuracy and traceability. Ensure all testing is performed in compliance with GMP, SOPs, and regulatory requirements. Assist in method development and optimization, including evaluating chromatographic conditions, sample prep techniques, and detection parameters. Record all activities in laboratory notebooks or electronic systems in accordance with ALCOA+ data integrity principles. Review and interpret analytical data, ensuring accuracy before reporting results. Operate, calibrate, and maintain analytical instruments (HPLC/UP...
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