• Having 12+ years’ of exposure in Quality (QC & QA) department of Pharmaceutical industry. In depth understanding of cGMP, GLP, documentation system, Quality management system and USFDA, MHRA, ISO, WHO and other regulations.
• Well versed in generation, maintenance and revision of SOPs, specifications, procedures, training, OOS/Incident/change investigations and other documentation systems.
• Well versed in all modern instrumentation such as HPLC, GC, UV, IR, etc., as well as various other analytical techniques.
• Having exposure of various analytical technique, Analytical Method transfer activity, Method Validation, Instrument Qualification and Calibration, Documentation work related Q....