Working full-time with a designation in 'The QUALITY CONTROL department as an Analyst in the In-Prosses and Finished product section. Well-versed with pharma analytical instruments like UV, IR spectroscopy, water content, RF spectroscopy, Thin layer chromatography, disintegration, dissolution, hardness, and friability apparatus. Primary duties include an in-depth understanding of USFDA, TGA, GLP, SOPs, and/or other applicable guidelines and ensuring QC testing is performed in accordance with these guidelines

Gained knowledge about the process of BMR, GMP, GLP, Quality Control, SOPs, HPLC, HPTLC,UV Spectroscopy, Photometry, Spectrophotometer, pH meter, calibration, Dissolution, Sonicator,Disintegration test, granulation, compression, coating, Blister Packing in the Formulation of solid,liquid, semisolid dosage form