Simon Haque

Background

About Simon Haque

Having 2+ years of working experience in Formulation Analytical R&D, Oral Solid Dosage. Have excellent exposure towards analytical instruments like Dissolution Apparatus type I & II, KF auto titrator, HPLC, UPLC and techniques like Analytical method development and validation, Assay, Related substances, Content Uniformity, Blend uniformity and Dissolution Science considering subsequent market and requirement. Some of my key day-to-day activities involve, • Performing in-process, Stability study analysis, Dissolution, Water Content, Assay, and RS of the drug product to optimize development and to know the behaviour of the drug product at storage conditions. • Day-to-day planning, Inventory management and handling of team activities for completion and delivery of tasks in timelines. • Project-related discussions and meetings with cross-functional teams. • Supporting QC by solving analytical issues raised during analysis. • Performing calibration of analytical instruments. • Online documentation & ensure overall compliance with the organizational guidelines. My goal is to keep excelling and learning throughout.