7 years of cross-functional experience in analytical research and QC. Projects lead capabilities. Expertise in analytical method development and Validation. Well-versed with and expertise in Chromatography and Spectroscopy techniques like HPLC, UPLC, GC, TLC, HPTLC, LCMS, FTIR, UV spectroscopy. Having Knowledge of Dissolution method development and IVRT method development. Handled various drug products as Solid, Liquid, Semi-Solid, Soft-Gel Capsules. Experienced in Routine, Stability, and Validation Data review, Test Method Drafting, Analytical Method Development Report Preparations, Method Validation Protocol, and Report Preparation. Good Knowledge of USFDA audits and their preparations. Well Versed with cGMP, GLP, GDP. DMF data review. Having Problem-solving capabilities and deliver work within the stipulated time. A team player and find the best fit according to expertise and multi-task professional.
Research Associate II Analytical R
Mobile, 50% within India.
Mobile, Ready to relocate in UAE, USA, UK. With Valid Work Visa and Relocation Assistance.
Working Hours, 8 Hrs and More if required