Responsible for Q-TOF LCMS based method development and qualification for intact massanalysis, Peptide mapping, identification, quantification and characterization of recombinantProteins, Small molecules, & monoclonal Antibodies (Biosimilars) using Q-TOF LCMS Mass hunter software.Responsible for method development and optimization of in-Gel digestion of recombinantproteins for Q-TOF LCMS analysis and performing sequence coverage using Mass huntersoftware.Responsible for… Show more Responsible for Q-TOF LCMS based method development and qualification for intact massanalysis, Peptide mapping, identification, quantification and characterization of recombinantProteins, Small molecules, & monoclonal Antibodies (Biosimilars) using Q-TOF LCMS Mass hunter software.Responsible for method development and optimization of in-Gel digestion of recombinantproteins for Q-TOF LCMS analysis and performing sequence coverage using Mass huntersoftware.Responsible for calibration of Q-TOF LCMS, HPLC.Responsible for preparing of Standard Operating Protocol (SOP), Raw data Sheets (RDS),User Requirement Specification (URS), Master qualification protocol (MQP), Method ofAnalysis (MOA) and Developmental Report (DR).Responsible for coordinating with vendors and preparing/documenting the change controlfor inclusion of new SOPs, inclusion of Instrument/Equipment IQ,OQ,PQ and all deviationsas per approved Bioanalytical laboratory SOPs and GLP requirement.Involved in establishment of new Analytical and Characterization lab comprising high endanalytical equipments like Q-TOF LCMS (Thermo scientific orbitrap exploris 240 & Agilent 6545XT bio Q-TOF). Show less

Responsible for performing routine analysis of assigned projects using analytical techniquesand instrumentation, such as HPLC (RP,SEC), LCMS, SDS PAGE for samples of differentpharmaceutical dosage forms / phases / stages (Biosimilars).Responsible for data analysis, processing, compilation, documenting the activity andpresenting it to Team lead pertaining to the study when required.Responsible for maintaining and ordering of inventories for chemicals… Show more Responsible for performing routine analysis of assigned projects using analytical techniquesand instrumentation, such as HPLC (RP,SEC), LCMS, SDS PAGE for samples of differentpharmaceutical dosage forms / phases / stages (Biosimilars).Responsible for data analysis, processing, compilation, documenting the activity andpresenting it to Team lead pertaining to the study when required.Responsible for maintaining and ordering of inventories for chemicals, accessories,consumables & stationary.Maintenance of accurate and timely records of Lab Note Books, Usage books, Calibrationplanner, Annual maintenance contracts & Preventive maintenance contracts as per SOP & GLP. Show less