Setu Gupta Email & Phone Number

Etobicoke, Ontario, Canada

•Initiate, plan, organize, conduct, and troubleshoot technical work in radiochemical and isotope separations, chemical and radiochemical synthesis.•Conduct all work in accordance with Kinectrics’ safety policies.•Develop new methods, perform hands-on experiments, draft written procedures, experimental plans, and reports.•Prepare project updates as required and participate in project update meetings when requested.•Keep informed on the latest technical developments and techniques… Show more •Initiate, plan, organize, conduct, and troubleshoot technical work in radiochemical and isotope separations, chemical and radiochemical synthesis.•Conduct all work in accordance with Kinectrics’ safety policies.•Develop new methods, perform hands-on experiments, draft written procedures, experimental plans, and reports.•Prepare project updates as required and participate in project update meetings when requested.•Keep informed on the latest technical developments and techniques in radiochemical synthesis and analysis.•Proven familiarity with process and analytical instrumentation, including analytical and preparative scale LC, radio-chromatographic techniques, ICP-MS, gamma-spectroscopy, and other traditional chemical and physical techniques.•Understanding of ALARA and other safe lab techniques.•Demonstrated ability to work within cross-functional teams. Show less

Hamilton, Ontario

•Evaluate and Lead Deviations, Out of Specifications (OOS), Corrective Action / Preventive Action (CAPA) and Non- Conformance (NC) •Develop and validate analytical test methods following cGMP guidelines of different regulatory agencies (FDA, Health Canada and Ph. Eur.)•Experience in initiating, auditing, managing, and executing projects; work with team and manager to ensure high level of data quality in a fast paced environment•Conduct investigations for out of… Show more •Evaluate and Lead Deviations, Out of Specifications (OOS), Corrective Action / Preventive Action (CAPA) and Non- Conformance (NC) •Develop and validate analytical test methods following cGMP guidelines of different regulatory agencies (FDA, Health Canada and Ph. Eur.)•Experience in initiating, auditing, managing, and executing projects; work with team and manager to ensure high level of data quality in a fast paced environment•Conduct investigations for out of specification and non-conformance; provide change control and, corrective action and preventive action as required•Author, revise, and review technical documents, including SOPs, validation documents, standard test methods according to good documentation practices and report•Perform analysis of raw material, in-process, finished products and drug formulation using analytical instruments like HPLC ( PDA and UV detector ), GC (MS and FID detector), pH meter, TLC scanner, pipette and analytical balance•Perform the cleaning, calibration, preventative maintenance and qualification of laboratory instruments; assist with inventory and management of Quality Control materials•Conduct peer review of laboratory records as well as responsible for routine monthly environmental monitoring according to standard operating procedures including microbiological tests•Compiles all data obtained from testing and observations; completes report summaries as per established SOPs•Provides technical troubleshooting support or training to other team members where appropriate•Familiar with software applications like LIMS (Laboratory Information Management System), Chromeleon, Empower, Chemstation and other relevant instrument handling application software•Proficiency in MS Office (Excel, PowerPoint, Word, Outlook)•Strong Written and Oral communication and presentation skills Show less

Burlington, Ontario

•Responsible for analyzing environmental samples of air/solid/water using Agilent GC/MS and Perkin Elmer turbo-matrix systems•Interpret data using Agilent Chemstation, conduct calculations, and transfer data through LIMS to finalize report•Currently using established methods/schedules and standard operating procedure to produce quality data with QA/QC requirements•Operate and maintain laboratory equipment and apparatus•Evaluate data and troubleshoot problems with the… Show more •Responsible for analyzing environmental samples of air/solid/water using Agilent GC/MS and Perkin Elmer turbo-matrix systems•Interpret data using Agilent Chemstation, conduct calculations, and transfer data through LIMS to finalize report•Currently using established methods/schedules and standard operating procedure to produce quality data with QA/QC requirements•Operate and maintain laboratory equipment and apparatus•Evaluate data and troubleshoot problems with the data/extraction/ instrumentation•Prepare standard solutions of gas or liquid and reagents•Perform chromatography, separation technique, instrument calibration, trouble shooting and maintenance•Meet company standards pertaining to quantity and quality of work performed on an ongoing basis •Assists in the training of new staff members on instrumentation software and operation•Assists in development of standards, procedures and health and safety hazards•Compile records of analytical results•Involve in method development process for new and upcoming projects•Work with supervisor and laboratory manager to ensure high level of data quality•Organize workload to meet Turn Around Times (TATs)•Knowledge of compendia, ICH, GMP and GLP Show less

Ontario, Canada

I was involved in multi-step synthesis of organic compounds which included chemical separation and characterization through different spectroscopic techniques.

Ontario, Canada

I instructed undergraduate students in organic chemistry laboratory techniques. In addition, I proctor and assess examinations for undergraduate chemistry courses

Masters, Chemistry

B.Pharm, Pharmacy