• Principle team member in the development, characterization and verification of new chemiluminescent substrate for a next generation high-throughput immunoassay platform• Investigating clinical and customer sample discrepancies, reporting out to high levels of the organization• Designing and implementing new hardware solutions to for a new high-throughput immunoassay platform to improve throughput and substrate stability• Provide guidance to new product development teams to optimize new substrate-assay interactions, including SARS-CoV-2 • Assist leadership teams in scoping future breakthrough technologies to maintain competitive edge in the market• Lead large cross functional team of QC, RA and process developers to complete complex test method validations• Write new critical raw material test SOPs as a part of transfer from development to manufacturing • Generate scripts to increase the speed of complex data reduction and analysis

• Developed and executed protocols for the early design feasibility and characterization of a next generation high-throughput immunoassay platform• Wrote and refined assay protocol files for automated immunoassay systems• Presented concise data and conclusions to leadership teams representing various teams and levels of the organization• Utilized various Danaher tools and principles, including Daily Management, PSP, 5S and Kamishibai

• Responsible for lab and equipment maintenance

• Tested and analyzed data from development lots of biological indicators in hydrogen peroxide sterilizers• Performed titrations of chemical disinfectants

• Assisted in development and commercialization of new immunoassays for the Access2 and DxI600/800 Immunoassay systems• Performed multiple studies of assay reagent pack lot to lot variability, including assay linearity and aging pack stability• Studied paramagnetic particles builds of assays in redevelopment• Investigated thermal stability of 4 commercially released assays in prototype instruments being developed in compliance with Reduction of Hazardous Substances Guidelines• Prepared and screened large volumes of patient serum and plasma samples to be used in verification testing• Work closely with multiple project teams in an ISO9000 and FDA regulated environment• Keep organized laboratory records following GLP and GMP guidelines• Follow the practices of lean manufacturing and the 5S system• Participate in review sessions of verification and validation testing data • Present findings to associates from other departments

•Responsible for growth of recombinant bacterial cultures•Performed purification of proteins and analyzed using western blots and gel electrophoresis•Assited in development of protein binding assays•Worked closely with university faculty and graduate students in a research laboratory•Kept organized laboratory records with experimental data•Participated in lab meetings with a team of scientists to finish projects in a timely manner•Conducted upkeep and maintenance of laboratory equipment•Prepared chemical reagents•Cleaned and sterilized cell culture and general laboratory materials

•Worked with and led others in producing large quantities of high quality windshields, roofs, doors and similar products.•Performed general assembly and drape forming.•Identified quality problems communicated with coworkers to discover the source and how to remedy them

•Provided customer service to a large number of customers on a daily basis in house and in their homes.•Communicated with kitchen staff and customers, both over the phone and in person, regarding orders to ensure meals were delivered in a timely manner.•Maintained clean and stocked work stations to assist the other kitchen workers.