• Create and own Use/Misuse Failure Mode Effect Analysis risk document for Inhaled Anesthetic product. • Write formative study protocols, conduct formative studies, evaluate and report data for Inhaled Anesthetic product and Peritoneal dialysis devices• Attend multiple renal ride alongs to meet, recruit and interact with dialysis patients • Organize and facilitate sessions for a sound panel with patients, analyze data and report patient feedback to design team

• Understand design process and work on verification testing of medical device while under strict timelines• Write test objectives, execute test scripts on medical devices and evaluate tests to verify/validate a system is working as intended• Collaborate with Systems team and other cross-functional groups to find root cause of problems with device• Experience with working in a biohazard laboratory • Underwent 2 day risk management class and familiar with ISO standards and good documentation practices

-Contributed in aspects of designing and commercializing a global consumer good-Organized, coded, tested and lead a manufacturing trial creating goods for research studies-Organized and led consumer study of test products created in trial-Participated in a multi-functional, multi-national team to evaluate study results and improve product for target consumers-Created study protocols and data reports based on global studies

-Tested various types of software and validated applications working on ViewPoint -Assisted test engineers in other software platforms, FactoryTalk Studio

-Assisted Product Managers in releasing new products for Industrial Computer Business and PanelView Plus 6-Developed cultural competencies, experience working with international employees, talking to customers-Organized, collaborated and setup booths with partner companies at Automation Fair Showcase-Analyzed market competitors and created documentation and reports for product managers and directors