Director Of Product Quality
Current-Lead Human Factors Evaluations for Medical Device, in compliance with IEC 62366 and FDA Guidance: Applying human Factors and Usability Engineering to Medical Devices, February 3, 2016, in support of FDA submission-Manage supplier evaluations-Assess risks to design, use/misuse, cybersecurity, and off-the-shelf software of a medical device-Perform formative.