QA/QC Director
Michael Healy has more than 30 years of medical device experience encompassing development, manufacturing, distribution and quality. Throughout his career he has implemented several FDA and ISO compliant quality systems for manufacturers of Class I, II and III medical devices.
Prior to joining Tryton, Michael held positions at Marquette Medical, GE Medical, Hill-Rom, Cook Endoscopy, Teleflex and provided Quality System consulting to Boston Scientific Corporation. During his time with these medical device companies Michael held responsibility for all aspects of the quality system and functioned as the Management Representative. Michael has been instrumental at resolving FDA and ISO issues at these companies.
Michael earned his B.S. degree in electrical engineering. Additionally he holds Six Sigma certification from GE Medical along with Manager of Quality/Organizational Excellence certification, Quality Auditor certification and Biomedical Auditor certification from American Society for Quality (ASQ).