Jon Stevens

As the Vice President of Quality and Regulatory, Jon is responsible for all aspects of product quality assurance, compliance, technical communications, clinical claims, and regulatory affairs at all Verathon sites globally. The Q&R team partners with the business to develop, manufacture, and distribute products and solutions that meet the high standards of our patients, customers, and regulators. Jon is passionate about creating a culture of quality that will give Verathon a sustained competitive advantage by developing systems which are both compliant and pragmatic.         

Jon comes from multiple fast paced and pioneering medical device companies. He previously worked at Philips as global Head of Quality for the Hospital Patient Monitoring business. Jon also held various leadership roles at Medtronic in California, and Fisher & Paykel Healthcare in New Zealand. He has led companies through difficult quality and regulatory landscapes, including Consent Decrees, FDA Warning Letters, and remediation for the new EU Medical Device Regulation. He has a Master's in Business Administration from University of Auckland, New Zealand, and a Bachelors in Biomedical Engineering from University of California, Irvine.