Mark Schnapf

Mark Schnapf is a seasoned professional in the medical device industry with extensive experience in quality assurance, regulatory compliance, and materials analysis. Currently serving as a Materials Analyst (PFAS) at RQM+, Mark focuses on the assessment of polymer materials in cardiovascular devices. Previously, Mark held key positions at Boston Scientific and Medtronic, where responsibilities included integration of quality systems, compliance with EU MDR for cardiovascular products, and oversight of sterile manufacturing processes. Career highlights also include roles in regulatory documentation, quality supervision, and contributions to FDA submissions. Mark holds a Bachelor's Degree in Medical Technology from the University of Minnesota - Twin Cities.