Craig Schlawin
About Craig Schlawin
Craig Schlawin is the Director of Quality at Boston Scientific, with extensive experience in quality assurance and engineering roles across various medical and biomedical companies.
Current Role at Boston Scientific
Craig Schlawin is currently serving as Director of Quality at Boston Scientific, a role he has held since 2014. Based in Minneapolis, Minnesota, United States, he brings a wealth of experience in quality assurance and engineering to the position. Boston Scientific is a global leader in medical devices, and Schlawin's role focuses on ensuring the highest standards of quality across the company's products and processes.
Past Roles at Boston Scientific
Before his current position, Craig Schlawin worked as an AQM Manager II at Boston Scientific from 2013 to 2014, for a duration of 10 months. In this capacity, he played a critical role in managing quality assurance processes, demonstrating his expertise and commitment to maintaining stringent quality standards.
Experience at Bridgepoint Medical, Inc.
Craig Schlawin has significant experience at Bridgepoint Medical, Inc., where he held two critical roles. From 2009 to 2013, he served as Vice President of Quality Assurance, overseeing quality assurance strategies for the company. Prior to this, from 2007 to 2009, he was the Quality Director, a role in which he managed and implemented quality control measures to enhance product reliability.
Professional History in Quality and Engineering
Craig Schlawin's extensive professional history includes roles such as Quality Assurance Manager at Lumen Biomedical (2006-2007), Sustaining Engineering Manager at Pulmonetic Systems (2003-2006), and Quality Manager at Acorn Cardiovascular (1998-2003). He has managed quality systems and engineering processes at multiple organizations, showcasing his comprehensive understanding of quality management across various medical technology companies.
Early Career in Engineering and Documentation
In his early career, Craig Schlawin worked at E-Med/IntraTherapeutics and Nellcor Puritan Bennett. At E-Med/IntraTherapeutics from 1997 to 2000, he held roles as Documentation Manager, Design Engineer, and Quality Engineer. Previously, at Nellcor Puritan Bennett from 1991 to 1997, he served as Design Services Manager and Senior Mechanical Engineer. These roles provided him with a strong foundation in engineering and quality documentation.