Chris Miller is Executive Director of Regulatory Affairs and Quality at LSI SOLUTIONS®. Chris’ 31 year career includes an extensive background in engineering, design, intellectual property, and regulatory affairs, spanning a wide variety of electromechanical, imaging, bioinformatics, semiconductor, MEMS, and medical device technologies, the last 11 years in the cardiac and general surgical medical device space at LSI SOLUTIONS®.  

‍

Chris leads and provides strategic direction to a dynamic, talented group of 95+ professionals comprising LSI’s U.S., European, International, Surgical Science, Post-market & Lifecycle Compliance, Quality Assurance, Quality Control, and IP Teams. Chris has the proven ability to ethically and effectively navigate complex and nuanced issues, while setting high standards for his teams. Chris builds talented, flexible teams, creating an environment where challenges are positively embraced and knowledge is creatively and productively applied in furtherance of LSI’s corporate mission and goals.  

‍

Since Chris took on the Director role in 2018, his teams have enabled impressive growth in the number of countries where LSI products are cleared from 46 to 69 countries (43% increase), including expansion from 31 to 99 cleared product SKUs (219% increase), for a combined increase from 226 to 1581 unique SKU-Country combinations (600% increase) cleared and managed within LSI’s Quality Management System, while maintaining compliance with ever-changing worldwide regulations.  

‍

Chris held technical and intellectual property roles at Fortune 500 companies and law firms before joining LSI SOLUTIONS® in 2013. He earned a Bachelor’s degree in Electrical Engineering with Honors from Syracuse University, and he is also licensed to practice patent law.