Laura LeBoeuf, Vice President of Quality and Regulatory Affairs

Laura LeBoeuf joined SpineSmith as Quality Assurance Specialist in 2009 with over 20 years of experience in the medical device industry. She is currently the Vice President of Quality & Regulatory Affairs with responsibility for all aspects of the company’s quality system and regulatory compliance efforts.

Laura’s career in medical devices began in 1986 as a Quality Engineer supporting manufacturing and product development efforts related to heart valve replacement and repair. Her medical device experience includes quality, reliability, manufacturing, and product engineering as well as project management. Her work in medical device engineering and engineering management encompasses products for cardiac, orthopedic, general surgery, diagnostic and spine applications.

Laura holds a Bachelor of Science degree in Industrial Engineering from Texas A& M University.