Curtis Jensen

Curtis Jensen is currently the VP Quality and Regulatory Affairs at Titan Medical. Prior to this, they were the Sr. Regulatory Affairs at EKOS Corporation from December 2015 to March 2017 where they were responsible for worldwide regulatory approval for a new ultrasound pulmonary embolism catheter. Curtis has also been the Quality Manager at Ceramatec, Inc from April 2008 to August 2010, the CAPA Manager at GE Healthcare from January 2007 to December 2008, and the Quality Manager at Bausch & Lomb from January 2000 to December 2002. In addition, they have also been the Vice President of Quality and Regulatory Affairs at Domain Surgical, Inc from August 2010 to November 2015, the Principal Manager at Amphora LLC from January 2009 to November 2015, and the Quality and Regulatory Director at Iomed, Inc from January 2002 to December 2007. Curtis began their career in quality assurance as the Field Assurance Manager at C.R. Bard from January 1992 to December 2000.

Curtis Jensen has a BS in Electrical Engineering from Utah State University and an MS in Applied Mathematics from The Johns Hopkins University.

Some of their coworkers include Sachin A. Sankholkar - VP Marketing, Chris Seibert - VP Business Development, and Jasminder Brar - Director of Strategic Development and Intellectual Property. Curtis Jensen reports to David J. McNally, President & CEO.