Jason March

Jason March is a seasoned Quality and Regulatory professional with nearly two decades of experience in the medical device and healthcare technology industries. Throughout his career, he has led quality and regulatory functions across a wide range of organizations, from large multinational manufacturers to emerging growth-stage companies, giving him a well-rounded perspective on what it takes to build and sustain effective quality systems at any scale.

Jason has deep expertise in Quality Management System design and governance, FDA and international regulatory compliance, post-market surveillance, complaint handling, and audit readiness. He has a consistent track record of stepping into complex compliance environments and driving meaningful, measurable improvements, whether that means achieving dramatic reductions in audit findings or building quality infrastructure from the ground up. He has supported regulatory submissions across the U.S., EU, and global markets, and has served as the primary quality liaison in regulatory inspections throughout his career. Beyond the technical side, Jason is known for partnering closely with executive, engineering, and clinical teams to align quality strategy with business objectives.

As Vice President of Quality and Regulatory at bioDesign Group Technologies, Jason brings that same depth of experience to a company on the leading edge of patient-centered medical device innovation. bioDesign is focused on developing universally designed products aimed at expanding access to real-world healthcare, with an active FDA 510(k) pathway and a global regulatory roadmap on the horizon. Jason's role is focused on building the regulatory and quality infrastructure needed to bring these products to market with the rigor and readiness that patients and regulators expect.