Summary
Aaron Kehrer is a Director of Product Development with 12+ years of hands-on engineering and program leadership focused on bringing regulated medical devices from concept to market. He blends mechanical, electronic, microfluidic and software expertise—ranging from SolidWorks CAD and PCB design to firmware, web apps and automated fluid handling—to manage design, risk, verification/validation and quality systems. At in2being he not only leads client-facing requirements and regulatory strategy but also builds internal tools like in2ctrl and PathSurveyor to streamline document control and FDA classification work. His background includes designing injection-molded parts, optics positioning, and lab-on-a-chip cartridges, giving him a practical manufacturing-first perspective on DFM and process engineering. Known for translating complex regulatory requirements into executable development plans, he pairs technical depth with an entrepreneurial approach to tooling and process creation.
12 years of coding experience
8 years of employment as a software developer
Bachelor of Science in Engineering (B.S.E.), Bachelor of Science in Engineering (B.S.E.) at University of Michigan