Experience working in a regulated industry (e.g., medical devices, aerospace, defense, finance), with direct experience contributing to design controls, risk management, and documentation for regulatory submissions (e.g., FDA 510(k),CE Marking). If you are passionate about hands-on hardware and firmware development, skilled in areas like mixed-signal design, FPGAs, test automation, and thrive in a fast-paced medical device startup, we encourage you to apply.