As a systems engineer working on software as a medical device, you'll be at the intersection of innovation and regulation, collaborating with regulatory, clinical, marketing, and engineering teams to push the boundaries of what's possible in healthcare technology. You'll see the big picture across regulated projects, connecting dots between teams and disciplines while thriving in ambiguous, fast-moving environments.Your Key Responsibilities-Support design and architecture of health regulatory and sensor software applications-Collaborate with cross-functional partners to translate bold product visions into actionable user requirements and engineering designs-Translate complex technical and regulatory concepts for diverse audiences, from engineers to executives-Lead strategic initiatives that increase product development efficiency and scalability, and process optimization-Develop, manage, and maintain design history files and regulatory deliverables-Conduct impact analysis on design changes and facilitate trade-off discussions across stakeholder groupsWhat We're Looking ForWhy This Role Matters