Position is for a senior-level individual contributor responsible for leading and executing software-level activities for complex, regulated medical devices. This role focuses on capturing and translating customer and stakeholder requirements into clear, actionable requirements and specifications, ensuring alignment across development and testing teams. Acting as a subject matter expert, this role provides technical leadership and guidance to deliver high-quality software solutions that meet regulatory standards and customer needs. Based in Pleasanton, CA, the role requires strong technical depth, systems thinking, and the ability to operate with minimal supervision. The engineer collaborates closely with cross-functional teams—including Systems, Software, Quality, Clinical, and Regulatory—and coordinates with global engineering personnel to ensure alignment, resolve interdependencies, and drive successful project completion.
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Job Type
Full-time
Career Level
Senior