medical-device-software jobs in San Diego

Senior Staff Software Engineer leading technical strategy and architecture for embedded, connected medical-device software. Will resolve cross-functional technical issues spanning software, hardware, systems, and quality; identify architectural improvements and technical debt; mentor engineers; and drive design reviews and coding standards.…See more Requires 12+ years of professional software development with medical-device or regulated systems experience, proficiency in C/C++, embedded Linux/RTOS, and network-connected device design.

Lead and scale a software organization at a medical-device company from lean team to commercial scale, reporting to VP of R&D. Responsibilities include hiring and mentoring engineers, establishing coding standards and workflows, translating executive vision into technical strategy and roadmaps, staying hands-on with prototyping and code review, and coordinating across hardware, data science, regulatory, and executive functions.…See more Requires 10–15+ years in software development with 5+ years managing technical teams, experience shipping mobile apps and cloud backends for connected devices, regulated-industry background (medical device preferred), and fluency in modern DevOps, CI/CD, and automation testing.

Senior Staff Software Engineer leading technical strategy and problem-solving across software, systems, electrical, and quality functions for regulated medical-device products. Responsible for architecting embedded, connected, network-enabled systems; resolving cross-functional technical challenges; mentoring engineers; and ensuring compliance with FDA, IVDR, and international regulatory standards.…See more Requires 12+ years of professional software development experience with embedded or software-intensive products, deep proficiency in C/C++, embedded Linux or RTOS, and proven expertise in networked device design, secure communications, and design-control processes for medical devices or safety-critical systems.

Software Engineer II will design and develop embedded software for Genalyte's Merlin photonic diagnostic platform, a medical device requiring adherence to FDA/medical device software standards. The role involves developing embedded software components, creating software tools for testing and integration, executing test protocols, and troubleshooting system functionality.…See more The engineer will work with device-to-cloud interfaces, low-level hardware controllers (motors, robots, sensors), and collaborate cross-functionally while mentoring junior engineers. Required skills include C/C++/C#/Python (.NET preferred), embedded systems design, build systems, unit testing, networking, Unix/Windows, and Jira/Confluence.

Senior iOS Software Engineer responsible for designing, developing, and delivering high-quality Swift-based iOS applications and SDKs for medical device products. Requires 5+ years of software development experience and 3+ years of iOS-specific development.…See more Responsibilities include implementing unit and UI tests, mentoring developers, ensuring software quality and architectural consistency, and collaborating with cross-functional teams (product, UX, QA, scrum) in an Agile environment. Must follow design assurance SOPs and support compliance with FDA and HIPAA regulations.

Senior/Staff Software Engineer role developing driver, diagnostic, and embedded software for intravascular ultrasound systems using C++. Responsibilities include architecting and designing embedded software, creating detailed design documentation (specifications, architecture, design documents), developing driver software for hardware-application communication, and interfacing with cross-functional teams including hardware, electrical, and system engineers.…See more Requires 8+ years of embedded/software development experience, strong C++ expertise, BS/MS in Computer Science or related field, and experience creating detailed design documentation; digital signal/image processing and CUDA knowledge are preferred.

Lead software development for an FDA-cleared blood testing platform, overseeing instrument software, application software, cloud connectivity, cybersecurity, and software quality systems. Manage the full software development lifecycle including requirements, risk management, design controls, verification and validation, and regulatory compliance.…See more Work closely with Quality and Regulatory Affairs on FDA submissions, audits, documentation, and post-market support. Direct strategy, roadmap planning, architecture, and release management for a regulated in vitro diagnostic (IVD) medical device.