Iec 62304 Jobs

Experienced Validation Engineer III needed to lead complex design verification and validation efforts for medical device software systems, ensuring regulatory compliance and driving process innovation.

Foresight Diagnostics seeks a Senior Specialist, Regulatory Affairs to lead US regulatory strategy and submissions for next-generation sequencing-based IVD products while partnering cross-functionally through development and lifecycle management.

DeepHealth seeks a hands-on QA/RA Project Manager to drive quality, regulatory readiness, and cross-functional delivery for medical device software and digital health products in a fully remote role.

Lead verification for cloud-connected medical devices and mobile health applications as a Senior Verification Engineer/Lead based in Pleasanton, CA with IBA InfoTech.

Lead systems engineering for Philips’ next-generation interventional platform in San Diego, guiding cross-functional teams and external partners from requirements through launch while ensuring regulatory compliance.

Experienced firmware engineer needed to develop and optimize embedded C/C++ firmware for ARM Cortex-M medical imaging platforms with emphasis on real-time performance and regulatory compliance.

Lead product software strategy and regulatory-compliant development for a fast-growing molecular diagnostics company, driving validated, secure solutions that impact patient outcomes.

Artera is hiring a Systems Engineer to lead requirements, risk management, system architecture, and usability engineering for its AI medical-device products.

Foresight Diagnostics seeks an experienced VP of Product Software to lead regulated medical device software strategy, compliance, and validated product delivery across cross-functional teams.

Abbott's Lingo division is hiring a Quality Engineer II to lead design control, CAPA, and risk-management activities for medical devices and SaMD from our Alameda, CA site.

Alphatec Spine seeks an experienced software engineering director to lead cross-functional teams developing embedded, mobile, web, and cloud solutions for intra-operative medical devices.

Lead systems-level solutions and sustaining engineering at Insulet as a Principal Systems Engineer, providing technical leadership across design, post-market support, and regulatory-compliant lifecycle activities.

Lead cross-functional continuous improvement for design quality at Insulet, implementing SDLC best practices and regulatory-aligned process improvements to accelerate compliant product development.

Abbott seeks a Senior Design Control Software Quality Engineer to validate and maintain Lingo product software and computerized quality systems in compliance with medical device regulations.

Lead requirements engineering and traceability for Insulet's next-gen wearable medical device software, ensuring compliance and clear, testable requirements across mobile and cloud systems.

Experienced systems engineering leader needed to drive sustaining engineering, root-cause resolution, and regulatory-compliant product improvements for Insulet's wearable drug-delivery platform in a hybrid Massachusetts role.

Abbott is hiring a Software Quality Engineer II in Sylmar, CA to lead software validation, quality engineering, and regulatory compliance for non-product medical device software.

Lead the design and delivery of safety‑critical embedded firmware (C/C++) for Osteal Therapeutics' next‑generation drug‑delivery devices as a Senior or Principal Embedded Software Engineer based in Dallas, TX.

Alcon is hiring a Principal Software Systems Engineer in Lake Forest, CA to own system and software requirements, ensure regulatory compliance, and architect safe, reliable medical digital platform solutions.

Oura is hiring a Senior Program Manager to drive SaMD program execution and regulatory compliance across cross-functional teams to deliver high-quality medical device software.