Samd Jobs

NeuroLogica seeks a Senior Regulatory Affairs Specialist to lead global regulatory submissions and compliance for CT, X‑ray, ultrasound and AI-enabled imaging products.

Experienced healthcare and technology attorney wanted to lead legal strategy for ResMed’s Residential Care Software business, advising on SaaS commercial deals, AI/product risk, privacy, and global compliance.

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.

Experienced document control professional needed to own DMS maintenance, ensure regulatory-compliant records, and support audits for a remote, regulated-healthcare-focused company.

Be the frontline technical responder for Viz.ai customers, troubleshooting SaaS, cloud, and on-prem issues while collaborating with internal teams to deliver excellent customer outcomes.

ResMed seeks a Senior Manager of Design Quality (Digital Product) to lead a product quality team and act as the primary QA representative for software and SaMD projects, ensuring design control, risk management and regulatory compliance.

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

GE HealthCare's Diagnostic Cardiology unit is hiring a Program Director to lead PMO activities and deliver multi-generational ECG product roadmaps from concept through commercial launch.

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.

Lead cross-functional software and ML engineering at a venture-backed medical AI company developing wearable biosensors and FDA-regulated SaMD.

Serve as Associate General Counsel, Senior Director of Regulatory Compliance & Privacy to lead Oura’s global regulatory, privacy, and corporate compliance programs for wearable and digital health products.

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.

Lead the global strategy and execution for Lunit CXR, driving product vision, clinical validation, and market adoption of an AI-powered chest x‑ray diagnostic solution.

Lead technical project delivery and regulatory-compliant documentation for Oura's SaMD products, coordinating cross-functional teams to meet safety, quality, and regulatory requirements.