GE Healthcare

This role focuses on ensuring AI-based clinical features for ultrasound systems comply with global regulatory requirements, particularly FDA regulations for AI-enabled medical devices. The AI Regulatory Engineer will define and execute AI regulatory strategies, risk management, and submission pathways across the full product lifecycle, working closely with AI engineering, clinical, quality, and product management teams.

Hardware engineer with expertise in system electrical design, power design, EMC/EMI, electrical safety, high power distribution units, and board design for GE Healthcare.

Responsible for planning and implementing verification methodologies for PET medical products, ensuring system and sub-system requirements are met. This involves reviewing designs, verifying functionality, determining testing environments, analyzing failures, and collaborating with development teams. The role requires a strong background in multi-disciplinary medical product testing and software QA processes.

Senior System Engineer role at GE Medical Systems Israel Ltd, focusing on the design, development, integration, and verification of complex medical imaging systems. Responsibilities include translating clinical needs into technical requirements, ensuring performance, safety, and regulatory compliance, and collaborating with cross-functional teams. Requires 5+ years of experience in system engineering within the medical device industry, strong understanding of medical device regulations, and risk management experience.