The Clinical Software Developer will create and maintain software systems for medical devices, focusing on user interface development, troubleshooting, and testing in a team environment.

Responsible for global regulatory submissions for medical devices, including AI-enabled imaging technologies. Leads cross-functional compliance efforts and monitors regulatory changes.

The Product Quality Engineering Manager leads a team to ensure product quality for Computed Tomography systems, overseeing quality control, testing strategies, documentation, and compliance with medical regulations.