Principal Software Engineer – Azurion Eye – Plymouth, MN

Philips•Plymouth, MN

7d•$146,475 - $234,360•Onsite

About The Position

The Principal Software Engineer will lead the development, analysis, validation, and documentation of data-driven and machine-learning-enabled workflows for clinical imaging software within the Azurion Eye program, collaborating with AI/ML engineers, software engineers, product owners, testers, and cross-functional stakeholders to improve clinical workflows and efficiency.

Requirements

Bachelor’s or Master’s degree in Computer Science, Computer Engineering, Software Engineering or related field.
12+ years of software development experience, including 10+ years of C++ development experience with C++ used in their current or most recent role.
Experience integrating AI capabilities into software platforms and optimizing intelligent workflows, with knowledge of DICOM, HL7, FHIR, PACS, RIS, or HIS.
Experience with modern development and DevOps tools such as Visual Studio, Azure DevOps, Git, CMake, Jenkins, and GitHub Actions.
Experience working in Agile/Scrum or Kanban environments and developing software within regulated medical-device environments; knowledge of IEC 62304, IEC 82304, ISO 13485, and ISO 14971.
Must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

Responsibilities

Collaborate with Product Owners, Software Architects, Systems Engineers, and Testers to translate requirements into medical imaging and system integration features.
Leverage strong C++ expertise to develop clinical and messaging features that enable integration between IntraSight and Azurion systems.
Break down requirements into BDD scenarios and contribute to Agile planning and predictable delivery of roadmap features.
Apply strong software architecture, design, coding, and integration practices while ensuring solutions align with the broader software platform architecture.
Lead software documentation and participate in risk management activities, including FMEA, while adhering to Philips Agile QMS and medical-device regulatory requirements.