Senior Software Engineer

Overview

At Spacelabs Healthcare, we are on a mission to provide continuous innovation in healthcare technology for better clinical and economic outcomes. Our scalable solutions deliver critical patient data across local and remote systems, enable better-informed decisions, increase efficiencies, and create a safer environment for patients.

The Senior Software Engineer will be a member of the Spacelabs R&D engineering team working on the development of Spacelabs Patient Monitoring and Connectivity (PMC) products. This position requires a deep understanding of solid design and development practices and the ability to apply those to Spacelabs product development. The person will be responsible for developing and delivering software that supports the next generation patient monitoring products.

They will work with other cross-functional members to provide technical software level expertise, and solutions to engineering problems.

A key element of this role includes advocating for and designing products that meet the functional, performance and cybersecurity needs of our customers. A strong systems approach to product development will be necessary in this role. You will spend your time as a hands‑on engineer and a technical leader. Our team plays a key role in building software products and features.

You will use a wide range of technologies, programming languages and systems. You will be involved in architecture/design of new features and functionality, as well as the development and implementation.

• Work with the software team and other cross-functional project staff to define requirements related to patient monitors.
• Participate in cross‑functional reviews of software requirements, architecture, software design, connectivity interface design and user interface design.
• Participate in the component design efforts. Understand and design to existing interface specifications.
• Participate in the definition of architectures, software designs, and product workflows.
• Design, write, debug, document and release software used for communication, storage and analysis of patient physiological information in an agile development environment.
• Ensure on‑time delivery of software including design documentation, unit tests and other required artifacts.
• Hold yourself and other engineers to high standards while maintaining friendly, respectful relationships.
• Uphold the Company’s core values of Integrity, Innovation, Accountability, and Teamwork.
• Demonstrate behavior consistent with the Company’s Code of Ethics and Conduct. Ensure that team members (direct or indirect reports) are trained and evaluated on their knowledge and adherence to the Company’s values, Code of Ethics and Conduct, and applicable compliance policies.
• Duties may be modified or assigned at any time to meet the needs of the business.
• Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork.
• Demonstrate behavior consistent with the company’s Code of Ethics and Conduct.
• It is the responsibility of every employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem.
• Duties may be modified or assigned at any time to meet the needs of the business.

• Bachelor of Science degree in Computer Engineering or Computer Science, Mathematics or a related Engineering discipline
• 8+ years of relevant software experience required.
• 4+ years of programming in C++ 11 or higher utilizing Object-Oriented Programming (OOP) concepts and techniques is required
• Experience in utilizing multi-threading techniques is required.
• Demonstrated experience with desktop Linux application development in an embedded environment is required.
• Experience with Qt/QML is a big plus.
• Experince with desktop UI development in at least 1 UI framework such as WPF, WinUI 3, UWP, etc. (not Win Forms, or Win
  32, or web-based) is a plus.
• Experience working in a regulated development environment (finance, medical, defense, aerospace, etc.) is a plus.
• Experience in product development of medical devices under Design Control (21 CFR Part 820)…