Senior Software Engineer
- Edinburgh
- Permanent
- Full-time
- 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.
- 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 WinForms, or Win32, 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) and ISO 14971 and developing to and compliance with IEC62304 is a big plus.
- Experience in development of integrated (hardware and software) medical devices is a plus
- Experience with Containers, DevOps environments is a plus.
- Working knowledge of software development tools such as Azure DevOps, Git, etc. is a plus.
- Strong understanding of Continuous Delivery and Agile development is a plus.
- Experience working effectively with international teams in Europe, India and the US.