Software Engineer III
Spacelabs
- Snoqualmie, WA
- Permanent
- Full-time
- Perform all work in compliance with applicable regulations and Spacelabs design controls.
- Work with the team and other cross-functional staff to define requirements related to patient bedside monitors.
- Participate in systems level requirements definition, architecture, design, and external communications/connectivity interface designs.
- Participate in component design efforts. Understand and design according to existing interface specifications.
- Design, write, debug, document, and release software used for communication, storage, and analysis of patient physiological information.
- Work with global teams consisting of Spacelabs employees and contract resources.
- Ensure on-time delivery of software, including design documentation and unit tests necessary to maintain the software.
- Use your experience to make smart engineering decisions and own critical areas of a product used by millions of customers.
- Participate in the design, implementation, and delivery of large engineering projects that interact with multiple teams.
- Mentor other junior engineers to help them grow both technically and professionally.
- Work with the Software Architects to define designs and workflows that enable working through other engineers.
- Ensure consistency of the team you are on and those teams you integrate with.
- Ideate and be an innovative driver of complex software solutions.
- Participate in the development of complex distributed systems, including working with other engineers to help deliver the end solution.
- Describe highly technical concepts to non-technical audiences in a way they can understand.
- Hold yourself and other engineers to high standards while maintaining friendly, respectful relationships.
- Be passionate about software engineering with a strong sense of ownership for the code that you and your team write.
- Seek self-improvement and are adaptable to suggestions and feedback.
- 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. Qualifications:
- Bachelor of Science degree in Computer Engineering or Computer Science. A master’s degree or a PhD is desirable.
- 5+ years’ relevant software experience required.
- Demonstrated completion of new product design.
- Advanced experience in C and C++ programming languages is required.
- Proven experience in C programming for embedded systems, particularly at the MCU level.
- Experience in utilizing multi-threading techniques is required.
- Demonstrated use of smart pointers and modern C++ features in application development.
- Ability to interpret and create UML diagrams to communicate design intent within a team.
- Experience developing high-reliability, “mission-critical” devices and systems.
- Understanding of Continuous Delivery and Agile development.
- Experience working effectively with US teams and international teams, in both Europe and India.
- Working knowledge of software development tools such as Azure DevOps, Git, etc.
- Effective leadership, communication, and presentation skills.
- Able to work and influence in a highly cross-functional team environment.
- Excellent communication and negotiation skills, for both internal and external audiences, at all levels.
- Must travel internationally and be able to acquire all the necessary travel documents. Travel up to 10%.
- Medical device software development experience is a strong plus.
- Experience in a regulated development environment (finance, medical, defense, aerospace, etc.) is a plus.
- Experience with risk management techniques (i.e., Hazard Analysis, Risk Analysis, Failure Modes and Effects Analysis (FMEA), Fault Tree Analysis (FTA), etc., is a plus.
- Familiarity with FDA Quality Systems Regulations (QSR), ISO 62304, and EU MDR is a plus.