Software Engineer III

About the Role

Key Responsibilities

• 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 and 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.
• Mentor junior engineers to help them grow technically and professionally.
• Work with Software Architects to define designs and workflows.
• Ensure consistency across teams and integrate with other teams.
• Ideate and drive complex software solutions.
• Participate in the development of complex distributed systems.
• Describe highly technical concepts to non-technical audiences.
• Hold high standards while maintaining respectful relationships.
• Demonstrate ownership and passion for software engineering.
• Seek self-improvement and be adaptable to feedback.
• Uphold the company's core values and Code of Ethics and Conduct.

Requirements

• Bachelor of Science degree in Computer Engineering or Computer Science; a master's degree or PhD is desirable.
• 5+ years' relevant software experience.
• Demonstrated experience in new product design.
• Advanced experience in C and C++ programming languages.
• Proven experience in C programming for embedded systems, particularly at the MCU level.
• Experience in utilizing multi-threading techniques.
• Use of smart pointers and modern C++ features in application development.
• Ability to interpret and create UML diagrams.
• Experience developing high-reliability, mission-critical devices and systems.
• Understanding of Continuous Delivery and Agile development.
• Experience working with US and international teams.
• Working knowledge of software development tools such as Azure DevOps, Git.
• Effective leadership, communication, and presentation skills.
• Ability to influence in a highly cross-functional team environment.
• Willingness to travel internationally up to 10%.
• Medical device software development experience is a strong plus.
• Experience in regulated development environments (medical, defense, aerospace, etc.) is a plus.
• Experience with risk management techniques (FMEA, FTA, Hazard Analysis, etc.) is a plus.
• Familiarity with FDA QSR, ISO 62304, and EU MDR is a plus.

Nice to Have

• Experience in medical device software development.
• Experience in regulated development environments such as finance, defense, aerospace.
• Knowledge of risk management techniques like FMEA, FTA.
• Familiarity with FDA Quality Systems Regulations (QSR), ISO 62304, and EU MDR.

Qualifications

• Bachelor of Science in Computer Engineering or Computer Science.
• 5+ years of relevant software experience.

Benefits & Perks

• Please review our benefits at Life at OSI. The specific programs and options vary depending on eligibility, location, and hire date.
• Salary is based on candidate experience, qualifications, market, and business considerations.