Software Engineer

Company Description: Terumo Blood and Cell Technologies, headquartered in Lakewood, Colorado, is a global leader in blood component, therapeutic apheresis, and cellular technologies, serving customers in more than 160 countries. With a unique portfolio spanning apheresis collections, whole blood processing, and pathogen reduction, the company focuses on unlocking the potential of blood and cells to improve patient outcomes. Since its origins in 1964 as COBE Laboratories, nearly 7,900 associates worldwide have been committed to advancing health care and acting as conscientious corporate citizens with social, environmental, and economic responsibility. The organization emphasizes continuous discovery, innovation, and collaboration, supporting education and research through community involvement and grants. Terumo Blood and Cell Technologies offers diverse career opportunities across R&D, IT, engineering, clinical sciences, manufacturing, software development, and quality and regulatory functions.
Role Description This is a full-time, Software Quality Engineer role based in Costa Rica. The Software Engineer will design, develop, test, and maintain software solutions that support blood and cellular technologies, ensuring reliability, safety, and regulatory compliance. Daily responsibilities include collaborating with cross-functional teams to gather requirements, creating technical specifications, implementing and reviewing code, and participating in design and architecture discussions. The role also involves troubleshooting and resolving software defects, writing automated tests, and contributing to continuous improvement of development processes and tools. The engineer will work closely with quality, regulatory, and product teams to deliver solutions that meet customer needs and enhance patient outcomes.
Requirements:3+ years of software development experience.Strong experience with C#/.NET, Angular, and SQL Server.Experience developing software for Medical Devices or SaMD.Experience working under IEC 62304 and/or ISO 13485.Hands-on experience with Verification & Validation (V&V), validation documentation, and requirements traceability.Strong software design and problem-solving skills.Bachelor’s degree in Computer Science, Software Engineering, or related technical field; advanced degree or relevant certifications are a plus.English proficiency (written and spoken) sufficient for technical documentation, collaboration, and meetings; additional language skills are beneficial.Interest in healthcare innovation and commitment to contributing to solutions that positively impact patients and clinical outcomes
Nice to Have:ISO 14971FDA-regulated productsDesign ControlsRisk Management
Join our R&D team to build innovative healthcare solutions that improve patient outcomes while meeting the highest quality and regulatory standards.