ResponsibilitiesServe as a technical expert for embedded software design activities contributing to product development and research applications across physiologic monitoring systems and subsystems, such as pulse oximetry, regional oximetry, EEG based devices, and other sensing technologies.Influence software technical direction, design patterns, and architectural standards aligned with system requirements and long‑term platform strategies.Collaborate closely with systems, hardware, algorithm, and test engineering partners, translating complex clinical and system requirements into robust, real‑time embedded software solutions.Translate clinical, system, and regulatory requirements into reliable, real‑time embedded software solutions.Collaborate cross‑functionally with systems, hardware, algorithm, test, and quality engineers to ensure cohesive and testable product designs.Provide hands‑on technical leadership for implementation of critical software components, including real‑time operating systems, device drivers, middleware, and application logic.Review software designs, code, and test results to ensure robustness, performance, safety, and maintainability.Serve as a technical authority for embedded software, resolving complex, ambiguous, or cross‑cutting technical issues.Mentor and technically guide engineers through design reviews, code reviews, and problem‑solving activities without formal people management responsibilities.Promote best practices for embedded software development, including coding standards, version control, documentation, and secure development practices.QualificationsDeep expertise in embedded software architecture and development for real‑time, safety‑critical systems, including strong proficiency in C/C++ and embedded development tools.Extensive experience working with real‑time operating systems (RTOS), device drivers, middleware, and low‑level hardware interfaces.Proven ability to define software architecture, design patterns, and technical direction for complex embedded systems and platforms.Experience with digital signal processing for physiologic signals preferred.Experience with hardware description language and configurable hardware preferred.Experience implementing machine learning inference architectures optimized for embedded environments preferred.Experience developing software for regulated products; familiarity with IEC 62304 medical device software lifecycle practices and standards preferred.Experience collaborating closely with hardware, systems, algorithm, and test engineers to deliver integrated, high‑quality solutions.Demonstrated ability to resolve complex, ambiguous, or cross‑cutting technical challenges spanning multiple subsystems.Proficiency with version control, configuration management, and continuous integration practices in embedded environments.Excellent communication skills, with the ability to explain complex technical concepts and tradeoffs to diverse technical and non‑technical stakeholders.Physical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.Benefits & CompensationCompensation includes a base salary of 83,520.00 EUR to 125,280.00 EUR (Ireland) and eligibility for the Medtronic Incentive Plan (MIP). Additional benefits include a flexible benefits package and resources designed to support employees at every career and life stage.
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