Senior Software Engineer-C++ QT QML

Job Summary

• Develop and maintain software components using C++, Qt, and QML for core modules, user interfaces, and device interfaces.
• Translate clinical, regulatory, and product requirements into scalable and maintainable software implementations.
• Implement established design patterns, componentization, interfaces, and data models.
• Participate in software design and technical reviews and contribute to architectural decisions and trade-offs.
• Ensure software implementation is traceable to requirements and supports risk management and safety-related design activities.
• Develop software in compliance with medical device regulations and software lifecycle processes, including ISO 13485, IEC 60601-1, and MDR/IVDR as applicable.
• Consider safety, reliability, performance, cybersecurity, and fail-safe behavior during software development.
• Develop and integrate software components for hardware-software integration, drivers, middleware, real-time constraints, and platform portability.
• Perform code reviews and ensure effective code quality, testing, and software design documentation.
• Collaborate with UX/UI, QA, regulatory, hardware, and clinical teams to align software implementation with user needs and validation plans.
• Develop and maintain software design artifacts, component documentation, interface specifications, NFRs, and API specifications.
• Identify and communicate technical risks and contribute to mitigation plans, reuse strategies, and platformization where feasible.

Required Qualifications

• Bachelors or Master’s degree in Computer Science, Software Engineering, or related field.
• 5+ years of professional software engineering experience in C++ with strong object-oriented and design-pattern skills.
• Experience developing software using Qt (Widgets or QML) for complex, user-centric desktop or embedded UI.
• Strong understanding of cross-platform development, performance optimization, memory management, and real-time considerations.
• Familiarity with hardware/firmware integration, device drivers, and IPC mechanisms.
• Solid knowledge of the software development lifecycle in regulated environments, including requirements, design, implementation, verification, validation, and change control.
• Experience with risk management processes (ISO 14971) and software safety concepts.
• Strong communication and collaboration skills with the ability to work effectively across disciplines.

Nice-to-Haves

• Experience with embedded Linux, real-time OS, or bare-metal environments.
• Knowledge of cybersecurity standards and secure-by-design practices for medical devices.
• Experience with formal methods or model-based design, including UML, SysML, or architecture frameworks.
• Fluency in additional languages used in healthcare, such as German or French, or knowledge of global regulatory requirements.
• Prior experience in a compliance/audit context and successful regulatory submissions.

Technical Skills

• C++ (C++11/14/17/20), modern idioms, templates, RAII, STL, move semantics.
• Qt framework: Widgets, signals/slots, QML, model-view patterns, MVC/MVVM.
• Software architecture styles: layered, component-based, event-driven, service-oriented.
• APIs, SDKs, middleware, and hardware abstraction layers.
• Software design and modeling using UML/SysML and architecture documentation.
• Version control, CI/CD, test automation, and code quality tooling.
• Knowledge of standards: IEC 62304, ISO 62366, ISO 14971, ISO 13485.

Responsibilities (Regulatory and Quality)

• Ensure software design and development documentation supports regulatory submissions and audits.
• Maintain requirements traceability and provide evidence for verification and validation.
• Collaborate with cybersecurity, safety, and quality teams to meet regulatory expectations.
• Ensure software development activities follow defined quality and software lifecycle processes.
• Support identification and mitigation of software-related risks.
• Ensure software implementation meets defined safety, reliability, performance, and quality requirements.