Senior Embedded Software Engineer (Medical Devices)

Location: Poland; hybrid work with regular office presence in Wrocław

Company

hirify.global provides engineering and technology services for software development projects.

What you will do

• Develop and maintain embedded software for medical devices used in clinical environments.
• Build and maintain embedded user interfaces with Qt/QML or Qt Widgets using C/C++.
• Work with embedded Linux and physical target hardware, including direct debugging.
• Analyze and resolve defects in a mature, large-scale codebase while optimizing performance and memory usage.
• Deliver smaller features and enhancements independently and contribute to technical decisions.
• Collaborate with customer engineering, QA, and product teams while following testing, documentation, requirements, and traceability practices.

Requirements

• 5–8 years of commercial experience in embedded software development.
• Strong C and C++ programming skills; modern C++ experience is preferred.
• Hands-on Qt experience with Qt/QML or Qt Widgets for embedded UI development.
• Solid embedded Linux experience, including debugging on target hardware.
• Strong understanding of multithreading, performance optimization, and memory optimization.
• Ability to analyze and fix defects in a large existing codebase and independently own smaller features and enhancements.
• Familiarity with Git/GitHub, CI/CD, software testing practices, and requirements or specification management tools such as Polarion or similar.
• Understanding of requirements traceability and traceability-driven development.
• Awareness of software quality practices in regulated or safety-critical environments.
• Ability to work independently, take ownership, and communicate proactively with an international customer team.
• Upper-Intermediate English (B2) or higher.

Nice to have

• Experience with Wind River Linux.
• Experience with Yocto, Buildroot, custom Linux kernels, drivers, or BSP development.
• Experience with medical device software development and/or IEC 62304.
• Experience in other safety-critical or highly regulated industries.

Culture & Benefits

• Long-term, multi-year development roadmap for a mature medical technology product.
• Hands-on work with physical devices available in the company lab.
• Collaboration with international customer engineering, QA, and product teams.
• Hybrid work model with regular office presence in Wrocław.
• Equal opportunity employment.

Hiring process

• Complete the application form; the recruiting team will follow up.