





Mid-level backend role at reputable medical-device employer with common tech stack and metro hiring.
Core C++/Python backend skills are transferable, but regulated medical-device V&V increases domain specificity.
Mandatory 5+ years and specific C++/Python, CMake, CI/CD, and regulated-environment familiarity.
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Design, develop, and maintain complex C++/Python applications for Linux and Windows in a regulated medical device environment.
Lead software architecture, system design, and development process improvements including build system modernization and DevOps initiatives (Docker, CI/CD pipelines).
Plan and execute verification and validation (V&V) activities ensuring compliance and quality assurance.
Bachelor’s degree in Computer Science, Software Engineering, Technical Informatics, or related field.
Minimum 5+ years of hands-on software development experience.
Strong expertise in C++ and Python programming for Linux and Windows environments.
Experience with software architecture, object-oriented design, CMake build systems, and CI/CD (Jenkins, GitLab); knowledge of DevOps and Agile environments.
Experienced in regulated or medical device software development with knowledge of SDLC, verification & validation, and compliance standards.
Proven capability in technical leadership including mentoring and coordinating cross-functional teams.
Demonstrated ability to modernize build systems and implement scalable DevOps practices integrating multi-language development environments.