Lead Qt GUI Engineer - Medical Device Innovation

Brighter Signals

Cincinnati (OH)

On-site

USD 140,000 - 190,000

Full time

8 days ago

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Job summary

Johnson & Johnson's MedTech Surgery division in Cincinnati seeks a Lead GUI Engineer with 6+ years of C++/Qt/QML experience in a QNX environment. You will design, implement, test, and review GUI software for sophisticated medical devices and collaborate with cross-functional teams to meet regulatory requirements.

The role emphasizes hands-on development, code reviews, and leading feature development from concept through release, in a fast-paced, FDA-regulated setting.

Qualifications

  • 6+ years of software development and testing experience.
  • 5+ years GUI development using Qt/QML.
  • 5+ years of development with C++ on Linux.
  • Experience with Agile methodology and software verification.
  • Familiarity with QNX or other RTOS is preferred.

Responsibilities

  • Design, implement, and test GUI software solutions for sophisticated problems.
  • Create specifications and requirements based on clinical and user feedback.
  • Develop applications using Qt and C++ in a FDA-regulated environment.
  • Be active in design discussions and code reviews.
  • Integrate, test, and debug software solutions.
  • Lead feature development from concept through release.
  • Identify and implement improvements in architecture, design, and implementation.
  • Engage cross-functionally to discover novel solutions.

Skills

C++
Qt/QML
Linux
Agile
Unit testing
Event-driven architecture
Shell scripting

Education

BS in CS/CE or equivalent
MS or Associate degree considered

Tools

QNX

Job description

Johnson & Johnson's MedTech Surgery division in Cincinnati seeks a Lead GUI Engineer with 6+ years of C++/Qt/QML experience in a QNX environment. You will design, implement, test, and review GUI software for sophisticated medical devices and collaborate with cross-functional teams to meet regulatory requirements.

The role emphasizes hands-on development, code reviews, and leading feature development from concept through release, in a fast-paced, FDA-regulated setting.

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