Position Details
About this role
Design, develop, and maintain software for safety-critical medical devices, ensuring compliance with regulatory standards. Lead technical efforts and mentor engineering teams in a regulated environment.
Key Responsibilities
- Lead software design and implementation
- Ensure regulatory compliance
- Support risk management activities
- Mentor engineers
- Participate in design reviews
Technical Overview
Embedded software development using C, C++, Linux, Qt/QML, with focus on medical device standards IEC 62304 and ISO 14971, in a regulated environment.
Ideal Candidate
The ideal candidate is a mid-level embedded software engineer with 4+ years of experience in medical device software development, proficient in C, C++, Linux, and Qt/QML. They should have strong leadership skills and experience working in regulated environments.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Certifications
Preferred
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of embedded systems experience, No experience with medical device regulations, Inability to work in a hybrid environment
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