Senior Software Engineer — Medical Device Impact

Lumicity; San Francisco (CA); Sur place; USD 140 000 - 200 000; Plein temps

Résumé du poste

Lumicity in San Francisco, CA is seeking an experienced Software Engineer to design, build, and test software for a regulated medical device. You will own features from requirements through verification and collaborate with hardware, systems, and QA teams to ensure compliance and patient safety.

You have 3+ years of professional software development in C++, C#, or Python, and familiarity with IEC 62304, ISO 13485, or FDA design controls.

Qualifications

• BS or MS in Computer Science, Software Engineering, Electrical Engineering, or a related field.
• 3+ years of professional software development experience in C++, C#, or Python.
• Experience working in a regulated environment (medical device, aerospace, or similar).
• Familiarity with IEC 62304, ISO 13485, or FDA design controls.
• Strong communication skills and a collaborative approach.

Responsabilités

• Design, develop, and test production-quality software for a medical device platform.
• Write clear requirements, design documentation, and verification tests that support regulatory submissions.
• Collaborate with cross-functional teams to integrate software with hardware and system components.
• Troubleshoot issues, perform root cause analysis, and drive continuous improvement.
• Participate in code reviews and help raise the bar on engineering best practices.

Connaissances

C++

C#

Python

Formation

BS or MS in Computer Science, Software Engineering, Electrical Engineering, or a related field

Description du poste

Lumicity in San Francisco, CA is seeking an experienced Software Engineer to design, build, and test software for a regulated medical device. You will own features from requirements through verification and collaborate with hardware, systems, and QA teams to ensure compliance and patient safety.

You have 3+ years of professional software development in C++, C#, or Python, and familiarity with IEC 62304, ISO 13485, or FDA design controls.