Senior Software Engineer

Lumicity; San Francisco (CA); Presencial; USD 140 000 - 200 000; Tempo integral

Resumo da oferta

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.

Qualificações

• 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.

Responsabilidades

• 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.

Conhecimentos

C++

C#

Python

Formação académica

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

Descrição da oferta de emprego

Our client is a growing medical device company building technology that improves patient outcomes. The team is collaborative, mission-driven, and moving from development into the next stage of growth. This is a chance to see your code make a real difference in patients' lives.

About the role

You'll design, build, and test software for a regulated medical device, working closely with systems, electrical, mechanical, and quality engineers. You'll own features from requirements through verification and help shape how the software is developed as the team scales.

What you'll do

• 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

What we're looking for

• 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

Nice to have

• Embedded software or real-time systems experience
• Experience with cybersecurity, risk management (ISO 14971), or software verification and validation
• Background in medical devices, signal processing, or algorithm development