Senior Software QA Engineer - Remote Embedded Medical

Dexcom, Inc.; California; A distancia; USD 96.000 - 160.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits

Career development

Tuition reimbursement

Global opportunities

Descripción de la vacante

Dexcom is seeking a Software QA Engineer to join our embedded systems team in San Diego. You will ensure compliance with medical device regulations and lead QA activities across the software lifecycle, partnering with firmware and algorithm teams to deliver high‑quality CGM software.

Ideal candidates have 5–8 years of relevant experience in regulated environments, strong testing and risk management skills, and a hands‑on approach to design reviews and validation.

Formación

• Bachelor’s degree in a technical discipline is typically required.
• 5–8 years of related experience, or a Master’s with 2–5 years, or PhD with 0–2 years.
• Experience in software quality or engineering across requirements, design, integration, and testing.
• Experience in regulated environments (medical devices) and design controls.

Responsabilidades

• Ensure compliance with IEC 62304, 21 CFR Part 820 and global regulations.
• Deliver high‑quality embedded software for medical devices with cross‑functional teams.
• Lead and participate in design reviews, requirements analysis, and risk management.
• Oversee software design controls, testing, configuration management, and validation.
• Participate in pre‑market and post‑market activities and CAPA processes.
• Contribute to verification and validation across the SDLC with risk-based testing.

Conocimientos

Software QA

Embedded systems

Firmware

Regulatory compliance

SDLC processes

Cross-functional collaboration

Testing

Educación

Bachelor’s degree in technical field

Master’s degree preferred

Herramientas

Jama

CI/CD pipelines

RTOS familiarity

Descripción del empleo

Dexcom is seeking a Software QA Engineer to join our embedded systems team in San Diego. You will ensure compliance with medical device regulations and lead QA activities across the software lifecycle, partnering with firmware and algorithm teams to deliver high‑quality CGM software.

Ideal candidates have 5–8 years of relevant experience in regulated environments, strong testing and risk management skills, and a hands‑on approach to design reviews and validation.