Job ID: JOB_ID_3877
Job Description:
We are looking for an experienced Embedded Software Engineer with a Bachelor’s or Master’s degree in Computer Science, Electrical Engineering, or a related field. This role requires 8+ years of professional software development experience, with a preference for experience in the medical device or regulated industry. The engineer will work with electro-pneumatic or electromechanical devices, focusing on interfaces with actuators, sensors, and fluid or flow control systems.
Key Responsibilities:
- Develop embedded software for microcontroller-based systems (e.g., STM32, NXP, TI).
- Work with communication protocols such as UART, SPI, I2C, and CAN.
- Implement unit testing, static analysis, code reviews, and system integration testing within a structured SDLC environment.
- Develop and document embedded software for FDA-regulated Class B and Class C medical devices.
- Ensure compliance with relevant standards including IEC 62304 (software life cycle), ISO 14971 (risk management), and FDA medical device software guidance.
Required Skills:
- Bachelors or masters degree in computer science, Electrical Engineering, or a related field.
- 8+ years of professional software development experience, preferably in the medical device or regulated industry.
- Experience working with electro-pneumatic or electromechanical devices involving interfaces with actuators, sensors, and fluid or flow control systems.
- Experience developing embedded software for microcontroller-based systems (e.g., STM32, NXP, TI).
- Experience working with communication protocols such as UART, SPI, I2C, and CAN.
- Experience with unit testing, static analysis, code reviews, and system integration testing in a structured SDLC environment.
- Practical experience developing and documenting embedded software for FDA-regulated Class B and Class C medical device software.
- Working knowledge of relevant standards including IEC 62304 (software life cycle), ISO 14971 (risk management), and FDA medical device software guidance.
Keywords:
C programming, information technology, California
Special Requirements
FDA-regulated Class B and Class C medical device software development experience. Experience with IEC 62304, ISO 14971, and FDA medical device software guidance.
Compensation & Location
Salary: $65 – $80 per year (Estimated)
Location: Irvine, CA
Recruiter / Company – Contact Information
Recruiter / Employer: Concord it systems
Email: .steve@concorditsystems.com
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