Halma - Senior Firmware Engineer - Medical Devices (2-6 yrs)

EY RESPONSIBILITIES :

- Design and develop integrated software systems & firmware

- Take proof-of-concept clinical algorithms and developing them into a production worthy engine that can be deployed in end medical products

- Test/Validate and documenting as part of development process

- Collaborate with our Hardware Engineers to specify, bring up and troubleshoot new PCBAs

- Work closely with system engineers, software engineers and user experience designers to develop highly efficient and scalable algorithms that are fully compliant with appropriate medical standards

- Work with product owners to specify, estimate, break down, and author new features

- Take responsibility of the project on levels of increasing complexity

- Create and maintenance of Architecture, Requirements, design documentation and code

- Understand respiratory systems and provide sound solutions that are well researched end to end

- Capable of leading the resolution of critical bugs or incidents

- Identify and address gaps in the observability and monitoring of Systems and independently manage escalations

- Understand and make well-reasoned decisions and trade-offs within the project

- Ensure to communicate the decision at the right time to the right people and right format

- Mentor Junior team members regarding the project and sharing the best learnings

- Review documentation and authorization to sign off all related documents

SKILLS :

- BE/ME/MTech with 4+ years of experience in Firmware Development

- Prior experience in medical device development is added advantage

- Hands on Experience with ARM Cortex Microcontrollers (STM32 added advantage)

- Previous experience on Firmware development, Bootloader, Free RTOS

- In-depth understanding of Free RTOS or any other RTOS

- Strong demonstrable coding skills in C/C++ in production environments.

- Hands on experience with peripherals SPI, I2C, ADC, UART, DMA and PWM

- Experience in using tools supporting development (Analyzers, Debuggers)

- Strong testing and debugging skills

- Experience with documentation of design/development activities

- Understanding of medical devices and human respiratory system

- Experience in risk management and ISO 14971 is added advantage

- Medical device experience preferred

- Knowledge of FDA regulations and Medical Devices Directive 93/42/EEC GDP & GMP Experiences