KEY RESPONSIBILITIES: • Designing and developing integrated software systems & firmware for medical devices
- Taking proof-of-concept clinical algorithms and developing them into a production worthy engine that can be deployed in end medical products
- Testing/Validating and documenting as part of development process
- Collaborate with our Hardware Engineers to specify, bring up and troubleshoot new PCBAs
- Working 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
- Taking 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
- Mentoring Junior team members regarding the project and sharing the best learnings
- Reviewing documentation and authorised to sign off all his related documents
SKILLS &
RESPONSIBILITIES
- B.E from EC/EEE with hands on experience of 4+ years 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
- 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 (Good Documentation Practice & Valuable