POSITION TITLE: Senior Engineer I, Firmware
JOB LOCATION: Bangalore,India
DEPARTMENT: Firmware
REQUIRED EDUCATION: B.E from EC/EE
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 effective 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 & Good
Manufacturing Practice)