• Develop firmware for bare-metal C++ applications (e.g., Silicon Labs chips) and embedded Linux platforms
• Perform schematic design, PCB layout, and prototype testing
• Translate user requirements into clinical and technical specifications
• Maintain detailed design documentation, test plans, and regulatory compliance records
• Collaborate with cross-functional teams including R&D, regulatory, manufacturing, and clinical partners
• Work with contractors, suppliers, and integration partners to ensure successful product delivery
• Investigate real-world device faults and support customer issue resolution
• Conduct site visits, including clinical theatres, and engage directly with anesthesiologists and end-users
• Drive innovation and contribute to continuous improvement of product design and manufacturing workflows

Technical Skills: 

• Embedded C/C++ development (bare-metal and RTOS)
• Embedded Linux development and system-level debugging
• Strong understanding of analogue and digital circuit design
• PCB schematic capture and layout
• Hardware debugging using oscilloscopes and other lab equipment
• Working knowledge of communication protocols including UART, SPI, I2C, TCP/IP, and Bluetooth
• Experience using version control systems (Git)

Qualifications:

• Bachelor’s degree in Electronic or Electrical Engineering
• 1+ years of hands-on experience in embedded systems, firmware development, and electronics design

• Team Leadership: Lead, mentor, and manage a team of software and firmware engineers, guiding technical output and fostering a culture of engineering excellence.
• System Architecture: Drive end-to-end system design across the technology stack, ensuring seamless integration between embedded firmware, mobile applications, and cloud environments.
• Engineering Quality: Conduct thorough reviews of system designs, architecture documentation, and pull requests to ensure performance, security, and scalability standards are met.
• Full Lifecycle Ownership: Oversee complex software and connected medical products from concept and specification through prototyping, validation, production, and post-market improvements.
• Regulatory Compliance: Ensure all software design and architecture complies with medical device standards (ISO 13485, IEC 60601, IEC 62304) and cyber risk assessment protocols.
• Cross-Functional Collaboration: Partner closely with hardware engineering and R&D leadership to align software capabilities with hardware co-design objectives.

Qualifications & Experience: