Principal Software Engineer /Embedded C++ Developer

Job Description:

• Work with global R&D teams to develop software for new and existing medical device products.
  • Software design and development of embedded real-time systems, including the development of Software Unit Test & Integration plans and protocols.
  • Participates in reviews, code inspections and will support the development of documentation required for FDA device approval.
  • Work effectively within a geographically dispersed and cross-functional teams during all phases of the product development process.
  • Develop test automation framework and test scripts.
  • Must be responsive, flexible, self-motivated and able to succeed within an open collaborative peer environment
  • Is highly effective, agile and thrives in a dynamic environment with multiple, changing priorities
  • Is comfortable with proactive outward communication and never shies away from a challenge
  • Be Agile and effectively navigate through changing project priorities.
  • Mentor, guide and train other engineers

Must Have--Minimum Qualification

• A Bachelor’s degree in Computer science, Electrical, Electronics / equivalent from reputed institution.
• 3 to 16 years’ experience in Embedded Software development with at least four (4) years’ experience in the Medical device/Medical IT or regulated industry.
• Expertise in modern C++ (C++ 11 and above) software design & coding required in an Embedded development environment.
• Expertise of Object-Oriented Analysis & Design (OOAD) and familiarity with UML is strongly desired.
• Know-how in field-bus technology (EtherCAT preferred) and standard embedded communication protocols (DDS, SPI, I2C, AXI, UART, etc.)
• Desired experience with RTOS like Linux/WinCE/ThreadX etc with multi-threading, IPC knowledge.
• Experience in hardware/software interfacing and design issues. Analyze unexpected, undesirable, or non-understood behavior in software and in interactions of software with hardware.
• Experience working in a structured software development environment following a well-defined software development process like Agile / Lean.
• Experience with software risk analysis (per ISO 14971) including software failure mode and effects analysis (FMEA).
• Strong analytical skills and ability to multi-task.
• Superior written and verbal communication skills required.
• Strong interpersonal, presentation, and organizational skills.
• Awareness of Medical Device standards IEC 60601-1, IEC 62304, ISO 13485, ISO 14971 and applicable FDA standards