Software Engineer II

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

• A Bachelor s degree in Computer science, Electrical, Electronics / equivalent from reputed institution.
• 4 to 15 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