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Senior Software Engineer - Embedded C++ , OS, I2C,SPI,UDP,DDS - (230004QX)
Description
A Day in the Life
· 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
Qualifications
Minimum Qualification
· A Bachelor’s degree in Computer science, Electrical, Electronics / equivalent from reputed institution.
· 4 to 12 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
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