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A Day in the Life
Work in a cross-functional Agile and global R&D teams to develop software for new and existing medical device products.
Design software for a robotic minimally invasive surgery system, utilizing object-oriented software design principles and other best practices.
Participate in the documentation of the software, including architecture and design detail, unit testing, test statergy, anomaly tracking and reports.
Software design and development of embedded real-time systems, including the development of Software Unit Test & Integration plans and protocols.
Software development for product testability.
Uses static analysis tools to identify and address potential defects.
Analyze unexpected, undesirable, or non-understood behavior in software and in interactions of software with hardware.
Participates in other quality assurance functions, including, but not limited to, static code analysis, risk/hazard analysis, and test automation development.
Meet key business KPI/project metrices.
Hire and mentor junior colleagues and peers.
Must Have
Minimum Qualification
A Bachelor\xe2\x80\x99s degree in Computer science, Electrical, Electronics / equivalent from reputed institution.
12 to 20 years\xe2\x80\x99 experience in Embedded Software development with at least four (4) years\xe2\x80\x99 experience in the Medical device/Medical IT or regulated industry.
Expertise in modern C++ (C++ 14 and above) software design & coding required in an Embedded development environment.
Expertise of Object-Oriented Analysis & Design (OOAD) and familiarity with UML / SysML 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/QNX etc with multi-threading, IPC knowledge.
Experience in hardware/software interfacing and design issues.
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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