Sr Software Engineer - Hyderabad, India - Medtronic
Description
Careers that Change Lives
The Senior Software Engineer will be responsible for software design and development activities of complex electro-mechanical medical devices.The engineer will be a part of a small but a highly professional and geographically distributed Software team.
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
Must Have
Minimum Qualification
·A Bachelor's degree in Computer science, Electrical, Electronics / equivalent from reputed institution.
·8 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 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 , IEC 62304, ISO 13485, ISO 14971 and applicable FDA standards
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