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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.

· 4 to 8 years’ experience in Embedded Software development with at least four (2) years’ experience in the Medical device/Medical IT or regulated industry.

· Expertise in modern C++ 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

About Medtronic

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives.Help us shape the

future.

Whatever your specialty or ambitions, you can make a difference at Medtronic - both in the lives of others and your career. Join us in our commitment to take healthcare Further, Together.

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It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.