Job 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\xe2\x80\x99s degree in Computer science, Electrical, Electronics / equivalent from reputed institution.

8 to 12 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++ 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

Additional Information

• Posting Date: Jan 24, 2024
• Travel: Yes,

Medtronic