21 Mar

Software Engineer - Hyderabad - Medtronic

Software Engineer
Hyderabad AP
21 Mar, 2017 9 days ago

Medtronic as the company that open the jobs vacancy, have some qualification and spesification especially for the Software Engineer jobs vacancy. To find out more information and about qualification and spesification details, walkin interview schedule, the address of the company, the company contact info (email/phone number) of Medtronic company, please start to apply for the job vacancy with fill the jobs application with click the 'Apply This Job' button below.

Position Overview

Medtronic is the world’s largest medical technology company,
offering an unprecedented breadth and depth of innovative therapies to fulfill
our Mission of alleviating pain, restoring health, and extending life.


The Senior Software Engineer, Embedded Software will
be a member of the Medtronic R&D software team working on new development
and support of electro surgery generator products. Senior Software
Engineer are considered experts in embedded software development including the
understanding of how software interacts with hardware and FPGAs. The position
is a hands-on development role with a dynamic set of responsibilities in a
complex software system including coding applications, user interfaces,
drivers, and utilizing various middleware and frameworks. The Senior Software
Engineer, Platform Software will be a member of the Medtronic R&D
engineering, Hyderabad team working on the development and support of Medtronic
next generation minimally invasive platform.


Must be a team player. Must have
qualities including being positive, high standards, resilient, open, and

Takes pride in quality, extensible, and maintainable
work products. Demonstrates excellent coding practices.

Commitment to achieving and exceeding project goals
and timelines.

Thrives in working with other disciplines to develop
system-minded implementations that take into account safety, performance,
communication, user interface and other aspects of a final product.


Education :
BS degree in CS, EE or
equivalent. MS EE/CS preferred.

BS with 8 to 12 years of experience in
software design and development is required.

MS with 6 to 10 years of experience in
software design and development is preferred.

Experience in real-time applications is

Medical instrument development experiences a

Expertise in C/C++ required in an Embedded
Linux, RTOS development environment.

Experience in embedded Linux or any RTOS

Knowledge of OOA&D and familiarity with
UML is strongly desired.

Experience in hardware/software interfacing
and design issues required.

Superior written and verbal communication
skills required.

Desired experience with Qt, SQLite, Linux Yocto,

Strong interpersonal, presentation, and
organizational skills

Participate in System design, coordination
with teams and internal product management

Working knowledge of networking protocols.

Hands on experience in Embedded / Firmware
Device Driver

Awareness on wireless technology is highly

Experience in medical device SW development is
added advantage

Ability to define, develop and implement
automated unit / integration test solutions

Experience with change control, requirements
management, source code control

Excellent verbal and written communication

Excellent time management and

Perform Code Reviews , Static Code Analysis ,
Dynamic Code Analysis

Generate Software Metrics for Unit Testing,
Integration Testing

Works collaboratively with software engineers,
and SW QA.


Preferred Skills:
Appreciation of discipline and work required
to develop software in a regulated industry

Familiarity with FDA Quality System
Regulations (820.30 design controls), European Regulatory Requirements (ISO
13485), and specifically IEC62304 is preferred.

Demonstrates knowledge and understanding of
standards and guidance’s relevant to the medical device industry


Reports to the Software Manager for functional leadership.

Frequent interaction with team members from other disciplines,
particularly hardware engineers, to develop project requirements and other
project artifacts such as project schedules. Possible interaction with clinicians,
third-party vendors, manufacturers, subcontractors and other users.

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