Software Engineer II

Must Have

Minimum Qualifications

·         B.E or B.Tech in Computer Sciences, Electronics or Electrical Engineer..

·         4+ years of experience in software design and development is required.

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

·         Experience in embedded Linux and real-time applications required

·         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, Security

·         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 desirable

·         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 skills.  

·         Excellent time management and professionalism   

·         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.

Nice to Haves

·         M.S or M.Tech with 2+ years of experience in software design and development is preferred.

·         Experience in real-time applications is preferred.

·         Medical instrument development experiences a plus.

·         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

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.