https://bayt.page.link/NoxeEwydRBEzHbRq8
أنشئ تنبيهًا وظيفيًا للوظائف المشابهة

الوصف الوظيفي

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.


A Day in the Life

The Principal Software Test Engineer, based in Hyderabad, India, is responsible for various software Quality Assurance functions during the development lifecycle of complex electro-mechanical medical devices.


A Day in the Life


The Principal Software V&V, based in Hyderabad, India, is responsible for ensuring that developed software meets and complies with defined or standardized quality specifications throughout the software development life cycle (SDLC) of complex electro-mechanical medical devices.


The individual will be a part of a small but professional Software Quality Assurance team and will work closely with Software development engineers and other cross functional teams


This position is participating in development of Automation strategies, test strategies, test plans and test procedures of various software platforms (i.e. embedded, real-time OS, Client-server, web-based, etc.).


The individual will report to the Emgineer Manager and be a part of a SWQA project team that may consist of on and offsite resources and will work closely with software developers and other cross functional team members.


Must Have


Job Responsibilities


  • Architect, Develop and execute Embedded software Test Automation Statergy/ Frameworks/Platforms for Medical Devices accross Medical Surgical Group in Collobration with Cross Functional teams like Elecrtical, Mechanical etc.
  • Develop & Deliver CI/CD plans for Embedded Automation Test Suites
  • Plan, Develop and execute software testing (both manual and automated – White/Black Box) for Embedded medical devices, based on context and risks associated with the project.
  • Participate in some level of basic software design reviews and documentation that establish high level of confident that the software development meets the required quality parameters.
  • Participate in test activities, incident management and tracking – with both on or offsite test resources.
  • Flexibel to move across projects based on Priority and Business needs
  • Create test reports suitable for submission to regulatory authorities to demonstrate that software is validated, and all requirements are verified.
  • Responsible for ensuring that the software development process follows established procedures, standards and plans. And the risk associated with the software is identified, analyzed and managed appropriately.
  • Participate in other quality assurance functions, including, but not limited to, supporting compliance audits, test automation strategy and development.
  • Active Participation in team meetings, discussions and customer meetings.
  • Involvement in Innovation, technical discussion’s, product/process improvements and Kaizans.

Minimum Qualifications & Specialized Knowledge required


  • ME/MTech/BE/BTech in Electronics & Communication Engineering, Computer Science or relevant field.
  • A 14+ years in Embedded software quality assurance, with atleast 4 to 5+ years experience in Developing Embedded Test Automation Architectures
  • Or, some medical device product experience (preferably electro-mechanical medical device) or regulated fields.
  • Experience in CI/CD modles like Bamboo, Jenkins etc is preferred.
  • Proficient in Automation languages (e.g. Python..)
  • Some working experience in a prescriptive software development environment following a well-defined software development process.
  • Excellent verbal and written communication skills and works well in a tightly coupled team

Nice to Haves


  • Experience with test equipment such as oscilloscopes, serial port analyzers, multi-meters and general lab measurement equipment.
  • Membership in one or more professional societies and/or professional certification (e.g. CSQE, CSTE, etc.). 
  • Familiarity with FDA regulations and recommended practices regarding software (21CFR 820.30, IEC 62304:2015, ISO 14971:2012).
  • Understand Requirements Management, configuration management and defect tracking concepts.

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.
 


Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 


Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
 


About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.


Learn more about our business, mission, and our commitment to diversity here  
 


لقد تجاوزت الحد الأقصى لعدد التنبيهات الوظيفية المسموح بإضافتها والذي يبلغ 15. يرجى حذف إحدى التنبيهات الوظيفية الحالية لإضافة تنبيه جديد
تم إنشاء تنبيه للوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.
تم إلغاء تفعيل تنبيه الوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.