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

Our Global Quality Strategy is rooted in the Medtronic Mission and our Quality Policy. Being a 'trusted partner' means always putting patient safety first, upholding product quality, and maintaining the highest ethical standards in our business relationships and programs.

This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.

As an Associate Quality Systems Specialist you will be a focal point for the processing and initiation of changes to documentation that is directly related to our products and to the Quality Management System vital to our medical devices.

Responsibilities may include the following and other duties may be assigned.

• Process change orders and prepares for change authorization and documentation.
• Maintain functional control of product Master Data, document change control and Quality System records.
• Review and analyze engineering change data and coordinate changes with various departments including engineering, quality, manufacturing, etc.
• Analyze proposed changes of product design to determine effect on overall product and system.
• Ensures that customer requirements are implemented, and reviews change accounting activity to ensure compliance with quality management policies.

Required Knowledge and Experience:

• Quality management or document control experience
• Working knowledge of Microsoft Office tools, desktop publishing software experience (Microsoft Office Suite, Adobe Acrobat)
• Familiar with modern Enterprise Resource Planning (ERP), Product Lifecycle Management (PLM) systems, and manufacturing documentation (i.e. Bill of Materials, item masters, Design History File, Device Master Record, etc.)

• Excellent communication skills- oral and written.
• Able to work independently and within a team
• Bachelor's Degree within 1-2 years of experience in quality. Candidates from a regulated industry will be preferred

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 95,000+ 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.