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

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

• Process change orders and provide guidance in change order process in compliance with applicable procedures that support compliance with regulations and standards pertaining to medical device quality system change management.

• Work with change originators to maintain clear, concise and valid documents throughout.

• Process parts and documents changes in a timely manner according to requirements and procedures to support business requirements.

• Drive and facilitate in a timely manner the change, approval and release of documentation according to project schedules, including the resolution of resource issues relative to the processing of document change orders.

• Responsible for data entry integrity when transferring changes to product data in multiple systems.

• Responsible for ensuring that the best practices of Part/Document Change Management are followed.

• Monitor parts and documents changes management process effectiveness and contribute to problem solving/continual improvement discussions regarding change control process, including the impact of changes

• Participate in department meetings and performs other tasks and related duties as assigned.

Required Knowledge and Experience:

• Bachelor’s Degree required

• Minimum of 2 years related experience

• Proficient using the following software systems: Agile and SAP.

• Skilled in tasks associated with document handling, archiving and change management.

• Excellent analytical, verbal communication and writing skills.

• Ability to work in a team environment as well as independently

• Exhibits high degree of initiative and good judgment.

• Knowledge in using Agile PLM Import Tool and competent in Agile searches is preferred

• Knowledge of product design and assembly to make informed decisions about quality management so that the documentation is efficient and complete.

• Experience in the manufacture and development of product, preferably medical devices.

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.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

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.

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