Associate quality systems specialistMedtronic Cardiac and Vascular

Job Description
Careers That Change Lives
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.
A Day in the Life
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.
Must Haves
< span>Bachelor's Degree within 1-2 years of experience in quality. Candidates from a regulated industry will be preferred
Your Profile:
Quality management or document control experience
Working knowledge of Microsoft Office tools, desktop publishing software experience (Microsoft Office Suite, Adobe Acrobat)
Familiar with modern ERP systems, PLM systems and manufacturing documentation (i.e. BOMs, item masters, DHF, DMR, etc.)
Excellent communication skills- oral and written.
Able to work independently and within a team