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Warsaw, Indiana - USD Full Time Posted: Thursday, 7 December 2017
 
 
Principal Duties and Responsibilities Formulates procedures, specifications, and standards for Zimmer products and processes.
Develops and implements corrective/preventative action plans.
Collects and analyzes data for gauge and product evaluation.
Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer.
Expected Areas of Competence
Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
Ability to deliver, meet deadlines and have results orientation.
Able to communicate both orally and in written form to multiple levels of the company.
Demonstrates characteristics of high potential for future development opportunities.
Microsoft Office Suite
Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs.
Education/Experience Requirements
B. S. in engineering or an alternative Bachelor s degree program with certification as a quality engineer (e. g. CQE).
0-3 years of work experience.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred
Combination of education and experience may be considered (in evaluating experience relative to requirements)
Travel Requirements
Up to 20%


Warsaw, Indiana, United States of America
IT
USD
Zimmer Biomet
Zimmer Biomet
JS2365_9B427DDF0EDEC535C821950C7D505536/313365536
12/7/2017 7:07:39 AM

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