Posted in Architecture 30+ days ago.
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Location: Warsaw, Indiana
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.
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. Performs supplier Desktop Assessments and Supplier Onsite Audits. Assesses and determines validation and verification requirements for Supplier Change Notifications, and drive the Supplier Change Notifications to completion. Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer.
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.
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)
Up to 20%