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Zimmer Biomet seeks a Quality Engineer to assure product conformity through audits, inspections, and testing. You will interact with various departments, suppliers, and external experts to meet Zimmer Biomet quality goals.
Responsibilities include developing procedures, corrective actions, data analysis, and ensuring suppliers have the necessary information to deliver quality products. The role requires teamwork, meeting deadlines, and clear communication across levels.
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
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.
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
Proficient in blueprint reading and geometric dimensioning and tolerancing, thorough 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).
Minimum 1 year of relevant work experience.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred
20%
EOE/M/F/Vet/Disability