Quality Assurance Engineer At Zimmer Biomet, we push the boundaries of innovation and drive 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 recognized. Key Responsibilities: - Assure products conform to established requirements and standards through appropriate audit, inspection, and test activities. - Interact with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. Impact You'll Create: - Help with different supplier functionalities and project manage. - Formulate procedures, specifications, and standards for Zimmer products and processes. - Develop and implement corrective/preventative action plans. - Collect and analyze data for gauge and product evaluation. - Maintain critical gauges, procedures, and materials needed to maintain existing products. - Ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet. What Makes You Stand Out: - 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. - Proficient in 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. - Ability to use optical comparators and CMMs. Requirements: - English proficiency required (C1). - B.S. in Engineering. - Minimum 3 years of relevant work experience. - Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred. Travel Expectations: - Up to 5%.