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 talented 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 inspired, invested, cared for, valued, and have a strong sense of belonging. Requirements Responsible for executing product failure root cause investigations according to global requirements to drive product and regulatory compliance, while ensuring 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. Supports product development and new product introduction, ensuring compliance with design control and risk management regulations and standards. Perform root cause investigations to drive product improvement and quality. Formulates procedures, specifications, and standards for Zimmer products and processes. Develops and implements corrective/preventative action plans. Activities will include, but are not limited to: Complaint evaluation and investigation. The writing and filing of Medical Device & Vigilance Reports. Tracking and trending of product quality. Identification, execution, and closure of remedial actions. Other complaint handling activities for the global enterprise in compliance with applicable regulations and guidance requirements worldwide. Coordinate and lead supplier quality activities: Supplier Corrective Action. Supplier Change Notification. Supplier Production Part Approval. Supplier NCRs. Ensure site KPIs are met. English proficiency is required (B2-C1). Please note that you must submit your resume in English at the time of applying, or your application will not be considered. 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. Microsoft Office Suite knowledge. Proficient in blueprint reading and geometric dimensioning and tolerancing, thorough understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods. Your Background B.S. in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE). 3 -5 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 Expectations Up to 20% EOE/M/F/Vet/Disability