JOB DESCRIPTION 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 recognized.What You Can ExpectResponsible 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.How You'll Create ImpactIndividual will be helping with different supplier functionalities and need to be able to project manage.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.Maintain critical gauges, procedures, and materials needed to maintain existing products.Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.What Makes You Stand OutAbility 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 SuiteProficient 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.Your BackgroundEnglish proficiendy is required (C1).B.S. in Engineering.Minimum 1 year of relevant work experience.Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferredTravel ExpectationsUp to 5% EOE/M/F/Vet/Disability
