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. **Duties - Senior Quality Engineer I** The Senior Quality Engineer I will gather relevant, factual information and data in order to solve quality related problems; resolve issues by identifying and applying solutions from acquired technical experience and guided precedents; plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines; ensure 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 to implement Zimmer Quality goals; formulate procedures, specifications, and standards for Zimmer products and processes; lead quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance; develop and implement corrective/preventative action plans; collect and analyze data for gauge and product evaluation; identify critical personnel, gauges, procedures, and materials needed for the completion of new products; and ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer. **Requirements - Education & Experience** **Education** - Requires a Bachelor's degree in Engineering or related field, or foreign equivalent. **Experience** - Must have 3 years of experience in a Quality Engineering role. Must have 3 years of experience with the following: • Microsoft Office Suite; • knowledge of blueprint reading and geometric dimensioning and tolerancing; understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods; and • using optical comparators and CMMs. Must have 1 year of experience with medical device regulations. **Travel Expectations** Up to 20% of domestic travel required. Telecommuting work arrangement permitted: position may work in various unanticipated locations throughout the U.S. Remote work permitted up to 5 days per week throughout the U.S. EOE/M/F/Vet/Disability