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 Expect

　　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.

　　How You'll Create Impact

　　Developing and implementing processes, procedures and instruction to sustain and improve the Quality Management System.

　　Supporting Top Management in the development and implementation of quality systems strategies and objectives.

　　Identifying and solving product and process problems

　　Supporting various operational /manufacturing groups and suppliers in resolving and preventing quality issues

　　Performing quality engineering analysis and responses for corrective/preventive actions

　　Working with suppliers, manufacturing, engineering, and other functional areas to assist and verify the implementation and effectiveness of the corrective/preventive actions taken for non-conformance.

　　Conducting audits and assessments of internal processes and suppliers manufacturing sites

　　Developing validation strategies and support the successful execution of same.

　　Supporting and representing the site during external regulatory audits.

　　This is not an exhaustive list of duties or functions and may not necessarily comprise all of the essential functions

　　What Makes You Stand Out

　　Bachelor’s Degree in Quality or Engineering field, or an equivalent combination of education and experience.

　　Must be familiar with Microsoft Office Suite

　　Must have minimum of 5 years of experience in Quality Engineering field

　　Experience of working in a regulated industry, preferably medical devices.

　　Your Background

　　Must be familiar with all aspects and elements of a quality system including but not limited to management responsibility, resource management, product realization and measurement, analysis and improvement processes.

　　Knowledge on aspects of quality assurance techniques such as: inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control

　　Demonstrated technical expertise

　　Demonstrates ownership for the integrity of work

　　Able to work independently or as part of a team and consider options for completing work

　　Strong written and verbal communication skills

　　Travel Expectations

　　EOE/M/F/Vet/Disability