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.

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 ZB to achieve Zimmer Biomet Quality goals.

How You'll Create Impact

• Formulates procedures, specifications, and standards for Zimmer products and processes.

• Develops and implements corrective/preventive action plans.

• Collects and analyzes data for gauge and product evaluation.

• Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.

• Ensures that suppliers have the required information and facilities to deliver quality products to Zimmer.

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.).

• High attention to detail in analytics, presentations, and communication; including logical structuring.

• Able to communicate in both oral and written form to multiple levels of the company.

• Ability to deliver, meet deadlines, and have results orientation.

• Excellent Microsoft Office skills (PowerPoint, Word, and Excel)

• Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods.

• Ability to define project goals and objectives, and track and report progress against defined goals to project stakeholders across multiple functional groups (internal and external, such as suppliers).

• Demonstrates characteristics of high potential for future development opportunities.

Your Background

• English proficiency is required (C1)

• B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE).

• 0-3 years of work experience.

• Combination of education and experience may be considered (in evaluating experience relative to requirements)

• Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred

• Experience in medical device regulations is a plus.

Please note that you must submit your resume in English at the time of applying, or your application will not be considered.

Travel Expectations

Up to 20%

EOE/M/F/Vet/Disability