Quality Engineering Technician

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

The Quality Engineering Technician works with the Quality Engineers supporting: day to day operations, Non Conformance Reports-(NCRs), Out of Tolerance Gage Reports, Customer Complaints, Corrective and Preventive Action- (CAPA) development and implementation, Operational Procedures revisions and Continuous Improvement (CI) initiatives.

He/she actively supports and participates in special projects, and performs all duties with strict observance of company's procedures, GMP's, SOP's and other internal and external requirements or regulations.

How You'll Create Impact

• In a timely manner, identify, report and seek corrections for calibration out of tolerance (OOT) incidents.

• Responsible for actively participating in investigations: Non Conformance Report (NCR), Out of Tolerance, and Customer Complaints.

• Publish Metric Trending Plans for Calibration. Assist with Corrective and Preventive Action (CAPA) resolution.

• Assist with revising Operational Procedures and Continuous Improvement (CI) initiatives.

• Training delivery to other team members that will perform tasks related to the same area.

• In the absence of the QA Calibration Engineer, may participate in department and cross functional meetings as necessary.

• Execute validation protocols, gage repetitivity and reproducibility (R&R) testing, data analysis and completes the required reports.

• Complete Vertex, CMM programming and SPC template completion.

What Makes You Stand Out

• The ideal candidate has strong technical writing skills and broad knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

• Ability to read and interpret blueprints and technical drawings and possess knowledge of Geometric Dimensioning and Tolerancing (GD&T).

• Demonstrates excellent communication, organizational, and problem-solving skills, can work effectively with minimal supervision and under pressure, and shows initiative and sound judgment in the performance of duties.

• Proficiency in Microsoft Word, Excel, and PowerPoint.

• Knowledge of FDA and ISO regulations preferred.

Your Background

• Minimum Requirements: High School Diploma or Equivalent and 2 years of relevant experience

• ASQ Quality Technician Certification is highly desirable.

Travel Expectations

Less than 5%.

EOE