Quality Engineering Technician

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

What You Can Expect

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. Actively supports and participates in special projects. 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

• Responsible for actively participating in investigations: Non Conformance Report (NCR), Out of Tolerance, and Customer Complaints.
• Publish Metric Trending Plans. Assist with Corrective and Preventive Action (CAPA) resolution.
• Assists 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 Engineer, may participate in department and cross functional meetings as necessary.
• Executes validation protocols, gage repeatability and reproducibility (R&R) testing, data analysis and completes the required reports.
• Coordinate the collection of test samples and ensure associated data are accurately entered, maintained, reviewed, and trended to support quality and performance monitoring.

What Makes You Stand Out

• Proficient technical writing abilities.
• Broad knowledge of good documentation practices and good manufacturing processes.  
• Ability to read and interpret blue prints and drawings.      
• Knowledgeable in the area of Geometric, Dimensioning & Tolerancing (GD&T).  
• Excellent communication, organization and problem solving skills.
• Able to work with minimum supervision and under pressure.
• Takes initiative and makes good judgment in the performance of duties.
• Computer literate: Microsoft Word, Excel and Power Point.  
  Knowledge in FDA & ISO regulations are a plus.  

Your Background

• High school diploma or GED is required.  
• Five years of relevant experience required. 
• ASQ Quality Technician Certification is highly desirable. 

Travel Expectations

• Less than 5%

Expected Compensation - $50,000- $65,000 base salary

EOE