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Job Summary

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.

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.

Principal Duties and Responsibilities

• 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.
• 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 Calibration Engineer, may participate in department and cross functional meetings as necessary. Executes validation protocols, gage repetitivity and reproducibility (R&R) testing, data analysis and completes the required reports.
• Completes Vertex, CMM programming and SPC template completion.

Expected Areas of Competence

• 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.

Education/Experience Requirements

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

Travel Requirements

• Minimal

Additional Information

Zimmer Biomet is a world leader in musculoskeletal health solutions. 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.

EOE M/W/Vet/Disability This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA.

At Zimmer Biomet, we believe in The Power of Us, which means that we are stronger together. We are committed to creating an environment where every team member feels included, respected, empowered, and celebrated.