Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!

What You Can Expect

Gather relevant, factual information and data in order to solve quality related problems; resolve issues by identifying and applying solutions from acquired technical experience and guided precedents; formulate procedures, specifications, and standards for Zimmer products and processes; provide leadership for quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance; develop and implement corrective/preventative action plans; collect and analyze data for gauge and product evaluation; identify critical personnel, gauges, procedures, and materials needed for the completion of new products; and ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer.

How You'll Create Impact

What Makes You Stand Out

Must have 3 years of experience in job offered or related position and must have 3 years of experience with the following: FDA regulated industry experience with extensive knowledge of FDA 21 CFR Part 820, Part 803 and Part 806, ISO13485, and ISO17971; Microsoft Office Suite, Blueprint reading and geometric dimensioning and tolerancing; and QSR/ISO regulations, design assurance, FMEA, and product testing methods. Must have 2 years of experience with the following: Training experience to a technical audience; and problem solving through use of quality and statistical tools.

Your Background

Requires a bachelor's degree in Mechanical Engineering or related Engineering field, or foreign equivalent.

Travel Expectations

Position requires up to 20% of domestic travel. 40 hours per week, Monday through Friday, 8:30 AM to 5:00 PM Zimmer Biomet CMF and Thoracic, LLC, 1520 Tradeport Drive, Jacksonville, FL 32218

EOE/M/F/Vet/Disability