Zimmer Biomet

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; assure products conform to established requirements and standards through appropriate audit, inspection, and test activities; formulate procedures, specifications, and standards for Zimmer products and processes; lead 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 3 years of experience in the FDA regulated industry including with processes and procedures to maintain company compliant.

Must have 3 years of experience with 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:

• Six Sigma project experience;
• training experience to a technical audience; and
• problem solving through use of quality and statistical tools.

Your Background

• Requires a Bachelor’s in Mechanical Engineering or related engineering field or foreign equivalent.

Travel Expectations

• Role requires 20% of domestic travel.
• 40 hours per week, Monday through Friday, 8:30 AM to 5:00 PM

Zimmer, Inc., 1800 West Center Street, Warsaw, IN 46580

EOE/M/F/Vet/Disability