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; resolve issues by identifying and applying solutions from acquired technical experience and guided precedents; evaluate process methods and equipment to meet performance and quality requirements; establish quality plans for equipment and processes for general and specific product performance needs; monitor performance of processes to a standards; apply ISO and QSR requirements to processes and procedures for Zimmer and outside suppliers; work with suppliers on new product introduction to insure that quality and performance requirements are fulfilled; assist Manufacturing, Sourcing and Development in the interpretation and application of regulations; develop and maintain department and project budgets.

How You'll Create Impact

What Makes You Stand Out

Must have 3 years of experience in job offered or related position.

Must have 6 months of experience with the following:

• Working with third party suppliers related to nonconformance investigation and continuous improvement;
• Working in manufacturing processes environment;
• Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs;
• Evaluating nonconformance root cause, implementing corrections and containment; and Statistics, process control, and process capability.

Your Background

Requires a Bachelor’s in Biomedical engineering, Mechanical engineering, or related engineering field, or foreign equivalent.

In lieu of a bachelor’s and 3 years of experience, the company will accept the following: Requires a Master’s degree in Biomedical engineering, Mechanical engineering, or related engineering field, or foreign equivalent. Must have 1 year of experience in job offered or related position. Must have 6 months of experience with the following: Working with third party suppliers related to nonconformance investigation and continuous improvement; Working in manufacturing processes environment; Microsoft Office Suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, understanding of QSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use optical comparators and CMMs; Evaluating nonconformance root cause, implementing corrections and containment; and Statistics, process control, and process capability.

Travel Expectations

• Position requires up to 20% of domestic travel. Position permits remote work up to 5 days per week.

CD Diagnostics Inc., 56 E Bell Drive, Warsaw, IN 46582

EOE/M/F/Vet/Disability