At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.  

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

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