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 talented 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 inspired, invested, cared for, valued, and have a strong sense of belonging.

Duties

The Quality Senior Engineer I will 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. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Ensure products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interact with many different functional departments, suppliers, and experts outside Zimmer to implement Zimmer Quality goals.

 

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; ensure that suppliers have necessary information and facilities to deliver quality products to Zimmer.

Requirements - Education and Experience

Education

Requires a bachelor’s degree in biomedical engineering or related engineering field. Must have 3 years of experience in the job offered or a related position.

Experience

Must have 3 years of experience with the following: Risk Management File; Microsoft Office Suite; Blueprint reading and geometric dimensioning and tolerancing; QSR/ISO regulations, design assurance, FMEA, and product testing methods; Optical comparators and CMMs; Design controls, risk management, and verification and validation tools and methodologies.

Must have 2 years of experience with knowledge of statistics, process control, and process capability.

Travel Expectations

Up to 20% of domestic travel required.

LOCATION:  Biomet Manufacturing, LLC (formerly Corp.), 1800 West Center Street, Warsaw, IN 46580

EOE/M/F/Vet/Disability