• 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.

Requires a bachelor’s degree in biomedical engineering or related engineering field.

Requires 3 years of experience in the job offered or a related position.

Must have 3 years of experience with:

• 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; and
• Design controls, risk management, and verification and validation tools and

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

Position requires up to 20% domestic travel.