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 primary responsibility of this position is to assure conformance to established regulatory requirements and standards through effective implementation of Quality Management System principles and processes. Further responsibilities entail/include managing projects on a corporate/global level, focusing on compliance and continuous improvement with cross-functional departments, sites, suppliers and experts within and outside Zimmer. This position also entails/includes directing and/or supporting the Quality Management Processes including but not limited to Supplier Quality Management, Supplier Audits, Corrective and Preventive Action and Validation in order to communicate and implement Zimmer Quality Objectives. 

•        Managing corporate supplier quality systems projects for the development and implementation of processes, procedures and instruction to sustain and improve the Supplier Quality Management System. 

•        Supporting top management in the strategic planning of quality systems strategies and objectives.

•        Managing cross-functional and cross-divisional teams in the development and implementation of corporate quality systems strategies and objectives.

•        Managing corporate quality systems initiatives for the development & implementation of harmonized supplier quality systems, best practices across the organization.

•        Identifying and solving continuous improvement opportunities for the improvement and increased efficiency of Zimmer's quality systems.

•        Identifying and solving product, system and process problems.

•        Supporting various groups as needed for conducting audits and assessments of internal processes and suppliers manufacturing sites, CAPA etc.

Requirements - Education and Experience

Requires a bachelor’s degree in Engineering, Business Administration, Finance, or related field.

Must have 5 years of experience in the Quality / Regulatory Compliance field or related field.

Must have 2 years of experience in Project Management.

Must have 3 years of experience with quality assurance techniques such as:  inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control.

Must have 3 years of experience showing knowledge on aspects of quality assurance techniques such as:  inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control.

Must have 3 years of experience with Microsoft Suite.

 

Travel Expectations

Up to 15% of domestic travel required.
LOCATION: Zimmer, Inc., 1800 W Center St., Warsaw, IN 46580

EOE/M/F/Vet/Disability