Job Summary

Zimmer Biomet is a world leader in musculoskeletal health solutions. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world. Responsible for all aspects of incoming, in-process and final inspection and related processes. With direction from Quality Management, ensures that daily inspection priorities and other assigned duties are processed. Interacts with different functional areas and suppliers to achieve established objectives.

Principal Duties and Responsibilities

• Process daily In-coming, In-process and Final inspections • Follow written procedures and blueprints utilized to complete assigned tasks • Review and assure accuracy of COAs and COCs • Administrate equipment calibration system and coordinate calibration schedules • Process Product Holds • Complete and maintain all inspection paperwork in accordance with established procedures and Good Manufacturing Practices (GMPs) • Perform final DHR review and product release for distribution • Interact with personnel from departments outside of the Quality Inspection department, including Manufacturing, Inventory Control, Engineering, etc., as required • Process Non-Conformance Reports for materials, sub-assemblies and finished product found out of specification Perform data entry tasks and procedure changes as requested by QA Management.

Expected Areas of Competence

• Ability to use simple hand-held measuring devices, including micrometers and calipers • Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding of QSR and ISO requirements • Ability to read standard operating procedures • Working knowledge of sampling techniques (e.g., ANSI Z1.4.), Good Manufacturing Practices and other regulatory standards • Ability to work within a team environment and build relationships outside of the department • Ability to communicate both orally and in written form to multiple levels of the company • Basic knowledge of Microsoft Office Suite and ability to learn QMS Software (EtQ) and ERP system (JDE)

Education/Experience Requirements

• High school Diploma or GED required plus three to five years of experience as a Quality Inspector or as a manufacturing Operator or Assembler, or an equivalent combination of education and experience. • Experience working in an inspection department for a GMP, or other regulated industry • Combination of education and experience may be considered (in evaluating experience relative to requirements)

Travel Requirements

Additional Information

EOE M/F/Vet/Disability At Zimmer Biomet, we believe in The Power of Us, which means that we are stronger together. We are committed to creating an environment where every team member feels included, respected, empowered, and celebrated.