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 recognized.
What You Can Expect
You will work with the quality engineers supporting: day to day operations, Non Conformance Reports-(NCRs), Out of Tolerance Gage Reports, Customer Complaints, Corrective and Preventive Action- (CAPA) development and implementation, Operational Procedures revisions and Continuous Improvement (CI) initiatives. In addition to this you will actively support and participate in special projects.
All duties will be performed with strict observance of company’s procedures, GMP’s, SOP’s and other internal and external requirements or regulations.
Execute incoming inspection activities on finished goods and components received from suppliers.Responsible for actively participating in investigations: Non Conformance Report (NCR), Out of Tolerance, and Customer Complaints.Assist with Corrective and Preventive Action (CAPA) resolution.Assists with revising Operational Procedures and Continuous Improvement (CI) initiatives. Training other team members that will perform tasks related to the same area.In the absence of the Quality Engineer, may participate in department and cross functional meetings as necessary. Assist in achieving other regulatory objectives (e.g., QSR training, Quality Program applications) at the direction of the manager.
What Makes You Stand Out
Ability to work towards a thorough knowledge of Zimmer-Biomet’s processes and products. Broad knowledge of good documentation practices and good manufacturing processes. Good communication, organization and problem solving skills. Must be reliable and capable of working with minimal supervisionMust be able to manage sensitive issues; firmly adhering to the principles of the regulations, guidelines and procedural requirementsComputer literate: Microsoft Word, Excel and Power Point. Knowledge in FDA & ISO regulations are a plus. Your Background
High school diploma or GED is required. Five years of manufacturing/quality experience required. ASQ Quality Technician Certification, or equivalent, is highly desirable.
EOE/M/F/Vet/Disability