Vacancy expired!
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 Managing manufacturing engineering services such as cell management, process development, project management, and process validation, to support end of line manufacturing processesspecific to cleaning and packaging; Plan and review work assignments for staff and coaching and developing staff; Develop and improve end of line processes (cleaning, upgrade, & packaging) using process validation and continuous improvement methodology; Solve a variety of complex process and product performance issues; Develop and implement plan to set new process performance and quality standards: scrap percentage, perishable costs, lead time reductions, and customer service issues; Pursue and monitor corrective and preventive actions for applicable processes; Develop and maintain engineering budgets for capital projects and manufacturing costs; Conduct manufacturing, development, and quality process/procedures; Assist department efforts in audits, both internal and external, to demonstrate compliance with GMP, ISO, and MDD regulations; and Monitor manufacture performance using quality and statistical tools.Responsibilities - Education and ExperienceRequires a Bachelor’s degree in Engineering Management, Engineering, Computer Science, or related field, or foreign equivalent.Must have 5 years of experience in the job offered or related position.Requires experience with all of the following:
Quality System Regulation and Associated regulations and standards;
PLM (Product Life Cycle Management) & ERP;
Control procedures, including Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions.
Travel Expectations100% on site - Up to 10% domestic travel required.LOCATION : Zimmer, Inc., 1800 W. Center Street, Warsaw, IN 46580EOE/M/F/Vet/Disability
Vacancy expired!