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Support and improve existing processes using Statistical, Lean, Good Manufacturing Practice (GMP) and Six Sigma methodologies. Effectively transfer new products, design changes or line extended devices on to production floor. Foster an environment of continuous improvement and provide support to customers in all functional areas. Discuss progress and interim findings at periodic design/project review meetings. Perform Failure Analyses (FAs) and improve Functionality/Performance of medical devices. Identify and implement process improvements and machining improvements on production lines. Reduce Reject Rates(scrap) and optimize manufacturing processes. Identify and implement safety improvements on production lines. Lead the development and execution of technical protocols and, generation of reports. Develop and implement operating procedures, standard work, visual work instructions, visual work references. Provide training to Production for all new product launches and design changes to existing products or processes. Expectation of acquired knowledge of FDA/ISO requirements associated with the development of medical devices including Design Control. Perform other duties as directed or assigned by Manager.