Process Engineer

Who We Are ABOUT ENOVIS™ Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com. What You'll Do At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it. Because that’s how we change the lives of patients for the better. And that’s how we create better together. Why work at Enovis? See for yourself. As a key member of the Manufacturing Team you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes. Job Title: Process Engineer, New Product Introduction Reports To: Manager, Process Engineering Location: Austin, Texas Business Unit Description: Enovis Surgical Job Title/High-Level Position Summary: As a Process Engineer NPI (New Product Introduction) you will be responsible for the design and development of new and/or improved manufacturing processes and ensuring efficient and effective design transfer of product into production. Be part of the cross functional team to lead/manage all aspects of process development to implement manufacturing processes both within Enovis and at its suppliers. Drive improving existing manufacturing processes within the New Product Development project, which then may be shared across other production lines. Key Responsibilities: Serves as a cross functional team member as primary process and manufacturing expert on new product introduction cross functional teams. Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on new development projects. Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation. Executes the functional deliverables associated with the CAPA, Project Management, and Quality Systems. Plans, organizes, and conducts all aspects of manufacturing technical reviews. Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM’s, Routers, FMEA’s, etc.) Writes and reviews validation protocols and reports applicable to new processes. Oversees development builds associated with the project using technical work requests. Provides Design for Manufacturability (DFM) input to the engineering print package. Responsible for conveying the process and manufacturing limits and capabilities to the development team. Contributes ideas to or generates Intellectual Property submissions. May train manufacturing personnel when required as part of a validation. Participate in lean reviews, and Kaizen events. May coach technicians or other engineering support employees. Minimum Basic Qualifications: This position requires bachelor’s degree in science or BSME, or related Engineering Minimum of 7 years of experience in process/manufacturing engineering role. Level may be based on years of experience. Travel Requirements: