Engineer II, NPI & Transfers

Responsible for supporting medical devices for both existing and new product development, production, and processes. This includes creating or verifying specifications, maintaining, and enhancing product processes, and designing fixtures and equipment, testing processes, equipment, test methods, and raw materials to ensure that the concepts and prototypes meet their specifications.

Support projects related to new product introductions, process development engineering, quality systems improvement, and other engineering tasks. Evaluate, initiate, and establish improved engineering and process validation. Support new and existing manufacturing processes, new products, product changes and enhancements, as well as related tooling and fixtures 2. Draft and execute validation of product, equipment, and processes 3. Provide mechanical design concepts for new equipment and fixturing to improve manufacturing process capability, capacity, efficiency, cost, and quality 4. Lead builds for new product development in prototype and pilot production settings, including training of operators and coordination with production planning 5. Analyze data and improve processes to assure robust/repeatable manufacturing processes 6. Confer with appropriate departments, resources, and/or outside services to prepare process modifications, clarify problems, and develop processes 7. Support projects related to process validation and product transfer activities across different manufacturing facilities and product lines 8. Develop manufacturing documents (e.g., MP, Routers, BOM, Drawings, Specifications, etc.) 9. Develop and maintain project timelines, milestones, and deliverables to ensure smooth execution of the NPI process 10. Collaborate with the quality team to establish testing and inspection protocols to ensure the final product meets quality standards 11. Collaborate with design engineers to optimize product designs for efficient manufacturing and assembly processes 12. Review product designs to identify potential manufacturability and assembly issues, providing recommendations for improvements 13. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization 14. Perform additional duties as assigned