Phillips Precision Medicraft is hiring: Manufacturing Engineer in Elmwood Park

Phillips Precision Medicraft (PPM) is a trusted, single-source provider of advanced orthopedic manufacturing solutions , specializing in implants, instrumentation, and sterilization delivery systems. For over 52 years, PPM has been manufacturing from three U.S.-based, ISO13485-certified, and FDA-registered facilities, ensuring the highest quality standards. By emphasizing continuous improvement and value stream partnerships, PPM delivers innovative solutions, effective inventory management, and design for manufacturability (DFM) services. Committed to quality and seamless client relationships, PPM strives to provide exceptional responsiveness and expertise for ongoing success in the orthopedic industry. Role Description We are seeking a detail-oriented and collaborative Manufacturing Engineer to support both New Product Introduction (NPI) and existing product lines. This role will serve as a critical link between engineering, operations, and customers to ensure manufacturing processes are efficient, cost-effective, and aligned with quality standards. The ideal candidate will be proactive in driving continuous improvement, maintaining documentation, and fostering strong cross‑functional relationships. This position requires a strong focus on Design for Manufacturability (DFM), acting as a key liaison between customers and internal teams to ensure that product designs are optimized for production capabilities and cost efficiency. Qualifications Bachelor’s degree in Manufacturing Engineering, Mechanical Engineering, or a related field. 3+ years of experience in a manufacturing or industrial engineering role. Strong understanding of DFM principles, control plans, and ECN processes. Experience with ERP/MRP systems (VMFG experience preferred). Excellent communication and interpersonal skills, with the ability to interface effectively with customers and cross-functional teams. Proficiency in CAD software and Microsoft Office Suite. Demonstrated ability to lead cross-functional teams and drive process improvements. Familiarity with CNC machining and quality assurance processes is a plus. Key Responsibilities Collaborate with customers during design and development phases to review part designs and provide DFM feedback that enhances manufacturability, reduces cost, and improves production efficiency. Lead DFM review sessions with customers and internal stakeholders to identify and address potential design or process issues early in the development cycle. Act as the primary liaison between customers and internal departments (Engineering, Quality, Operations, CNC Applications), ensuring clear communication and timely resolution of technical issues. Coordinate internal engineering activities to align with customer requirements, project timelines, and production readiness. Manage Engineering Change Notices (ECNs) through VMFG and ensure timely updates to control plans, digital attachments, and related documentation. Communicate with customers regarding prints, specifications, and process clarifications to ensure alignment and manufacturability. Oversee project and part timelines, track current work status, estimate completion dates, and provide regular updates to senior management on project status, risks, and performance metrics. Partner with the Quality Department to address nonconforming products and update control plans as needed. Research and recommend new manufacturing technologies and process improvements to enhance productivity, product quality, and operational efficiency. Drive continuous improvement initiatives focused on reducing cycle time, setup time, and production costs, while improving work holding and lead times for first‑article inspections. Ensure smooth handoff between Engineering and Operations, confirming parts are production-ready and running correctly. Maintain a clean, organized, and professional work environment, and lead by example in adhering to all company policies and procedures. Preferred Skills Lean Manufacturing or Six Sigma certification. Experience in a high‑mix, low‑volume manufacturing environment. Knowledge of ISO 9001 or other quality management systems. Experience in Implants and Instrumentation Orthopedic Manufacturing. Physical Demands Required to stand for long periods of time. May involve some repetitive motions. Must be able to lift up to 25 pounds. May also engage in frequent bending, stooping, squatting, pushing and pulling. Seniority level Not Applicable Employment type Full-time Job function Engineering and Production Manufacturing and Medical Equipment Manufacturing #J-18808-Ljbffr