The Technical Service Coordinator serves as a liaison among Customer Service Representatives, Sales, Quality, Operations, and Engineering to support medical sterile packaging products and converting operations. The role coordinates technical activities across the product lifecycle, including new product introduction, customer specification changes, validation support, complaint investigations, and continuous improvement initiatives. It ensures customer requirements are accurately translated into manufacturing specifications while maintaining compliance with applicable standards, quality systems, and customer-specific requirements. Strong attention to detail, accuracy, and the ability to perform repetitive tasks with minimal errors are important. A strong understanding of purchase orders and forecasting is required. The coordinator is the primary technical contact for assigned customers, interpreting drawings, specifications, and quality requirements; responding to technical inquiries; supporting audits and technical reviews; and coordinating resolution of concerns and technical issues. The role also supports customer service, scheduling, and purchasing teams to ensure orders and jobs are entered accurately and on time, providing backup for scheduling and purchasing as needed. The position works with Operations and Engineering to keep order specifications and product revisions aligned with approved product documentation. It processes new product requests and engineering changes; coordinates product documentation in IQMS, including specifications, drawings, bills of material, routing instructions, and work instructions; supports new materials, equipment, and processes; and coordinates validation activities and engineering work orders. It tracks and trends customer response time, specification updates, product quality, and production performance, and supports continuous improvement. The coordinator ensures documentation is complete, accurate, and audit-ready; maintains knowledge of applicable ISO standards and validation requirements; supports compliance with ISO 13485, ISO 11607, FDA Quality System requirements, and GMP practices; and assists with nonconformance investigations and CAPA activities. The role maintains technical knowledge of Tyvek materials, medical-grade papers, PE and co-extruded films, header bags, pouches, rollstock, and heat-sealing technologies. The employee must understand and comply with SPG and DuPont safety policies and procedures, recognize and report hazards, and promptly report work-related pain or injury. The position requires remaining stationary for approximately 75% of the workday and occasionally lifting up to 20 pounds.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree