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Sr. Manufacturing Engineer - Packaging

Job Description
Requisition ID:
38382
Title:
Sr. Manufacturing Engineer - Packaging
Division:
Arthrex Manufacturing Inc
Location:
AMI East- AMI- Ave Maria, FL
Main Objective:
Design, develop, and implement automated device assembly, packaging, and labeling processes to produce cost effective quality medical device products and systems. Provide manufacturing engineering expertise to create, document and implement required procedures and documents.
Essential Duties and Responsibilities:
Drive automation to replace manual inspection, assembly, and packaging/labeling processes.
Work with project teams to identify issues and risks and propose corrective actions.
During new product development, represent the Packaging Production Department to ensure cost effective new product development and introduction into production assuring Design for Manufacturing (DFM).
Develop a continuous improvement culture, skills sets and tools to enhance quality and operational excellence.
Lead/support process improvement initiatives, identifying best practices.
Introduce new fixtures, equipment, and processes. Present process and equipment recommendations to Leadership Team with plans for implementation. Manage automation equipment related capital projects with outside suppliers to meet project scope, cost, and schedule.
Develop an understanding of the current final device assembly and packaging processes and identify targets for improvement in operation efficiencies.
Develop manufacturing Work Instructions, Inspection Plans, and Statistical Process Controls.
Provide process and equipment expertise and support for daily clean-room production and sterile packaging efforts.
Develop action plans to achieve short and long-range efficiency goals, selection of new production methods, designs of production fixtures, and methods to monitor efficiencies.
Lead and/or assist with implementation of packaging design/and or production specifications into manufacturing.
Monitor timelines and project deliverables to ensure adherence with approved project plans for production process development.
Develop protocols and coordinate validation of equipment and processes.
Stay current with methods used in the medical device industry to advance technologies.
Participate in defining Preventive Maintenance programs for clean room equipment/ and or production equipment.
Ensure Information and documentation is consistently accurate.
Analyze and plan workforce utilization, space requirements, and Lean workflow, layout of equipment and workspace for maximum efficiency.
Confer with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards.
Estimate production times, staffing requirements, and related costs to provide information for management decisions.



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