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As a Manufacturing Engineer, you will support the development, validation, and scale-up of manufacturing processes for our innovative surgical device - directly contributing to product quality, efficiency, and patient outcomes. In all actions, the Manufacturing Engineer will demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented processes and procedures\nManage special projects and initiatives as assigned, driving them from planning through implementation and final completion\nLead development and optimization of manufacturing processes for soft-tissue repair device systems\nDrive design for manufacturability (DFM) and transfer of robust processes into high-volume production\nDevelop and validate equipment, fixtures, and tooling for assembly and inspection\nPartner cross-functionally with R&D, Quality, and Supply Chain to resolve technical issues and improve output\nExecute structured root-cause analysis and corrective actions for production challenges\nSupport process validations, change controls, and documentation in compliance with ISO 13485/FDA QSR\nSkills:\n7-10+ years engineering experience in manufacturing or 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