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Supports manufacturing engineers and operations through time studies, process improvement, facility layout updates, work instruction and manufacturing document revisions, non-conformance investigations, shop-floor problem solving, and data entry. The intern works under regular supervision and contributes recommendations for minor process improvements. The role requires pursuing a mechanical or manufacturing engineering degree and familiarity with CAD, SolidWorks, metal fabrication, and Microsoft Office.

Leads Manufacturing Engineering and New Product Introduction activities, manages engineering personnel, directs technical projects, and oversees manufacturing process improvement. Responsibilities include workload planning, engineering procedures, quality and safety initiatives, documentation, hardware and software implementation, performance management, and cross-functional stakeholder communication. The role requires extensive manufacturing experience, medical device exposure, ERP/MRP knowledge, CAD/CAM familiarity, and expertise in FMEA, APQP, GD&T, and sophisticated quality systems.

Leads manufacturing process development and improvement for medical device and data center contract manufacturing. Responsibilities include lean process implementation, root cause analysis, CAPA management, new product launches, tooling and fixture development, engineering documentation, validation protocols, design-for-manufacturability reviews, and process technology development. The role collaborates with cross-functional teams, customers, suppliers, machinists, and programmers to improve quality, delivery, cost, safety, and productivity.

Leads supply chain activities for new product introductions, product transfers, and manufacturing launches. Manages sourcing, purchasing, supplier performance, production planning, material readiness, inventory, and supply chain risk. Partners cross-functionally with engineering, manufacturing, quality, program management, commercial teams, customers, and suppliers. Supports quoting, cost estimation, ERP/MRP planning, reporting, KPI tracking, continuous improvement, and production ramp activities.

Leads manufacturing process development and continuous improvement for precision medical-device components. Responsibilities include PECM and ECF process development, validation, tooling and fixture design, new product introductions, process transfers, root cause analysis, CAPA management, documentation, customer communication, and cross-functional project leadership. The role also supports Lean Manufacturing, quality-system compliance, emerging technology evaluation, and operational improvements in quality, cost, delivery, and capacity.

Supports production through CNC setup, troubleshooting, operator training, process improvement, equipment qualification, and manufacturing documentation. Collaborates with customers on design for manufacturing, resolves production issues, and supports new product introduction. Responsibilities include quoting technical input, creating drawings, tooling layouts, CNC programs, routing steps, performance monitoring, and training. The role requires substantial machining experience and knowledge of Swiss, vertical milling, and 5-axis CNC processes.

Owns general ledger accounting and month-end close for a manufacturing facility, including labor journal entries, accruals, reconciliations, cash book management, and audit support. Provides FP&A variance analysis and reporting assistance while supporting standard costing, inventory valuation, manufacturing variance analysis, and inventory counts. The role also strengthens close processes and internal controls while working onsite with operations and plant personnel.

Leads a team of automation engineers and technicians, providing hands-on expertise in robotics, PLCs, machine vision, fixturing, and material handling. Owns automation capital planning, ROI analysis, vendor and integrator relationships, process assessments, and automation solution development across manufacturing sites. Partners with Finance, Operations, Commercial, and site leadership to prioritize investments, improve safety, productivity, and quality, and validate automated processes in regulated manufacturing environments.