Jobs at Vantedge Medical

Leads manufacturing process development and continuous improvement for large-format steel products and medical device components. Responsibilities include lean process implementation, root cause analysis, tooling and fixture development, CAPA management, validation, documentation, manufacturability reviews, quoting, project execution, and new product launches. The role requires cross-functional collaboration with customers, suppliers, machinists, programmers, and internal development teams while improving quality, delivery, cost, safety, and morale.

Owns engineering estimating for precision metal manufacturing opportunities. Reviews quote packages, assesses manufacturability and site fit, develops cost and pricing recommendations, evaluates processes, equipment, tooling, automation, and outside services, and identifies DFM improvements. Partners with engineering, operations, commercial, supply chain, suppliers, and customers to deliver accurate proposals. Requires technical manufacturing expertise, strong communication, GD&T knowledge, Excel proficiency, and familiarity with ISO and FDA requirements.

Leads new product introduction programs from quoting through production transition, coordinating engineering, quality, operations, supply chain, safety, suppliers, and customers. Manages schedules, budgets, risks, resources, launch criteria, manufacturing readiness, first articles, process documentation, and production ramps. Provides hands-on manufacturing engineering support involving DFM, routings, work instructions, tooling, and process troubleshooting. Also leads site growth initiatives such as equipment installations, capacity expansions, facility improvements, capital projects, and multi-site programs.

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 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.

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.