Jobs at LSI Solutions

Programs, sets up, operates, and troubleshoots Swiss-style and Mill Turn CNC machines to produce precision medical-device components. Responsibilities include reading prints and CAD models, inspecting parts, applying GD&T, adjusting tool paths, resolving process issues, writing macros, supporting prototyping, training machinists, and meeting productivity and quality KPIs in an overnight manufacturing environment.

Develops, improves, validates, and supports manufacturing processes and equipment for regulated medical devices. Responsibilities include process control plans, equipment specification and implementation, troubleshooting, root cause analysis, corrective actions, continuous improvement, risk analysis, measurement systems analysis, validation, documentation, tooling support, and production technician guidance. The role works onsite in a cleanroom for approximately 80% of the shift and ensures compliance with safety, quality, and regulatory requirements.

Programs, sets up, operates, and troubleshoots Swiss-style and Mill Turn CNC machines to produce precision medical device components. Reads blueprints, CAD models, process documentation, and GD&T requirements; performs inspections and adjustments; develops complex multi-axis programs and macros; resolves process issues; supports prototyping, training, productivity, quality, and continuous improvement initiatives.

Manages cross-functional engineering projects supporting medical device product development, design enhancements, and manufacturing improvements. Responsibilities include planning, scheduling, coordinating technical work, controlling scope, budgets, timelines, and deliverables, communicating project status, leading review meetings, maintaining regulatory-compliant records, resolving technical issues, and guiding project teams. Senior levels also manage complex programs, mentor project managers, and coordinate resources across functional leaders.

Provides quality engineering support for regulatory compliance, QMS development, documentation, gap assessments, CAPA investigations, audits, metrics, and continuous improvement. The role develops procedures and quality plans, tracks projects, supports inspections, performs root cause analysis, and may mentor engineers and lead CAPA activities. Candidates should have strong analytical, communication, training, and problem-solving skills, plus familiarity with SPC, CpK, DOE, FMEA, and Lean tools.

Fabricates precision components, prototypes, production parts, tools, and fixtures using manual and CNC machine tools. Collaborates with engineers and designers on drawings, tolerancing, design for manufacturing, and process improvements. Senior Toolmakers develop fabrication processes, program machines, perform tolerance analysis, research equipment and software, and delegate work. The role requires independent project leadership, mentoring junior staff, and working with metals and plastics.

Design and improve minimally invasive surgical instruments and components, owning form, fit, function, and feel. Lead complex designs, design reviews, FMEA, tolerance stack-ups, failure analysis, manufacturability improvements, CAD documentation, testing, and validation support. Collaborate with Product Engineering, Manufacturing, and Operations, while providing technical leadership and mentorship on major projects. Apply FEA, GD&T, robust design, DOE, statistical analysis, and FDA/ISO standards to develop safe, reliable medical devices.

Configure and maintain product data in the EIQ ERP system, including BOMs, item masters, device master records, engineering BOMs, and work orders. Track engineering changes, reworks, deviations, and work orders while ensuring data accuracy and resolving discrepancies. Configuration Analyst II responsibilities additionally include maintaining workflows, supporting ERP enhancement projects, coordinating configuration information, and training staff. The role collaborates with Engineering, Planning, Production, customers, and ERP Systems teams.

Analyze production performance, manufacturing operations, equipment utilization, work orders, cycle times, and engineering bills of materials. Maintain Crystal Reports and Tableau dashboards, produce executive and sales reporting, document business requirements, support IQMS pricing and cost data, identify data integrity issues, and recommend process improvements. The role also assists with contract negotiations and collaborates with production teams and subject matter experts.

Manages cross-functional engineering projects involving new product and systems development, design enhancements, and manufacturing improvements. Establishes scope, schedules, budgets, deliverables, and project records; leads project meetings and phase-gate reviews; communicates status and resolves technical obstacles. Senior levels independently manage complex programs, coordinate functional leaders, escalate issues, develop project-management tools, and mentor project personnel. Work must comply with medical-device quality and regulatory standards.

Program, set up, and operate Swiss-style and Mill Turn CNC machines to produce precision medical-device components. Read drawings and CAD models, apply GD&T, inspect parts with precision instruments, troubleshoot tool paths and processes, perform preventive maintenance, and support production reporting, training, prototyping, and continuous improvement.