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Leads an R&D engineering team developing advanced manufacturing processes and technologies for precision medical devices. Manages personnel, resources, project execution, customer communications, technical innovation, laboratory operations, budgets, and cross-functional collaboration. Oversees complex development programs from feasibility through implementation, including process development, automation, inspection, equipment, risk management, quotations, and transition into production.

Leads multi-site, cross-functional technical and operations programs from planning through completion. Manages scope, schedules, budgets, resources, risks, stakeholder communications, and issue resolution. Coordinates design transfers, manufacturing launches, and line transfers across sites, ensuring compliance, quality, and successful handoff to operations. Presents to executives and influences teams in matrixed environments. Requires extensive technical program management experience, with medical products, contract manufacturing, ISO 13485, and PMP experience preferred.

Leads complex, multi-site technical programs supporting medical device product development, design transfer, manufacturing launches, and line transfers. Coordinates cross-functional engineering, operations, procurement, commercial, and external partner teams; manages scope, schedules, budgets, resources, risks, quality, and customer communications. Produces executive status reporting, drives issue resolution, oversees procurement, and ensures programs meet performance, cost, timing, and quality commitments.

Leads complex, multi-site technical programs from scope definition through manufacturing launch and product transfer. Coordinates cross-functional engineering, operations, procurement, commercial, and customer teams; manages budgets, schedules, risks, resources, documentation, and stakeholder communications. Oversees design transfers, manufacturing and line transfers, supplier coordination, issue resolution, process improvements, and delivery against performance, cost, quality, and timeline commitments.

Leads complex, multi-site technical programs for medical device manufacturing, including design transfers, manufacturing launches, line transfers, customer coordination, resource allocation, budgeting, scheduling, risk mitigation, procurement, and cross-functional execution. Manages matrixed teams, communicates progress to stakeholders and executives, resolves escalations, and ensures programs meet performance, cost, quality, and delivery commitments.

Leads and mentors manufacturing engineering teams supporting high-volume contract manufacturing and medical device production. Responsibilities include process and equipment development, product launches, validation, quality investigations, capital planning, safety compliance, tooling support, continuous improvement, technical documentation, customer interactions, and production cost quoting. Requires extensive supervisory and high-tech manufacturing experience, ISO expertise, and knowledge of machining, tooling, engineering standards, and analytical methods.

Manages complex production and material planning, balancing demand, capacity, inventory, materials, and delivery commitments. Leads cross-functional planning, ERP data and parameter management, inventory and purchasing analysis, KPI monitoring, recovery planning, new product transitions, and continuous improvement initiatives. Serves as the site planning and ERP subject matter expert while identifying risks and driving corrective actions in a regulated manufacturing environment.

Leads plastic injection molding process transitions, validations, improvements, and optimization through manufacturing control. Manages scientific molding validations, troubleshooting, corrective actions, documentation, customer project meetings, and cross-functional manufacturing support. Requires engineering expertise, hands-on machine operation, statistical validation analysis, Lean Six Sigma, project management, budgeting, and knowledge of mold tooling and automation. Ensures compliance with quality, safety, and regulatory requirements while supporting multiple initiatives and meeting project deadlines.

Leads end-to-end development of complex interventional medical devices, including concept generation, SolidWorks design, prototyping, testing, verification, risk management, and design controls. Serves as technical and project lead for customer programs, manages schedules and decisions, supports quality compliance and clinical studies, mentors junior engineers, and drives process improvement across multiple concurrent projects.

Leads the development, optimization, validation, and implementation of medical device manufacturing processes. Responsibilities include coordinating projects, equipment and facility planning, manufacturing launches, process and quality analysis, engineering change orders, production transfers, capital expenditure justification, automation initiatives, and lean manufacturing improvements. Provides technical leadership and coaching while collaborating cross-functionally with operations, quality, regulatory, finance, and clinical teams.