Fully understand the equipment development procedure WE0179 and associated deliverables including ERR, ESRR, EFMEA, and WRAPS/Safety/Ergo assessments.
Delivers robust assembly process and associated equipment that achieves cycle time, cost, capacity, and quality requirements (MSA, GRR).
Continues ownership and support of equipment beyond IQ/OQ/PQ qualification and throughout stabilization period.
This includes handling scrap and supply disruptions, equipment/process improvement projects, and overall stabilization of process while ramping up production prior to LCE/Plant handoff.
Provides significant input to the capital budget estimate.
Understand the connection between product requirements to each assembly station.
Generate equipment requirements.
Leads the DFA assessment for each assigned station, provides feedback to the design team.
Oversight and leadership of the process characterization strategy for each assigned station.
Delivers component, assembly, and supply chain strategy project deliverables at each phase of the project.
Drive critical product requirements cascading to component and assembly processes.
Understand how to transform design information (component drawings and models, product requirements, AFMEA, DFMEA) into a robust manufacturing process.
Identifies and escalates potential development related risks and provides input to the project RISDA.
Develops strategies to mitigate those risks.
Proactively develops strategies to rapidly react to design changes and provide flexibility through use of standardized/family tools, insert strategies, modularity, etc.
Provides critical input to the development of the project schedule, expense and capital budgets.
This may include capital tooling and qualification costs and schedules.
Assists the LDE and Project Director with identifying required development resources.
Escalates needs appropriately to help with prioritization of development team tasks.
Acts as the liaison between the Design team and the component/equipment suppliers.
Provides "voice of manufacturing" to influence design and include DFM/DFA feedback while maintaining Design Intent.
Requirements:
Mechanical, Manufacturing, or Industrial Engineer with 5-10 years of experience in medical device equipment development and manufacturing.
Expertise in assembly equipment development, process validation (IQ/OQ/PQ), DFM/DFA, MSA, Gage R&R, FMEA, and process characterization.
Proven ability to develop robust manufacturing processes, manage equipment suppliers, support product commercialization, and drive continuous improvements in GMP, ISO 13485, and FDA-regulated environments. Strong cross-functional collaboration, technical problem-solving, and risk management skills..
Knowledgeable about medical specific assembly technologies, the equipment supplier base and the capabilities of the suppliers.
Knowledgeable about equipment cost and lead time.
Equipment design, development, FAT, commissioning, and manufacturing automation.
B.E./B.Tech in Mechanical, Manufacturing, or Industrial Engineering with 5-10 years of experience in medical device manufacturing and equipment development.
ICONMA is a global information consulting management firm providing Professional Staffing Services and Project-Based Solutions for organizations in a broad range of industries.
Corporate Headquarters in Troy, Michigan; 20+ locations worldwide.
Certified Woman-Owned Business Enterprise (WBE); certified by Women’s Business Enterprise National Council, National Women Business Owners Corporation (NWBOC); and California Public Utilities Commission (CPUC).
Founded in 2000
2000+ Employees
The company was founded on the principle that success is derived from delivering high quality service and resources in the most responsive, flexible, and innovative way. ICONMA invests in people and resources with a single goal: To provide our customers with the highest quality service in the most responsive manner. Through its network of offices, ICONMA provides the resources to help clients maintain their competitive advantage.
Skills
Assemblers Technologyunmatched
Assembly Equipmentunmatched
Capacity Requirements Planning (CRP)unmatched
Capital Budgetingunmatched
Capital Expenditure (CAPEX)unmatched
Commissioningunmatched
Component Assemblyunmatched
Continuous Improvementunmatched
Cross-Functionalunmatched
Design Failure Mode and Effects Analysis (DFMEA)unmatched
Establish Prioritiesunmatched
FDA (Food and Drug Administration)unmatched
Failure Mode and Effects Analysis (FMEA)unmatched
GMP (Good Manufacturing Practices)unmatched
Health Planunmatched
ISO (International Organization for Standardization)unmatched
Industrial Engineeringunmatched
Information Technology Consultingunmatched
Leadershipunmatched
Machine Toolunmatched
Manufacturingunmatched
Manufacturing Automationunmatched
Manufacturing Process Management (MPM)unmatched
Manufacturing/Industrial Processesunmatched
Medical Equipmentunmatched
Problem Solving Skillsunmatched
Process Improvementunmatched
Process Validationunmatched
Product Supportunmatched
Product/Service Launchunmatched
Project Developmentunmatched
Risk Managementunmatched
Schedule Developmentunmatched
Software Validationunmatched
Strategic Planningunmatched
Supply Chainunmatched
Vendor/Supplier Managementunmatched
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