Equipment Engineer

ICONMA, LLC

  • Cincinnati, OH
  • 3 days ago
  • $35.71 Per Hour

Highlights

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. 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.

Numbers & Facts

LocationCincinnati, OH
Salary$35.71 Per Hour

Description

Our client, a IT Services and Consulting company, is looking for a Equipment Engineer for their Cincinnati, OH location.
 
Responsibilities:

  • Fully understand the equipment development road map (TR011027).
  • Understand equipment concept creation, review approval, build, run off, FAT, software validation, IQ, OQ, PQ road map requirements.
  • 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.
  • Medical domain experience
  • Years of Experience: 10.00 Years of Experience
 
Why Should You Apply?

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