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5 дней назад

Industrial Engineer I (Medical Devices)

68 000 - 102 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Industrial Engineer I (Medical Devices): Supporting continuous improvement and operational excellence across medical device manufacturing operations with an accent on Lean, Six Sigma, process analysis, and data-driven decision-making. Focus on analyzing workflows, optimizing layouts and material flow, conducting time and capacity studies, and implementing standardized processes that improve productivity and reduce waste.

Location: Fridley, Minnesota, United States; minimum 5 days per week onsite at the Brooklyn Park site.

Salary: $68,000–$102,000 per year, plus eligibility for the hirify.global Incentive Plan.

Company

hirify.global develops healthcare technologies that aim to alleviate pain, restore health, and extend life.

What you will do

  • Analyze manufacturing processes, workflows, and operational metrics to identify improvement opportunities.
  • Support initiatives that increase throughput and productivity, reduce waste and costs, and improve process flow.
  • Conduct time studies, capacity analyses, and labor utilization studies for operational decision-making.
  • Support facility layout, equipment utilization, workspace, and material flow optimization.
  • Develop standardized work, visual management systems, and process controls.
  • Collaborate with manufacturing, quality, supply chain, and engineering teams on sustainable solutions.

Requirements

  • Bachelor’s degree and 0–2 years of relevant experience.
  • Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for roles below Principal level.
  • Ability to work onsite at least five days per week.
  • Knowledge of Lean Manufacturing and Six Sigma methodologies is beneficial.
  • Experience with time studies, capacity analysis, process mapping, facility layout, or material flow optimization is beneficial.
  • For degrees earned outside the United States, the degree must satisfy the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).

Nice to have

  • Experience in regulated medical device, pharmaceutical, or biotechnology manufacturing.
  • Experience supporting manufacturing process improvement or cost reduction projects.
  • Experience with Microsoft Excel, Power BI, Minitab, SAP, or AutoCAD.

Culture & Benefits

  • Cross-functional, in-person collaboration in a highly regulated manufacturing environment.
  • Health, dental, and vision insurance, plus health and dependent-care spending accounts.
  • 401(k) plan with employer contribution and match, paid time off, and paid holidays.
  • Life insurance, disability coverage, tuition assistance, employee stock purchase plan, and employee assistance resources.

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