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4 дня назад

Industrial Engineer II (Medical Devices)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Industrial Engineer II (Medical Devices): Analyzing and optimizing manufacturing workflows, facility layouts, equipment utilization, and production performance in a regulated medical technology environment with an accent on capacity planning, material flow, and data-driven process improvement. Focus on improving throughput, reducing waste, supporting compliance, and solving operational challenges across manufacturing, quality, supply chain, and engineering teams.

Location: Juncos, Puerto Rico, United States; onsite work arrangement

Company

hirify.global develops healthcare technologies and medical devices used to improve patient health worldwide.

What you will do

  • Analyze manufacturing processes, workflows, operational metrics, and production performance to identify efficiency improvements.
  • Develop and implement initiatives that improve throughput, reduce waste, and support cost reduction.
  • Conduct capacity planning, labor utilization, inventory control, and production planning analyses.
  • Evaluate facility layouts, equipment utilization, and material flow to improve manufacturing effectiveness.
  • Collaborate with manufacturing, quality, supply chain, and engineering teams to resolve operational challenges.
  • Support safety, quality, regulatory compliance, and continuous improvement initiatives.

Requirements

  • Bachelor’s degree in Industrial Engineering and at least two years of manufacturing or industrial engineering experience, or a master’s degree in Industrial Engineering with no required experience.
  • Experience analyzing manufacturing processes and implementing process improvements.
  • Experience using data analysis techniques to evaluate operational performance and support decisions.
  • Knowledge of production systems, capacity planning, and workflow optimization.
  • Ability to manage multiple priorities while working independently and collaboratively.
  • Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for this role.

Nice to have

  • Experience in regulated medical device, pharmaceutical, or biotechnology manufacturing.
  • Knowledge of Lean Manufacturing and Six Sigma methodologies.
  • Experience with facility layout design, material flow optimization, and equipment utilization studies.
  • Experience with Excel, Power BI, Minitab, SAP, or AutoCAD.
  • Experience supporting cross-functional operational improvement projects.

Culture & Benefits

  • Full-time employment within a healthcare technology organization.
  • Competitive compensation and flexible benefits package.
  • Eligibility for the hirify.global Incentive Plan short-term incentive.
  • Reasonable accommodations are available for qualified individuals with disabilities.

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