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22 часа назад

Operational Excellence Manager (Medical Devices)

90 500 - 135 800$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Operational Excellence Manager (Lean Manufacturing/Medical Devices): Leading site-wide continuous improvement initiatives across regulated manufacturing operations with an accent on Lean Six Sigma, Kaizen events, OEE improvement, capacity increases, and cost reduction. Focus on analyzing plant processes, developing standard work, facilitating cross-functional problem-solving, and coaching teams in operational excellence methods.

Location: Onsite at the manufacturing facility in Acton, Massachusetts, United States

Annual base salary: $90,500–$135,800, with potential incentive compensation.

Company

hirify.global is a medical device company developing the Omnipod insulin management platform and other subcutaneous drug delivery products.

What you will do

  • Lead strategic continuous improvement initiatives across manufacturing and operational departments.
  • Drive Lean Manufacturing practices, including Kaizen, Value Stream Mapping, 5S/6S, PDCA, and DMAIC.
  • Develop and sustain standard work processes that improve safety, quality, productivity, and efficiency.
  • Identify improvements that increase capacity, improve OEE, and reduce manufacturing costs.
  • Facilitate cross-functional problem-solving, track project progress, and communicate results to leadership.
  • Analyze plant layout, equipment, workflow, and operational practices; manage project budgets and coach employees in Lean Six Sigma principles.

Requirements

  • Bachelor's degree in Engineering or a related technical discipline.
  • 3+ years of project management experience in a manufacturing or technical environment.
  • Six Sigma Green Belt certification and experience applying Lean Manufacturing and continuous improvement methodologies.
  • Knowledge of U.S. and international medical device and drug delivery regulations.
  • Strong project management, organizational, communication, influencing, and presentation skills.
  • Ability to work onsite, stand and walk for up to 75% of the workday, lift up to 25 pounds, and support off-shift operations when required.

Nice to have

  • Experience in medical device manufacturing or other regulated industries.
  • Working knowledge of ISO 13485, ISO 14971, IEC 62304, and FDA 21 CFR Part 820.
  • Experience with Microsoft Project, Excel, PowerPoint, Word, and SolidWorks.
  • Experience working in a fast-paced, growth-oriented manufacturing environment.

Culture & Benefits

  • Lead operational transformation initiatives with measurable business impact.
  • Collaborate with cross-functional teams and influence manufacturing strategy.
  • Medical, dental, and vision insurance.
  • 401(k) with company match.
  • Paid time off and employee wellness programs.

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