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1 день назад

Project Manager - Manufacturing Engineering (Medical Devices)

88 500 - 110 700$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Project Manager - Manufacturing Engineering (Medical Devices): Managing manufacturing engineering projects from planning through execution, including schedules, budgets, resources, risks, and quality plans with an accent on equipment and process validation, pFMEA, and regulated medical-device production. Focus on identifying critical paths, resolving roadblocks, tracking financial and project KPIs, and coordinating stakeholders to deliver within scope, schedule, and budget.

Location: Pawtucket, Rhode Island, United States

Salary: $88,500–$110,700 per year, plus eligibility for an annual bonus.

Company

ZOLL develops medical devices, software, and related services for diagnosing and treating serious cardiopulmonary and respiratory conditions, serving customers in more than 140 countries.

What you will do

  • Manage project planning, resource coordination, scheduling, budgeting, execution, and reporting within Manufacturing Engineering.
  • Prepare project plans, schedules, budgets, and primary project documentation using project management tools.
  • Communicate project status, roles, expectations, and accountabilities to stakeholders and team members throughout the project lifecycle.
  • Assign tasks, track schedules, identify risks and critical paths, and develop contingency plans to resolve roadblocks.
  • Develop project and financial KPIs and maintain current cost and schedule information.
  • Work with Quality to develop and execute project quality plans using standard development methodologies.

Requirements

  • Bachelor’s degree in Engineering or a related field.
  • 3–5 years of project management experience in medical devices or comparable experience.
  • Working knowledge of equipment and process validation and pFMEA development.
  • Strong background in ISO 13485, ISO 9001, and FDA 21 CFR 820.
  • Strong communication, time management, financial, and accounting skills.
  • Must be eligible to work in the United States; immigration-related sponsorship is not available now or in the future.

Nice to have

  • PMP certification from PMI.

Culture & Benefits

  • Work focused on improving outcomes for patients with critical cardiopulmonary and respiratory conditions.
  • Culture emphasizing innovation, self-motivation, and an entrepreneurial spirit.
  • Eligibility for an annual bonus under the company bonus plan.
  • Comprehensive benefits plans.

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