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6 дней назад

Labeling Program Lead (Medical Devices)

91 200 - 136 800$
Формат работы
onsite
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

Текст:
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TL;DR
Labeling Program Lead (Medical Devices): Managing labeling activities and deliverables across medical device product lifecycle initiatives with an accent on project planning, cross-functional coordination, and regulatory compliance. Focus on coordinating technical writers, tracking risks and schedules, developing progress dashboards, and improving controlled documentation processes.

Location: Onsite in Minneapolis, Minnesota, United States

Salary: $91,200–$136,800 per year, plus eligibility for the hirify.global Incentive Plan.

Company

hirify.global develops medical technologies and healthcare solutions used worldwide.

What you will do

  • Develop and maintain labeling project plans and schedules aligned with program milestones.
  • Coordinate labeling activities, dependencies, and timelines with cross-functional stakeholders.
  • Manage labeling deliverables from initiation through release and communicate project status.
  • Coordinate work across technical writers and other labeling contributors.
  • Monitor project risks, resource needs, and schedule impacts, escalating issues when needed.
  • Develop dashboards and metrics while supporting process improvement initiatives.

Requirements

  • Bachelor’s degree and at least 2 years of relevant experience.
  • Experience leading or coordinating cross-functional projects with multiple stakeholders.
  • Experience managing project schedules, risks, and deliverables.
  • Experience with Microsoft Project, Smartsheet, or similar project management tools.
  • Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for roles below Principal level.

Nice to have

  • Experience in medical devices, healthcare, life sciences, or another regulated industry.
  • Experience with labeling, technical documentation, or controlled documentation processes.
  • Knowledge of EU MDR, FDA 21 CFR Part 801, or ISO 20417.
  • Experience driving process improvement or operational initiatives.
  • Ability to influence and align stakeholders without direct authority.

Culture & Benefits

  • Health, dental, and vision insurance for eligible regular employees.
  • 401(k) plan with employer contribution and match.
  • Paid time off, paid holidays, and disability coverage.
  • Health Savings Account, Flexible Spending Account, life insurance, and employee assistance program.
  • Tuition assistance or reimbursement and employee stock purchase plan.

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