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2 дня назад

Project Manager (CapEx Qualification & Infrastructure, Filtration, Med. Device)

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
Project Manager (CapEx Qualification & Infrastructure, Filtration, Med. Device) (Manufacturing Capital Projects): Leading and delivering strategic manufacturing capital, infrastructure, process improvement, and equipment projects in a regulated life sciences environment with an accent on safety, quality, schedule, budget, and compliance. Focus on managing complex cross-functional initiatives, preparing CapEx justifications and financial analyses, and coordinating qualification, validation, and change-control activities.

Location: On-site in Pensacola, Florida, United States; up to 15% potentially international travel.

Company

hirify.global’s Cytiva operating company develops solutions for life sciences, diagnostics, biotechnology, vaccines, medicines, and cell and gene therapies.

What you will do

  • Lead the planning, execution, monitoring, and closure of manufacturing projects using project management methodologies and hirify.global Business System principles.
  • Deliver capital, infrastructure, equipment, process improvement, and operational projects safely, on schedule, within scope and budget, and in compliance with quality and regulatory requirements.
  • Manage project scope, change control, risks, schedules, resources, and budget impacts across multiple concurrent projects.
  • Maintain communication with senior leadership and operational stakeholders on project status, risks, mitigation plans, and business outcomes.
  • Prepare CapEx justifications, financial analyses, budget forecasts, return-on-investment analyses, and executive presentations.

Requirements

  • Bachelor’s degree.
  • Preferred: 3+ years of experience managing large-scale manufacturing, facility, infrastructure, or equipment projects, including budgets exceeding $10 million.
  • Experience leading complex cross-functional projects in manufacturing, engineering, life sciences, medical device, pharmaceutical, biotechnology, or related regulated industries.
  • Strong knowledge of scope management, scheduling, budgeting, resource planning, risk management, and stakeholder management.
  • Strong financial acumen in capital planning, forecasting, return-on-investment analysis, and cost control.
  • Ability to work in an on-site manufacturing environment and follow safety protocols and procedures.

Nice to have

  • Experience with Management of Change processes in regulated manufacturing environments.
  • Experience commissioning, qualifying, and validating manufacturing equipment and facilities.
  • Experience in pharmaceutical, biotechnology, medical device, or life sciences manufacturing operations.

Culture & Benefits

  • Culture focused on belonging, continuous improvement, and life sciences innovation.
  • Paid time off.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) for eligible employees.
  • Eligibility for bonus or incentive pay.

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