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10 дней назад

End to End Project Lead (Pharmaceutical Manufacturing)

181 500 - 302 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
US
Релокация
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
End to End Project Lead (Pharmaceutical Manufacturing): Planning and delivering design, construction, commissioning, validation, and technology transfers for product-agnostic manufacturing capabilities with an accent on cost, scope, schedule, and cGMP compliance. Focus on leading complex asset-modification projects, coordinating cross-functional engineering and procurement activities, and ensuring operational readiness for regulatory approval.

Location: Vacaville, California, United States. This is a fully site-based role requiring in-person work. Relocation assistance is available for eligible candidates and their families.

Salary: $181,500–$302,000 base annual salary, plus a performance-related bonus.

Company

hirify.global operates a globally connected network of life sciences manufacturing sites producing medicines and supporting pharmaceutical innovation.

What you will do

  • Define project scope, goals, economic justification, and alignment with market strategy.
  • Lead the design, construction, commissioning, and validation of existing asset modifications.
  • Manage cost, scope, schedules, contractual frameworks, and project governance.
  • Coordinate downtime planning, CAPEX, procurement, technology transfers, and cross-functional validation.
  • Build and mentor high-performing project teams while facilitating communication between engineering and steering committees.
  • Lead operational readiness and mitigation plans to support cGMP compliance and regulatory approval.

Requirements

  • Bachelor’s degree in Life Science, Engineering, or Business Management; a master’s degree is preferred.
  • 10+ years of experience in manufacturing or operations within the pharmaceutical, biopharmaceutical, or another regulated industry.
  • Demonstrated operational management and project delivery experience.
  • Strong understanding and proven experience with cGMP requirements for biologics manufacturing.
  • Data-driven decision-making and strong problem-solving skills.
  • Understanding of operational excellence and continuous improvement methodologies, including Lean and Six Sigma.

Nice to have

  • PMP Project Manager Certification.
  • 6S or Lean Manufacturing experience.
  • Lean Six Sigma Green Belt or Black Belt.

Culture & Benefits

  • Performance-related bonus.
  • Medical, dental, and vision insurance.
  • 401(k) matching plan.
  • Life insurance and short- and long-term disability insurance.
  • Employee assistance programs and paid time off.
  • Collaborative, accountable, excellence-focused, and inclusive work environment.

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