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4 часа назад

Project Engineer III (Pharmaceutical Manufacturing)

125 000 - 135 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/Switzerland
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 Engineer III (Pharmaceutical Manufacturing) (CAPEX/CQV/GMP): Leading capital projects for pharmaceutical manufacturing operations, including facility expansions, utility upgrades, equipment implementation, and new product introductions with an accent on commissioning, qualification, validation, and regulatory compliance. Focus on managing complex projects from concept through startup, coordinating cross-functional stakeholders and vendors, and improving manufacturing capacity and performance in cleanroom environments.

Location: Irvine, California, United States; onsite

Salary: $125,000–$135,000 per year

Company

hirify.global is a global pharmaceutical CDMO that develops and manufactures APIs and finished dosage forms across 16 sites on three continents.

What you will do

  • Lead CAPEX projects covering facility expansions, utility upgrades, equipment installations, and manufacturing process improvements.
  • Manage projects from concept through commissioning, qualification, validation, and operational handoff.
  • Develop project plans, budgets, schedules, and risk mitigation strategies.
  • Coordinate contractors, vendors, OEMs, and cross-functional Manufacturing, Quality, Validation, and Facilities stakeholders.
  • Lead FAT, SAT, and CQV activities, including URS, DQ, IQ, OQ, and PQ documentation.
  • Support new product introductions, process optimization, equipment lifecycle management, root cause investigations, CAPAs, and continuous improvement.

Requirements

  • Bachelor’s degree in Mechanical, Chemical, Industrial, Pharmaceutical, or related Engineering discipline.
  • At least 4 years of engineering experience in pharmaceutical, biotechnology, medical device, or other highly regulated manufacturing environments.
  • At least 2 years of direct Commissioning, Qualification, and Validation experience.
  • Proven experience managing CAPEX projects and implementing manufacturing equipment.
  • Strong understanding of GMP manufacturing, validation, FDA requirements, and quality systems.
  • Experience working in cleanroom environments.

Nice to have

  • Experience in a CDMO environment.
  • Experience supporting new product introductions and manufacturing scale-up.
  • Experience working directly with vendors, contractors, and regulatory auditors.

Culture & Benefits

  • Medical, dental, and vision insurance.
  • Flexible Spending Account and HSA options.
  • Life insurance and short- and long-term disability coverage.
  • Pet insurance.
  • 401(k) plan.
  • Collaborative environment focused on safety, quality, sustainability, and professional growth.

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