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5 дней назад

Senior Director, Project Engineering (Biologics and Cell & Gene Therapy)

206 500 - 393 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior/director
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
Senior Director, Project Engineering (Biologics and Cell & Gene Therapy): Establishing engineering strategy, standards, governance, and project delivery for biologics drug substance and cell and gene therapy manufacturing investments with an accent on process platform deployment, facility development, technical assurance, and manufacturing technology interfaces. Focus on leading technical decisions across capital projects and manufacturing sites, integrating cross-functional stakeholders, and building consistent engineering practices for safety, quality, compliance, scale-up, and operational readiness.

Location: North Chicago, Illinois, United States

Base salary: USD 206,500–393,000 per year

Company

hirify.global develops medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Establish and deploy global engineering standards, technical practices, governance expectations, and engineering requirements for biologics drug substance and cell and gene therapy manufacturing.
  • Provide engineering leadership for new manufacturing facilities, production capabilities, strategic capacity projects, technology platforms, and lifecycle technology upgrades.
  • Support front-end engineering, facility concept development, investment evaluation, manufacturing capability assessments, and site and platform planning.
  • Lead technical decision-making and coordinate engineering input across manufacturing sites, project teams, suppliers, vendors, and external engineering partners.
  • Integrate engineering decisions with operations, quality, validation and CQV, EHS, supply chain, finance, regulatory expectations, and site handover needs.
  • Build technical capability through coaching, mentoring, knowledge sharing, technical reviews, and continuous improvement.

Requirements

  • Bachelor's degree in engineering, science, or a relevant technical discipline; an advanced degree is preferred.
  • 15+ years of relevant engineering, manufacturing, capital project, technical operations, or regulated manufacturing experience.
  • Technical expertise in biologics drug substance and cell and gene therapy process engineering, process platform deployment, process package design, technical assurance, and project delivery.
  • Experience with regulated biopharmaceutical manufacturing environments such as biologics, cell therapy, gene therapy, viral vectors, mRNA, or sterile biologics.
  • Knowledge of bioreactors, harvest, purification, single-use and closed processing, aseptic processing, viral vectors, cell processing, and cryogenic or cold-chain interfaces.
  • Strong technical judgment, risk management, communication, stakeholder engagement, structured problem-solving, and matrix leadership skills.

Culture & Benefits

  • Collaboration across global functions, manufacturing sites, regions, and external engineering partners.
  • Focus on engineering excellence, safety, quality, reliability, sustainability, accountability, and proactive risk management.
  • Paid time off, vacation and sick leave, holidays, medical, dental, and vision insurance.
  • 401(k) and eligibility for long-term incentive programs.

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