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5 дней назад

Process Engineering Consultant (Pharmaceutical Manufacturing)

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
Process Engineering Consultant (Pharmaceutical Manufacturing): Developing and optimizing pharmaceutical and biotechnology manufacturing processes through conceptual, basic, and detailed design with an accent on process calculations, PFDs, P&IDs, equipment specifications, and GMP compliance. Focus on analyzing technical challenges, sizing equipment, collaborating with multidisciplinary project teams, and supporting implementation in regulated manufacturing environments.

Location: Clayton, North Carolina, United States; must be based in Clayton. Unrestricted authorization to work in the United States is required, and employer-sponsored work authorization is not available.

Company

hirify.global delivers engineering consulting and project solutions for pharmaceutical, biotechnology, and life sciences manufacturing.

What you will do

  • Develop process engineering deliverables, including process flow diagrams, process descriptions, equipment specifications, calculations, and technical reports.
  • Execute engineering tasks across conceptual, basic, and detailed design phases while meeting project quality, budget, and schedule expectations.
  • Collaborate with multidisciplinary project teams, customers, vendors, and subject matter experts to develop practical and compliant process solutions.
  • Analyze technical challenges, evaluate alternatives, and recommend solutions supporting customer objectives and project delivery.
  • Contribute to knowledge sharing, process improvements, and best practices.

Requirements

  • Willingness and ability to be based in Clayton, North Carolina, and work in an agile, fast-paced, project-oriented environment.
  • Bachelor's or master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.
  • At least 3 years of relevant engineering experience in pharmaceutical, biotechnology, life sciences, or related regulated industries.
  • Experience with process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.
  • Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes.
  • Ability to collaborate with multidisciplinary teams to solve technical challenges and deliver high-quality engineering solutions.
  • Strong communication skills and the ability to build productive relationships with customers and project teams.
  • Proactive mindset, strong attention to detail, commitment to continuous improvement, and willingness to expand technical capabilities through project experience, learning, and feedback.
  • Unrestricted authorization to work in the United States without current or future sponsorship requirements.

Nice to have

  • Experience with commissioning, qualification, validation, or process optimization activities.

Culture & Benefits

  • Collaborative environment with multidisciplinary project teams, customers, and subject matter experts.
  • Competitive salary with annual adjustment increases.
  • 160 hours of PTO, prorated from the hire date, plus 14 paid holidays.
  • Health, dental, and vision insurance from day one.
  • 8% guaranteed 401(k) company contribution.
  • 14 weeks of paid parental leave, company-paid life and disability insurance, and employee referral bonuses.

Hiring process

  • Applications are accepted through the online application system only.
  • Interviews are conducted on a rolling basis.
  • Application deadline: November 6, 2026.

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