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21 час 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 concept development, detailed design, and implementation with an accent on process calculations, PFDs, P&IDs, equipment specifications, and GMP compliance. Focus on analyzing complex technical challenges, designing compliant process solutions, and coordinating engineering deliverables across multidisciplinary project teams.

Location: Clayton, North Carolina, United States; must be based in Clayton

Salary: Competitive salary with annual adjustment increases

Company

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

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 quality, budget, and schedule expectations.
  • Collaborate with multidisciplinary teams, clients, vendors, and subject matter experts on practical and compliant process solutions.
  • Analyze technical challenges, evaluate alternatives, and recommend solutions supporting client and project objectives.
  • Contribute to knowledge sharing, process improvements, and engineering best practices.

Requirements

  • Must be based in Clayton, North Carolina, United States.
  • Must have unrestricted authorization to work in the United States and must not require current or future employer sponsorship.
  • Bachelor's or master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related discipline.
  • At least 3 years of relevant engineering experience in pharmaceutical, biotechnology, life sciences, or another regulated industry.
  • Experience with process calculations, PFDs, P&IDs, equipment sizing, and technical documentation.
  • Familiarity with GMP-regulated environments and pharmaceutical manufacturing processes, plus strong communication and collaboration skills.

Nice to have

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

Culture & Benefits

  • Agile, fast-paced, project-oriented environment with multidisciplinary collaboration.
  • 160 hours of paid time off, prorated from the hire date, plus 14 paid holidays.
  • Health, dental, and vision insurance from the first day.
  • 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 system only.
  • Interviews are scheduled on a rolling basis.
  • Application deadline: September 25, 2026.

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