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5 дней назад

Principal Engineer, Lentivirus Downstream Process Development (Biotechnology)

146 410 - 192 164$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
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
Principal Engineer, Lentivirus Downstream Process Development (bioprocess modeling and purification): Designing, optimizing, and scaling lentiviral vector purification processes for GMP manufacturing with an accent on mechanistic and hybrid modeling, analytics, and process automation. Focus on translating bench-scale processes to clinical production, implementing advanced process control, and maximizing vector recovery, purity, and potency.

Location: Onsite in Somerset, New Jersey, United States. Applicants must be authorized to work in the United States; employment eligibility is verified through E-Verify.

Base pay: $146,410–$192,164 USD annually, plus performance-based bonus and/or equity for eligible roles.

Company

hirify.global is a biotechnology company developing cell therapies, including CAR-T, TCR-T, NK-cell therapies, and lentiviral vector technologies.

What you will do

  • Design, optimize, and scale downstream purification processes for lentiviral vectors.
  • Build mechanistic, hybrid, and in silico process models using engineering principles, machine learning, and data analytics.
  • Develop downstream workflows covering clarification, depth filtration, centrifugation, chromatography, and tangential flow filtration.
  • Translate bench-scale processes to GMP manufacturing through simulation, laboratory work, technology transfer, and clinical production support.
  • Implement advanced process control strategies, including model predictive control and state estimators.
  • Lead scientists, author technical and regulatory documents, and collaborate with upstream, analytical, CMC, project, and external manufacturing teams.

Requirements

  • PhD preferred, or MS, in Chemical Engineering, Biomedical Engineering, Bioprocessing Engineering, or a related field.
  • At least 8 years of experience with a PhD or 10 years with an MS in biotech or pharmaceutical process development or manufacturing.
  • Strong knowledge of bioprocess modeling and simulation, biomolecule interactions, and process engineering.
  • Experience with Python and MATLAB, plus deep technical expertise in purification, chromatography, and TFF.
  • Strong understanding of GMP manufacturing requirements and CMC strategies for clinical trials, with deep knowledge of lentiviral vector technologies.
  • English is required, and applicants must already be authorized to work in the United States.

Nice to have

  • Experience developing vector processes for in vivo CAR-T generation and systemic delivery.
  • Experience with large-scale purification processes above 50 liters.
  • Mandarin language skills.

Culture & Benefits

  • Medical, dental, and vision insurance with a 401(k) company match that fully vests on day one.
  • Eight weeks of paid parental leave after three months of employment.
  • Paid vacation, personal and sick time, floating holidays, and eleven company holidays.
  • Additional spending accounts, disability and life insurance, commuter benefits, family-care resources, and well-being programs.
  • Benefits are available exclusively to permanent full-time employees; contractors are not eligible.

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