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2 дня назад

Senior Engineer / Principal Engineer (Lentivirus Downstream Process Development)

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
Senior Engineer / Principal Engineer (Lentivirus Downstream Process Development): Designing, optimizing, and scaling purification processes and process models for lentiviral vectors with an accent on chromatography, tangential flow filtration, analytics, and GMP manufacturing. Focus on building AI-enabled and mechanistic models, translating bench-scale processes to clinical production, and implementing advanced process control strategies.

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

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

Company

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

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 process analytics.
  • Develop clarification, chromatography, and tangential flow filtration workflows to improve vector recovery, purity, and potency.
  • Translate bench-scale processes to GMP manufacturing, lead technology transfer, and provide troubleshooting support during clinical production.
  • Design advanced process control strategies, including model predictive control and state estimators.
  • Author and review development reports, SOPs, and CMC documentation while collaborating with upstream, analytical, manufacturing, and external CDMO teams.

Requirements

  • PhD or MS in Chemical Engineering, Biomedical Engineering, Bioprocess Engineering, or a related field.
  • At least 6 years of experience with a PhD or 8 years with an MS in biotech or pharmaceutical process development or manufacturing.
  • Strong experience in downstream process development, purification, chromatography, and tangential flow filtration.
  • Knowledge of bioprocess modeling and simulation; experience with Python and/or MATLAB.
  • Understanding of GMP manufacturing and CMC strategies for clinical-stage products.
  • English required; applicants must be authorized to work in the United States.

Nice to have

  • Experience with lentiviral vectors, viral vectors, biologics, gene therapy, or advanced therapy process development.
  • Experience developing vector processes for in vivo CAR-T generation and systemic delivery.
  • Experience with purification processes at more than 50 L scale.
  • Mandarin language skills.

Culture & Benefits

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

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