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46 минут назад

Senior Scientist – Lentiviral Vector Upstream Process Development (Lentiviral Vector)

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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TL;DR
Senior Scientist – Lentiviral Vector Upstream Process Development (Lentiviral Vector): Developing and optimizing scalable cell culture and bioreactor processes for lentiviral products supporting cell therapy and CAR-T programs with an accent on process characterization, platform robustness, and scale-up. Focus on designing complex experiments, analyzing process data with statistical and visualization tools, transferring bioprocesses to manufacturing sites, and mentoring junior scientists.

Location: Spring House, Pennsylvania, United States of America

Company

Johnson & Johnson MedTech develops healthcare solutions across Innovative Medicine and MedTech.

What you will do

  • Design, execute, and provide scientific guidance for upstream process development studies for lentiviral therapeutic products.
  • Run cell culture experiments using shake flasks, bench-scale bioreactors, and automated high-throughput systems.
  • Improve lentiviral process productivity, quality, manufacturability, robustness, and development efficiency.
  • Support technology transfer to manufacturing sites, commercial manufacturing investigations, and product life cycle management.
  • Apply statistical experimental design, data analytics, online monitoring, and visualization tools to strengthen process understanding.
  • Collaborate with downstream, analytical, formulation, modeling, and automation functions; mentor junior scientists and author technical and regulatory-supporting documents.

Requirements

  • PhD in Chemical Engineering, Biochemical Engineering, Biological Sciences, Biotechnology, or a related field with 2+ years of relevant experience, or BS/MS with 4–6 years of relevant experience.
  • Experience developing processes for viral-based products and mammalian cell culture processes for biologics, cell and gene therapy, RNA therapeutics, or related viral-vector modalities.
  • Hands-on experience with cell culture, bioreactor operation, media optimization, process monitoring, and process scale-up.
  • Strong data analysis, experimental design, technical documentation, written communication, and verbal communication skills.
  • Ability to independently design, execute, interpret, and communicate complex studies in cross-functional teams.
  • Occasional weekend work and up to 10% domestic and international travel may be required.

Nice to have

  • Experience transferring bioprocesses to clinical or commercial GMP manufacturing.
  • Experience with JMP, MiniTab, Python, Spotfire, or similar data analysis and visualization platforms.
  • Knowledge of emerging upstream technologies that improve process robustness and development efficiency.

Culture & Benefits

  • Inclusive work environment centered on individual dignity, diversity, and merit.
  • Opportunity to contribute to cell therapy and CAR-T programs across early- and clinical-stage development.
  • Cross-functional collaboration across process development, manufacturing, analytics, formulation, modeling, and automation.
  • Scientific leadership opportunities across programs and workstreams.

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