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15 часов назад

Principal Scientist, In-vivo CAR-T

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 Scientist, In-vivo CAR-T (Lentiviral Vector Process Development): Developing, optimizing, and scaling lentiviral vector drug product processes from early to late-stage development with an accent on hands-on laboratory work, process characterization, and GMP readiness. Focus on defining robust process design spaces, supporting technology transfer and manufacturing readiness, and applying modelling or machine learning to reduce experimental burden.

Location: On-site in Malvern, Pennsylvania, United States

Company

Johnson & Johnson MedTech develops healthcare innovations and therapies across Innovative Medicine and MedTech.

What you will do

  • Lead, design, and execute lentiviral vector process development studies across early- and late-stage development.
  • Perform hands-on laboratory work involving process design, optimization, and characterization.
  • Analyze and interpret data to improve process understanding, robustness, and decision-making.
  • Support process characterization, including identification of critical process parameters and development of robust processes.
  • Contribute to scale-up, manufacturing readiness, and technology transfer to internal sites or contract manufacturing organizations.
  • Collaborate with Analytical Development, MSAT, Quality, Manufacturing, Regulatory, modelling, and data science teams.

Requirements

  • Ph.D. with 2–4 years of relevant experience, or a B.S./M.S. with 6–8 years of experience in life sciences, chemical engineering, or a related scientific discipline.
  • Experience in viral vector process development and/or lentiviral vector formulation development.
  • Strong hands-on laboratory experience in drug product or viral vector development.
  • Understanding of process scale-up, technology transfer, GxP principles, and data integrity requirements.
  • Strong scientific problem-solving, data interpretation, communication, and prioritization skills.
  • Ability to work effectively and collaborate in a cross-functional, matrixed development environment.

Nice to have

  • Experience with lentiviral vector platforms, viral vectors, or advanced therapies.
  • Familiarity with process validation, including LCPV, and manufacturing support.
  • Exposure to early- and late-stage development or commercial readiness activities.

Culture & Benefits

  • Full-time employment with an inclusive work environment.
  • Cross-functional collaboration across scientific, manufacturing, quality, analytical, and regulatory disciplines.
  • Commitment to equal employment opportunity and an accessible interview process.

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