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Scientist, In Vivo Process Development Downstream (Lentivirus)

133 195 - 172 370$
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
Scientist, In Vivo Process Development Downstream (Lentivirus): Designing and executing downstream purification experiments for scalable Lentivirus manufacturing processes with an accent on chromatography, filtration, scale-up, and process optimization. Focus on applying statistical methodologies, solving complex bioprocess problems, and providing technical leadership while mentoring colleagues.

Location: Philadelphia, Pennsylvania, United States

Salary: $133,195–$172,370 per year, plus potential annual bonus, stock-based incentives, paid time off, and benefits.

Company

hirify.global develops cancer immunotherapies, including CAR T-cell and T-cell receptor engineered cell therapies.

What you will do

  • Design and optimize scalable, safe, and cost-effective downstream processes for Lentivirus manufacturing.
  • Develop technical solutions using advanced chemistry, biochemistry, engineering, statistical, and modelling principles.
  • Support manufacturing activities, process scale-up, and optimization of large-biomolecule processes.
  • Manage day-to-day laboratory operations, documentation, data analysis, and safety compliance.
  • Prepare technical reports and presentations while collaborating with multidisciplinary groups.
  • Train, guide, mentor, and technically support colleagues in process execution and troubleshooting.

Requirements

  • BS with 6+ years of relevant post-graduate experience, MS with 4+ years, or PhD/PharmD in science, engineering, bioprocessing, or biotechnology.
  • Hands-on proficiency with downstream unit operations for large biomolecules, including chromatography and filtration.
  • Understanding of bioprocess scale-up principles and cGMP practices.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and data analysis tools such as JMP or GraphPad.
  • Strong collaboration, communication, organization, problem-solving, and attention-to-detail skills.
  • Onsite work in Philadelphia, Pennsylvania, United States is required.

Nice to have

  • Experience developing viral vector processes.
  • Experience using Design of Experiments for process development.
  • Experience with fermentation, cell culture, large-biomolecule analysis, or large-scale bioprocessing in GMP or non-GMP settings.
  • Mentorship and team leadership experience.

Culture & Benefits

  • Full-time employment within a cancer-immunotherapy organization.
  • Medical, dental, vision, and life insurance plans.
  • Paid time off and potential annual bonus and stock-based long-term incentives.
  • Inclusive work environment focused on collaboration, development, and employee empowerment.

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