46 минут назад
Senior Scientist – Lentiviral Vector Upstream Process Development (Lentiviral Vector)
Мэтч & Сопровод
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Описание вакансии
Текст:
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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