1 час назад
Scientist, In Vivo Process Development Downstream (Lentivirus)
133 195 - 172 370$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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