20 часов назад
Sr. Scientist, Lentivirus Upstream Processing
127 313 - 167 099$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr. Scientist, Lentivirus Upstream Processing (Lentivirus/Cell Therapy): Designing and optimizing upstream production processes for lentiviral vectors using mammalian cell culture, transient transfection, and bioreactors with an accent on scalable, robust, and phase-appropriate GMP manufacturing. Focus on bioreactor scale-up and scale-down modeling, technology transfer, process troubleshooting, and optimizing vector titer, productivity, and quality.
Location: Hybrid role based in Somerset, New Jersey, United States
Salary: $127,313–$167,099 USD annual base pay, plus potential performance-based bonus and/or equity.
Company
is a global biotechnology company developing cell therapy platforms, including CAR-T, CAR-NK, CAR-γδ T, and other emerging technologies.
What you will do
- Design and execute experimental strategies for lentiviral vector upstream production.
- Develop and optimize seed train expansion, HEK293/HEK293T mammalian cell culture, transient transfection, feeding strategies, and perfusion processes.
- Develop and validate bioreactor scale-up and scale-down models using stir-tank and rocker systems.
- Translate bench-scale processes to GMP manufacturing, support technology transfer, and troubleshoot clinical production runs.
- Optimize vector titer, specific productivity, and product quality while documenting process parameters and performance limits.
- Prepare development reports, SOPs, and regulatory submission content, and collaborate with CMC, downstream, analytical, and external CDMO teams.
Requirements
- Advanced degree, preferably PhD or MS, in Chemical Engineering, Bioengineering, or a related field.
- 5–8 years of experience with a PhD or 8+ years with an MS in biotech or pharmaceutical process development or manufacturing.
- Hands-on experience with HEK293/HEK293T culture, seed train expansion, feeding strategies, and viral-vector transient transfection optimization.
- Experience developing and implementing bioreactor scale-up and scale-down models, with knowledge of engineering modeling, mass transfer, and bioprocess optimization.
- Understanding of GMP manufacturing requirements and CMC strategies for early-phase clinical trials.
- Applicants must be authorized to work in the United States; employment eligibility is verified through Form I-9 and E-Verify.
Nice to have
- Experience with lentiviral vector technologies and large-scale upstream bioreactor processes above 50L, including 200L or 500L systems.
- Mandarin language skills.
Culture & Benefits
- Hybrid work environment within a global biotechnology organization.
- Medical, dental, and vision insurance with a 401(k) plan and company match vesting fully on day one.
- Eight weeks of paid parental leave after three months of employment.
- Paid vacation, personal and sick time, floating holidays, and eleven company holidays.
- Additional health, disability, commuter, family-care, well-being, and recognition benefits are available to permanent full-time employees.
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