2 дня назад
Senior Engineer / Principal Engineer (Lentivirus Downstream Process Development)
146 410 - 192 164$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Engineer / Principal Engineer (Lentivirus Downstream Process Development): Designing, optimizing, and scaling purification processes and process models for lentiviral vectors with an accent on chromatography, tangential flow filtration, analytics, and GMP manufacturing. Focus on building AI-enabled and mechanistic models, translating bench-scale processes to clinical production, and implementing advanced process control strategies.
Location: Somerset, New Jersey, United States; onsite. Applicants must be authorized to work in the United States and employment eligibility will be verified through E-Verify.
Base pay: $146,410–$192,164 USD per year, plus performance-based bonus and/or equity for eligible roles.
Company
is a biotechnology company developing cell and gene therapy technologies, including CAR-T, TCR-T, NK cell-based therapies, and lentiviral vector platforms.
What you will do
- Design, optimize, and scale downstream purification processes for lentiviral vectors.
- Build mechanistic, hybrid, and in silico process models using engineering principles, machine learning, and process analytics.
- Develop clarification, chromatography, and tangential flow filtration workflows to improve vector recovery, purity, and potency.
- Translate bench-scale processes to GMP manufacturing, lead technology transfer, and provide troubleshooting support during clinical production.
- Design advanced process control strategies, including model predictive control and state estimators.
- Author and review development reports, SOPs, and CMC documentation while collaborating with upstream, analytical, manufacturing, and external CDMO teams.
Requirements
- PhD or MS in Chemical Engineering, Biomedical Engineering, Bioprocess Engineering, or a related field.
- At least 6 years of experience with a PhD or 8 years with an MS in biotech or pharmaceutical process development or manufacturing.
- Strong experience in downstream process development, purification, chromatography, and tangential flow filtration.
- Knowledge of bioprocess modeling and simulation; experience with Python and/or MATLAB.
- Understanding of GMP manufacturing and CMC strategies for clinical-stage products.
- English required; applicants must be authorized to work in the United States.
Nice to have
- Experience with lentiviral vectors, viral vectors, biologics, gene therapy, or advanced therapy process development.
- Experience developing vector processes for in vivo CAR-T generation and systemic delivery.
- Experience with purification processes at more than 50 L scale.
- Mandarin language skills.
Culture & Benefits
- Medical, dental, and vision insurance with a 401(k) plan and company match.
- Eight weeks of paid parental leave after three months of employment.
- Paid vacation, personal and sick time, floating holidays, and eleven company holidays.
- Additional flexible spending, health savings, disability, life insurance, commuter, family care, and well-being benefits.
- Benefits are available exclusively to permanent full-time employees; contractors are not eligible.
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