7 дней назад
Executive Director, Viral Vector Process Development (Cell and Gene Therapy)
255 425 - 330 550$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Executive Director, Viral Vector Process Development (Cell and Gene Therapy): Leading end-to-end viral vector development from construct design through clinical and commercial manufacturing support with an accent on lentiviral vector platforms, process scale-up, technology transfer, and cell therapy integration. Focus on building scalable vector capabilities, guiding CMC and regulatory strategies, and developing a high-performing organization for ex vivo and emerging in vivo applications.
Location: On-site in Santa Monica or Oceanside, California, United States
Salary: $255,425–$330,550 per year, plus potential discretionary bonus, stock-based long-term incentives, paid time off, and benefits.
Company
is a biopharmaceutical company developing CAR and T-cell receptor engineered cell therapies for cancer immunotherapy.
What you will do
- Lead end-to-end viral vector development from construct design through clinical and commercial manufacturing support.
- Set technical strategy for lentiviral vector platforms, including construct architecture, promoter selection, transgene optimization, upstream production, downstream purification, and recovery.
- Drive process scale-up, technology transfer, external manufacturing partnerships, lifecycle management, and manufacturing readiness.
- Advance vector productivity, robustness, cost of goods, in vivo vector development, and emerging delivery technologies.
- Partner with Research, Product Teams, T-cell Process Development, Analytical Development, Technical Operations, and Regulatory functions.
- Build and lead a high-performing viral vector development organization, including laboratories and GMP-adjacent environments.
Requirements
- PhD in Biochemical Engineering, Molecular Biology, Virology, or a related field with 15+ years of experience, or MS with 18+ years.
- Extensive viral vector development and manufacturing support experience in cell and/or gene therapy.
- Expertise in lentiviral and/or retroviral vector systems, analytical characterization, manufacturing, and technology transfer.
- End-to-end experience from early development through commercialization, including cell therapy programs such as CAR-T.
- Strong working knowledge of cGMP regulations, compliance systems, inspection readiness, regulatory filings, and health authority interactions.
- Proven ability to lead large organizations and influence strategic decisions in highly matrixed, cross-functional environments.
Nice to have
- Exposure to in vivo gene delivery platforms.
- Knowledge of retroviral vector development and CMC.
Culture & Benefits
- Mission-driven work focused on developing cancer immunotherapies.
- Emphasis on scientific rigor, accountability, ownership, execution, collaboration, and transparency.
- Medical, dental, vision, and life insurance plans.
- Paid time off and potential discretionary annual bonus and stock-based long-term incentives.
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