Senior Scientist, Cell Therapy Process Development
Quick Summary
GeneFab is seeking a highly skilled Senior Scientist to join our Cell Therapy Process Development team in Alameda, CA. In this role, you will lead the design and optimization of integrated processes,
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Design and perform experiments to optimize integrated processes for cell therapy, including: evaluation of cell sources, isolation and activation of human immune cells, media optimization, viral/non-viral genetic modification, cell expansion, cell harvest/fill/finish, and cryopreservation.
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Cell therapy process scaleup, including: transition from open processes to closed automated systems, understanding analytical methods, using a Design of Experiments (DoE) approach, and evaluating process choices within a Quality by Design (QbD) framework
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Exploration of new technologies or materials for process scale-up or improvements with quality mindset leading to clinical or commercial readiness.
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Cross-functional collaborations in project teams to translate scientific understanding to development of phase appropriate cGMP cell therapy manufacturing unit operations.
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Lead the design, execution, and analysis of experimental studies for new manufacturing technologies and processes
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Author and review study protocols, technical reports, ELNs, regulatory submissions.
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Support authoring of key documentation to enable technology transfer (e.g. sampling plans, batch records, specifications, SOPs, FMEA, flow diagrams, etc.).
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Help coordinate sample management workflow across Process and Analytical Development teams and manage development database
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Serve as a technical resource/SME for GMP operations (e.g. root cause analyses and continuous improvement initiatives)
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Coordinate and prioritize tasks across multiple projects
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Maintain familiarity with current state-of-the-art related to cell therapy processes
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BS/MS with 6+ years or PhD with 4+ years of experience in science/engineering of biopharmaceutical or cell/gene therapy process development and technology transfer
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Hands-on experience with automated cell processing units or platforms (i.e. bioreactors, automated cell wash, fill and finish) is critical.
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Experience developing and optimizing cell therapy processes for GMP production with quality mindset
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Strong technical writing and communication skills to support both development and tech transfer applications
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Strong critical thinking, organizational skills, ability to work in multi-functional project teams, and attention to detail
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Experience with various types of cell therapy products (i.e. CAR-T, CAR-NK, HSC, MSC) is preferred
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Experience with AI solutions for CGT processes and working with LIMS is a plus
Location & Eligibility
Listing Details
- Posted
- May 28, 2026
- First seen
- May 28, 2026
- Last seen
- May 30, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 71%
- Scored at
- May 28, 2026
Signal breakdown
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