- Participate in the design, execution, and support of laboratory studies for development, optimization, and manufacture of genome engineered TCR T-cell products using non-viral genome editing tools.
- Execute and support analytical methods for process development studies.
- Support experimental designs, planning, execution, analysis, and reporting results of process development studies.
- Participate in a cross-functional team to transfer technology to cGMP manufacturing partners.
- Support, author, and review protocols, technical reports, regulatory documents, and memos to summarize experiments and investigations.
- Collaborate with internal and external partners to evaluate and implement new process technologies to develop next generation processes.
- Collaborate within the project team to interpret study results and contribute to technical discussions for subsequent study design.
- Work effectively in a team environment to meet project timeline and objectives.
- Oversee Junior associates in execution of development activities.
- Perform other duties as assigned.
- Bachelors in relevant life science field with 4+ years of industry experience, Masters with 2+ years of experience, or PhD with 0+ years of experience
- 3+ years of experience in developing production processes for genome engineered primary cells
- T-cell experience highly preferred
- 2+ years of experience working with multi-color Flow Cytometry
- T-cell characterization experience highly preferred
- Experience performing various analytical methods used in manufacturing and characterization of products.
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