No more applications are being accepted for this job
- 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.
- MS degree in Immunology, Cell Biology, Molecular biology, Bioengineering with 2+ years relevant experience or similar BS degree with 4+ years relevant experience within the pharmaceutical or biotech industries.
- At least 3 years of relevant experience in developing production processes for genome engineered primary cells (required) including T cells (highly preferred).
- A minimum of two (2) years practical experience with Flow Cytometry.
- Hands-on experience performing analytical methods typically used in the manufacture and characterization of biological products.
Principal Research Associate, Process Development - Santa Monica, United States - GQR
Description
Title: Principal Research Associate, Process Development
Status: Full-time direct hire
Location: Onsite Monday through Friday in Santa Monica, CA
Compensation: $90,000 to $100,000 per year
The Principal Research Associate, Process Development is responsible for supporting and contributing to the design and execution of studies to develop and further optimize clinical manufacturing processes of engineered TCR T cell therapies.
Other duties:
Required Skillsets:
Please note, this role is not set up for Visa sponsorship or transfer now, or in the future.