- Designing, executing, analyzing, and documenting early and late-stage process development studies.
- Cultivating T cells in various formats, including flasks, bags, and bioreactors.
- Acting as a project/program manager with autonomy and discretion.
- Bachelor's, Master's, or PhD degree in Biochemical Engineering, Biomedical Engineering, Biotechnology, or related fields.
- Minimum of six (6) years with a Bachelor's, four (4) years with a Master's, or one (1) year with a PhD of relevant industry experience.
- Knowledge of cGMP manufacturing and regulations, with practical experience in GMP.
- Hands-on experience in cell and gene therapy, particularly with T cells, is highly desirable.
- Experience in technical development of cell and gene therapy or biologics across early and late-stage development phases.
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Senior Process Development Engineer - California, United States - GQR
Description
Join an innovative global biotech company at the forefront of solid cancer therapy. Our LA-based client pioneers individualized T cell therapies, leveraging tumor mutation profiles to offer new solutions for cancer treatment challenges.
We're seeking a Senior Process Engineer to join a dynamic team in Santa Monica, CA. In this role, you'll be instrumental in developing clinical manufacturing processes for engineered T cells with patient-specific TCRs. Your responsibilities will include designing, executing, and documenting process development studies, ensuring compliance with cGMP standards, and providing support for manufacturing and technology transfer.
Key Responsibilities:
Required Qualifications:
Please note, this role is not set up for Visa sponsorship or transfer now, or in the future.
*By applying for this position, you agree to receive marketing communication from GQR and agree to our GQR Privacy Policy & GQR Terms of Use. You may unsubscribe at any given time.
