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Quality Assurance Analyst (Regulatory) CVPF (Center for Cellular Immunotherapy)
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- The Quality Assurance Analysis will work within the Clinical Cell and Vaccine Production Facility (CVPF) for the review and release of investigational cell and gene therapy products for human administration manufactured at our facility.
- Communicate errors and deviations identified during batch record review.
- Conduct apheresis product receipt of fresh and frozen apheresis product collected and cryopreserved by CCI internal and external multi-center sites.
- Coordinate and follow-up with apheresis collection and cryopreservation site for addressing all observations during the receipt.
- 1-3 years of experience in a GLP/GCP/GMP setting, or equivalent, with >1 year of direct experience in Quality role
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