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As a Technician I, GMP Manufacturing - Upstream you will play a critical role in the production and cultivation of AAV-based gene therapy products in compliance with current Good Manufacturing Practices (cGMP) regulations.
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A Research Associate to support our therapeutic gene therapy discovery efforts using our proprietary CNS-targeted LNP platform and the CasPlus gene editing system, while also helping the team manage the laboratory.
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As a leading biotechnology company, we are seeking a talented and motivated Scientist to join our dynamic team and contribute to the advancement of our gene therapy programs. Contribute to the development and optimization of gene therapy manufacturing processes.
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Experience with QC techniques and technology of Cell and Gene Therapy products including: flow cytometry, cell-based assays (i.e., Potency);dPCR/qPCR; HPLC; CE-SDS or SDS-PAGE. The Associate Director, Quality Control (Viral Vector) is responsible for managing the Quality Control Viral Vector team and testing operations to support GMP Cell and Gene Therapy Manufacturing.
$133,550 - $163,228 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We leverage our proprietary high-throughput AAV engineering platform to create viral vectors with cell-type and tissue level specificity, overcoming many of the biological limitations of early gene therapy efforts.
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This includes some of the traditional flagship Biologics, but Peptides, Gene Therapy, and as a result of a recent acquisition, includes Cell Therapy as well. Leading development of bioassays and potency assay for Cell Therapy Products, Proteins, Peptides, and Gene Tx.
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Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. Reports to QC Manager, Chemistry.
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A cutting edge clinical stage biotech dedicated to the cell therapy space is looking for a Senior Scientist of Translational Research to join their team! Senior Scientist (Translational) - Cell Therapy.
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You will be part of a team focused on performing preclinical-stage studies that are essential in supporting our next-generation gene therapy research. Affinia Therapeutics is an innovative gene therapy company with a vision to create a paradigm shift by broadening the reach of gene therapy to prevalent diseases.
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Process Engineer 1 (Gene Therapy Program) The Gene Therapy Program (GTP) is entering a new era of unprecedented opportunity with great potential to reshape the face of medicine as we know it.
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Develop bioreactor-based cell culture processes for manufacturing of AAV-based gene therapy vectors across multiple preclinical programs. We are seeking an Upstream Process Development Associate to join a growing gene therapy company out of South San Francisco.
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A strong understanding of molecular biology techniques for analysis of gene therapy products: to include (but not limited to) PCR, Infectivity, Potency, and various ELISA methods. Function as an internal expert in RNA and molecular Biology test methods used for release and characterization of Gene Therapy products intended for human use.
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Familiar knowledge of GLP and GMP requirements as they pertain to protein and gene therapy process development and Quality Control (QC) testing is a plus. Leads the activities associated with the development and execution of methods relevant to protein and gene therapy products for analytical development in a Research and Development environment.
$125,700 - $182,250 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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We are situated in a city that is rapidly growing into the leading worldwide biotech hub for cell and gene therapy, and hence appropriately dubbed “Cellicon Valley”. The ideal candidate will have prior experience working with iPSCs or gene therapy or LNP-based delivery approaches.
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ElevateBio is looking for a Cell Therapy Manager, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Manager will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events.
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gene therapy jobs Title: qc scientist Company: Thermo Fisher Scientific
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