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The successful candidate should have strong expertise in immuno-oncology and will be focused on focus on the development of fit-for-purpose CMC assays using flow cytometry and cell-based immunoassays, to characterize engineered TCR-T cell drug substance and drug product.
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Proficiency with diverse bioanalytical assays, including but not limited to ddPCR, qPCR, MSD, ELISA and flow cytometry. Proficiency with diverse bioanalytical assays, including but not limited to ddPCR, qPCR, MSD, ELISA and flow cytometry.
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Knowledge of general lab assays is required (e.g., Cell culture, ELISA, Flow Cytometry, Molecular Biology), but experience is preferred. Knowledge of general lab assays is required (e.g., Cell culture, ELISA, Flow Cytometry, Molecular Biology), but experience is preferred.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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In addition, this individual will conduct some routine characterization testing, using various laboratory methods (e.g., ELISA, Molecular Biology) Conduct some laboratory testing (e.g., ELISA, Molecular Biology.
$30 - $35 an hourExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Analytical Development, Analytical Testing and Logistics team at Kite Pharma is recruiting a Research Associate, to join our team. Cryopreserve cell therapy samples from clinical trials and development programs.
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Perform hands-on laboratory testing utilizing various analytical techniques including ddPCR, flow cytometry, cell counting, and cytotoxicity assays in support of cGMP clinical manufacturing. Perform statistical and analytical analysis of experiments as appropriate to ensure analytical assay trending and control; contribute to data packages for regulatory agencies, presentations, and publications.
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Preferred qualifications: Familiar with techniques such as multi-color flow cytometry and/or mass cytometry, sterile technique for cell culture with BSL-2+ practices, ELISA, qRT-PCR, and sterile technique for bacterial culture.
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Draft/revise SOPs and work instructions for sample management activities. Prior biological sample management experience, is a plus. Support sample management for routine in-process testing. Experience with Microsoft Word and Excel is essential, and knowledge in statistical programs (e.g., JMP) and languages (e.g., R and Python), is a plus.
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Flow cytometry, immunological characterization, and other similar tecchnical knowledge. Talentry is looking for a Process Development Scientist for a Biotech company in the West Valley area of Los Angeles in the Cell Therapy field.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Position is responsible for conducting Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
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Conduct Quality Control analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
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Performs protein electrophoresisi, EIA, IFA, coagulation, and flow cytometry testing. Performs protein electrophoresisi, EIA, IFA, coagulation, and flow cytometry testing. The Clinical Laboratory Scientist I (CLS I) in the Special Testing Laboratory is an entry level position that functions under the direction of senior technical personnel.
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MOST IMPORTANT PART: Conduct Quality Control analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
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Conduct routine QC testing for in-process and final release of drug products utilizing methodologies such as flow cytometry, PCR, and Cell based assays. Conduct routine QC testing for in-process and final release of drug products utilizing methodologies such as flow cytometry, PCR, and Cell based assays.
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Job Title : Quality Control Research Associate. All of previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software.
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cytometry job in Santa Monica, CA
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