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The successful candidate will work well in a highly collaborative team environment and possess expertise in flow cytometry, mammalian cell culture, and cell engineering. Evaluate target expression on engineered and endogenous cell lines using flow cytometry and molecular characterization.
$51 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As the head of Biologics Development, you are responsible for the end-to-end, cell vial to product vial, development of biologics manufacturing processes, which include antibody, conjugation, formulation and drug product.
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The Senior Manager, Cell Therapy Instrumentation will lead a product management team that is passionate about developing and driving a multi-generation product portfolio strategy to commercialize instrument solutions that support the development and manufacturing of cell therapies.
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Strong working knowledge of cGMP regulations and Regulatory Agency requirements applicable to biologics and cell therapy manufacturing. The Director, QC is a key member of the Quality Control Leadership Team responsible for the design, implementation, and continuous improvement of all processes/systems in support of the Quality Control testing program at the Bothell Cell Therapy manufacturing site.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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At Bristol Myers Squibb we are reimagining the future of cell therapy. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
$200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of cell engineering platforms, including transient transfection, generation of stable cell lines, and CRISPR. Perform routine cell culture maintenance and banking, working with both primary and cancer cells.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Hands-on cell culture experience includes operating both bench-top glass vessel, large-scale single-use bioreactor systems, and associated activities. Supporting the Upstream cell culture operations in our pilot-scale lab (up to 250L) to generate protein materials needed for cross-functional developments as well as GLP toxicology studies.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Their primary responsibilities will include engineering cell lines and performing flow-based assays to support antibody campaigns. Experience with FACS and single-cell cloning. Order constructs for overexpression and knockout cell line generation.
$50 an hourExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Proficiency in culturing/maintaining multiple cell lines under BSL2 conditions. Experience in multi-color flow cytometry. Basic molecular biology skills, including vector design, cloning, and PCR.
$51 an hourExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Experience with cell therapy or other biopharmaceutical manufacturing. The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration and validation in the Client Syncade Manufacturing Execution System.
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Within the MGT, this role will be primarily responsible for supporting the Upstream cell culture operations in our pilot-scale lab (up to 250L) to generate protein materials needed for cross-functional developments as well as GLP toxicology studies.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported the commercial launch of Lundbeck’s first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Ph. D. or M.S. in cell biology, molecular biology, biochemistry or related field with 8+ years of relevant experience (for Ph. D) or 12+ years relevant experience (for M.S) in biologics. Develop, optimize and qualify potency methods (including cell-based bioassay and ligand binding potency assays) that are intended for lot release, stability-testing, product characterization, reference standard qualification and comparability evaluation.
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In partnership with QC, serve as the Subject Matter Expert (SME) in the transfer of analytical methods from Lundbeck to GMP contract labs/contract manufacturing organizations (CMOs) Ability to translate the mechanism of action into a cell-based assay.
ExpandApply NowActive JobUpdated 2 days ago
manufacturing cell therapy jobs Company: Careerbuilder Us in Bothell, Peoria, Arizona
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