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Hands-on experience with wide range of cell and molecular biology techniques to characterize in vitro and ex vivo systems that include (but are not limited to) mammalian cell culture, plate-based cell assays, western blotting, qPCR, flow cytometry and ELISA.
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CGMP manufacturing experience, preferably cell/gene therapy, with experience in tech transfer, process validation, project management, and change management. We are seeking a highly motivated Executive Director of Operations who will be responsible for the launch, ramp-up, and oversight of cGMP Operations within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products.
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As an Electrochemical Cell Design Engineer, your mission will be to bring solutions to the design and manufacturing of components for RenewCO₂'s electrolysis cell, mechanical components & system designs.
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We seek a postdoctoral fellow to study how metabolism is differentially regulated throughout the cell cycle, and whether there are cell cycle phase-specific metabolic vulnerabilities that can be exploited in cancer.
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We are seeking an experienced and dynamic Associate Director to lead our in vivo CAR-T cell therapy program. This individual will report to the Executive Director in R&D. This position will play a pivotal role in shaping our in vivo CAR-T cell therapy program.
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Work with cell therapy products and associated assays (dPCR, qPCR, cell-based potency assays, proliferation assays, ELISA, flow cytometry assays, etc.) Prior experience with immune cell phenotyping by multicolor flow cytometry, dPCR, qPCR, cell-based potency and other cell therapy related assays is preferred.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
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Experience with implementation and optimization of a broad range of in vitro cell-based and molecular assays is critical (especially multi-color flow cytometry and cell culture). Successful candidates will have a very strong foundation in cell-based assays (flow cytometry, proliferation, cytotoxicity, cytokine release, etc) and some background in human T cell biology and/or other immune cell types.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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In addition to providing clinical care, our academic institution in collaboration with Robert Wood Johnson Medical School creates unique opportunities for physicians to engage in clinical and research programs, clinical trials, cancer chemoprevention, basic and clinical pharmacology, novel cell therapy constructs, and participation in a broad range of teaching initiatives.
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Ability to secure and/or maintain a CDL Class B with airbrake endorsement (for applicable CDL positions) BlueTriton is a certified CDL provider and can assist you with obtaining your Class B CDL.
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Other courses that would be helpful are: Microbiology, Organic Chemistry, Analytical Chemistry, Instrumentation Analysis, Molecular Biology, Cell Biology, Biochemistry. Other courses that would be helpful are: Microbiology, Organic Chemistry, Analytical Chemistry, Instrumentation Analysis, Molecular Biology, Cell Biology, Biochemistry.
$15.5 - $17 an hourTemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Leads the Cell Therapy manufacturing sites ecosystem as an IT manager with ownership of local products and works toward re-defining to a platform or standard product according to JJT strategy. Johnson & Johnson Innovative Medicine is recruiting a Technical Product Senior Manager CAR-T Manufacturing Systems to support the North America (NA) region for our Advanced and Cell Therapy Manufacturing business in Raritan, NJ.
$118,000 - $203,550 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The processing areas are PLC automated and controlled via HMI. Cell Culture operations contains major equipment such as bioreactors, centrifuges, and biosafety cabinets. BioServices encompasses Media Prep, Buffer Prep, and general equipment cleaning and preparation supporting both Cell Culture and Purification.
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To support further expansion, the Upstream Manufacturing Associate/Scientist will be responsible for executing mammalian cell culture processes and producing proteins for a wide range of mammalian based biosimilars.
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non cdl cell phone jobs Title: sales representative in Somerset, NJ
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