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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.
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Experience should include technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership for cell therapy manufacturing and processing equipment, manufacturing support and technology transfer.
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The Portfolio Analyst for Cell Therapy Business Process Management (BPM Portfolio Analyst) works with the Project & Portfolio Management (PPM) team to manage the portfolio of projects and enhancements to enable CTDO late stage clinical and commercial operations.
$48 - $51Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking a highly motivated Vice President 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.
$300,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The ideal candidate will have: Bachelor's degree 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 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.
$54 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience and solid knowledge of Pharmacovigilance specificallyProficiency in one or more of these additional areas is a plus: CMC/Mfg., Clinical development and trial execution, Regulatory, Real-World Data and Real-World Evidence, Cell and Gene Therapy, Medical Device, IVD/CDxExperienced in understanding and interpreting regulatory guidelines and documents.
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This person will conduct cell-based tests using techniques such as western blotting, qPCR, flow cytometry and ELISA. They will also provide statistical analyses using Excel, GraphPad Prism and FlowJo. The ideal candidate for this position will possess a high attention to detail and strong communication skills.
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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.
$52 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The primary focus of the Senior Research Associate – Attributes role will be to build CAR/TCR T cell product and process understanding in support of early and late-stage CAR T with a particular focus on exploratory/investigational needs for mid-stage programs.
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A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy. We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong technical knowledge related to Cell Culture process and equipment (i.e. Bioreactors, wave reactors, media and harvest vessels, related analytical equipment, and process control software.
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This position is a member of the Cell Therapy Development and Operations (CTDO) organization, which supplies autologous and allogeneic cell therapies for first-in-human and pivotal clinical trials.
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Hands-on experience with various bioanalytical techniques including ELISA, qPCR and FACS and cell-based assays. The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
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Job Description: Assistant QC ScientistOnsite role, Warren NJWork Schedule: Mon - Fri, AM - :PM EST Purpose:The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products.
$40.82 - $42.82ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Prior cell therapy assay experience is highly preferred. Supporting cell therapy products and associated assays. Prior cell therapy assay experience is highly preferred. Role reports in the QC Manager in a fast paced, growing organization.
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cell job Title: retail in Bernards, NJ
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