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The Viral Vector Commercial Network Manufacturing Science and Technology (MS&T) group within CTTO plays a critical role in technology transfers, process validation, CMC life cycle management, technical oversight of external manufacturing partners, process engineering and establishing manufacturing standards to enable a robust and scalable global cell therapy manufacturing network.
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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. Optimizing the manufacturing process and determining root cause of manufacturing deviations are critical to ensure uninterrupted vector supply for BMS' clinical and commercial cell therapy assets.
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We are seeking a Cell Therapy Medical Communications Director with a deep understanding of the relevant disease states, medical education, scientific customer experience and communication within Cell Therapy Medical.
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Lead the development of vector control strategy within a cross-functional team in support of clinical engineered T cell programs. If you want to challenge yourself, accelerate your career, and give new hope to patients, theres no better place than here with our Cell Therapy team.
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At Bristol Myers Squibb we are reimagining the future of Cell Therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of Cell Therapy as we strive to put more patients on the path to a cure.
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We are looking for a motivated Sr Manager, Contracts Negotiation – Cell Site Leasing to support T-Mobile’s network siting and construction process. Certain positions in Customer Care are eligible for monthly bonuses based on individual and/or team performance, while Retail and Business Sales roles are eligible for monthly or quarterly sales incentives.
$142,600 - $202,600 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Position Summary:The Associate Director Supplier Relationship Manager (SRM) is accountable for overall relationship management and operational oversight of one or more contract manufacturing organizations (CMOs) used in the manufacture of cell therapy materials and products.
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Thorough general knowledge of bioassay test methods (e.g. Elisa, Flow cytometry, qPCR, cell culture) Support Bioanalytical laboratory by execution of in-process and release testing on batches including, but not limited to, flow cytometry, IFNg potency, qPCR, cell count and viability, sterility, and endotoxin.
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Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions. Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.
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Familiarity with Pressure Transducers and/or Load Cell Manufacturing Duties and Responsibilities: Develop and improve welding processes, including Laser, Electron Beam, Rolling Seam, and TIG. Collaborate with cross-functional teams to optimize machining processes, specifically CNC lathe, CNC mill, and MasterCam. Conduct research and implement application and test methods for load cell/sensor specifications.
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This exciting role serves as a technical associate expert to support analytical testing and implementation of novel analytical methodologies for our CAR-T cell therapy products. Understanding of the basic scientific principles underpinning the analytical methods such as flow cytometry, PCR, ELISA, cell-based assays.
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Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology. Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology.
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In oncology, hematology, cell therapy, immunology, Neuroscience, and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change.
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The purpose of the Facility and Reliability Engineer is to development and implement a Reliability Centered Maintenance (RCM) strategy to support Summit West Cell Therapy Operations and to maintain a qualified and compliant facility operation status.
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BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry, preferably with 1-3 years CMC regulatory experience. Experience with CMC regulatory documents (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents.
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cell phone jobs Title: retail sales associate in East Hanover, NJ
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