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The Technical Writer and Document Specialist (TW/DS) will sit within the Cell Therapy Development (CTD) Development Operations and Services (DO&S) Portfolio Management Office (PMO.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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Executes experiments and analyzes data from flow cytometry analytical assays with limited supervision, as part of the Cell Therapy Analytical Development (CTAD) team. Flow cytometry assay development experience is preferred.
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The Cell Therapy Attribute Sciences department is seeking a Senior Research Associate to support the development of gene engineered T cell products. Attribute Sciences is responsible for developing and executing mechanism of action and characterization studies to support the development of gene-engineered T cell therapies.
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with Client policies, standards, procedures, and Global cGMP requirements.
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The Technical Project Manager (PM) will be a key member of the Cell Therapy Development (CTD) Development Operations & Services (DO&S) Portfolio Management Office. 5+ years’ experience in bio tech/life sciences project management; cell Therapy experience preferred.
$75 - $85 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Excellent knowledge of Logistics and IT processes ideally with experience in the design, development, testing, deployment of SAP ERP system.
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Collaborate closely with CMC functional areas, including process development, analytical development, quality, and regulatory, to support project objectives. Lead and coordinate Drug Product Process Development and related CMC sub-teams to ensure alignment with overall project goals and timelines.
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Execution of formulation and process development, tech transfer, scale-up, and alternate raw material supplier qualification batches. The candidate will work on a variety of processes, supporting the BMS portfolio from early development through post commercial launch.
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They will coordinate activities within the Technology Center, supporting colleagues from Drug Product Development, Clinical Supply Operations, and Manufacturing Science & Technology. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow.
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This position will be supporting both the Biologics and Cell and Gene Therapy sites throughout the Catalent network for clinical and commercial applications. CDMO knowledge, Biologics and Cell Gene Therapy experience highly preferred.
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Familiarity/experience with end-to-end CMC drug development. The project(s) will be technical in nature and will support an individual product program or the development portfolio as a whole, with a particular focus on Drug Product Process Development support and alliance management.
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The primary purpose of this position will be to support daily lab operations and to manage lab equipment and inventory within Cell Therapy Development. At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science.
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Experience in using CMMS software Blue Mountain Regulatory Asset Management (BMRAM). Schedule and escort vendors to perform duties on jobsite per company policy. Knowledge of laboratory instrumentation pipettes, balances, centrifuges, flow cytometers and other equipment.
$23 - $24.77 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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cell therapy development jobs in New Brunswick, NJ
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