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Precigen is advancing an exciting pipeline of novel cell and gene therapy products and to further our efforts we are seeking an Executive Director, Medical Affairs who will be instrumental in creating and building the global medical affairs function at Precigen for our first commercial launch.
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Arcellx isa public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. Join us in our quest to reimagine cell therapy and destroy cancer.
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The CMC project manager (PM) in Oncology Cell Therapy Tech Ops (CTTO) will build project plans, coordinate delivery of CMC activities in line with project requirements, plan and monitor resources and expenses for product development and clinical manufacture.
$40 - $45 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Minimum 15 years' experience in process engineering, supporting the process development, scale-up and manufacture of cell therapy processes at a pharma, biotech or contract development and manufacturing organization (CDMO.
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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5 years of experience in mammalian cell line development, cell therapy workflow, cell therapy applications or any combination of education and experience. Product Specialist, Cell Therapy.
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Manages symptoms/toxicities/health abnormalities related to the intense high dose therapy, stem cell rescue and rehabilitation following rescue in collaboration with transplant physician and/ supervisor.
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Arcellx, Inc. ( is a clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. Biologics/Cell Therapy experience preferred.
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Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and Cell & Gene Therapy products.
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At Miltenyi Biotec, 3,000 employees worldwide develop pioneering solutions for biomedical science and the clinical application of cell therapies. For over 30 years, Miltenyi Biotec has provided innovative tools, instruments, and solutions that advance biomedical research and cellular therapy.
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Precigen is seeking a highly motivated and creative Senior Scientist, Adenovector Research and Development (level determined by candidate experience) with demonstrated experience in adenovectors for cell and gene therapy to support our research and development initiatives in our Germantown, MD office.
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Relevant experience in auto or allo cell therapy CMC project management. Experience in planning, managing, and executing functional and/or cross functional aspects of cell therapy product development is desired.
$50 - $57 an hourExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Bachelor's, Master's, PhD or equivalent industry experience in a relevant technical discipline such as Biochemistry, Cell Biology, Molecular Biology, Immunology or Chemical Engineering. Bachelor's, Master's, PhD or equivalent industry experience in a relevant technical discipline such as Biochemistry, Cell Biology, Molecular Biology, Immunology or Chemical Engineering.
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Experience working within CMC and tech transfer (e.g. analytical development and/or QC) for cell therapy products is strongly preferred. We are seeking a self-motivated, detail-oriented Senior Research Associate to join the Analytical Development (AD) team to support process development, stability, and characterization of autologous cell therapy products.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. As Gene Therapy Manufacturing Supervisor, you will play a critical role in helping to establish REGENXBIO's first internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability.
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cell therapy jobs in Gaithersburg, MD
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