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HemaCare, a Charles River company, is a global leader and trusted brand in the customization of human-derived biological products and services for biomedical research, drug discovery, and cell and gene therapy development.
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You will have demonstrated experience, leadership, and independence with QC functions associated with the GMP production and testing of cell/gene therapy products or biologics in both clinical and/or commercial settings.
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Here at Kelonia Therapeutics, we aren’t just a preclinical company; we’re trailblazers in viral engineering, pushing the boundaries of in vivo lentiviral gene and cell therapy. At Kelonia, we've gathered a group of pioneers in cell and gene therapy to lead our journey, with extraordinary scientific founders at the helm, providing the cutting-edge technology that sets us apart.
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Minimum of 7-10 years of experience in strategic sourcing, procurement, or supply chain management, with a focus on CDMO for Cell and Gene therapy or biologic in the pharmaceutical or biotechnology industry.
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The Commercial Supply Chain Manager will lead the overall management of Cell and Gene Therapy supply chain activities required to support slot management including capacity planning and slot scheduling.
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We became a wholly-owned, independently operated, subsidiary of Bayer AG in late 2020 as a cornerstone of its newly formed Cell & Gene Therapy (CGT) platform. Asklepios BioPharmaceutical, Inc. (AskBio) is a leading, clinical-stage gene therapy company founded in 2001 based on the work of adeno-associated virus (AAV) gene therapy visionary and pioneer, Jude Samulski, PhD. Since that time, our commitment to developing life-saving medicines that can potentially cure genetic diseases has never wavered.
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She / he is responsible for partnering with Strategic Sourcing & Procurement to ensure that the right network partners are identified at the right time and managed to assure robust supply of BMS cell and gene therapy products.
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Principal Scientist, Gene Therapy Analytical Development page is loaded Principal Scientist, Gene Therapy Analytical Development Apply remote type On-Site locations US CA San Diego time type Full time posted on Posted 3 Days Ago job requisition id R4430 Who We Are: At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values.
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Clinical or industry experience in sickle cell disease, thalassemia, gene therapy, bone marrow transplant, or rare diseases (blood disorders). bluebird bio is seeking an accomplished and adaptable Director Medical Affairs to join the medical affairs team, focused on our gene therapy programs for Sickle Cell, Beta Thalassemia, and CALD. You will be joining a passionate and committed flock, flying closely with medical birds as well as the cross functional teams.
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Applicants should have a PhD degree or an MD with post-graduate scientific training, and at least three years of research experience in relevant areas such as Molecular Biology, RNA biology, Biochemistry, animal modeling, Immunology, Gene Therapy, Cell Therapy, Bioengineering, Neuromuscular Biology, Cell Biology, and Virology.
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Develop and exhibit extensive and comprehensive knowledge of the research and biotech/ life- science (including bioproduction, gene therapy, and cell therapy) markets to enable effective customer engagement.
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REGENXBIO is seeking a highly motivated Upstream Manufacturing contractor to establish REGENXBIO's 1 internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability.
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Working knowledge of gene-based therapy approaches (gene regulation, RNA medicine, gene therapy, gene editing, and/or gene silencing) not required but desirable.
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Contractors) and analytical techniques to develop a comprehensive understanding of our gene-modified cell therapy products from preclinical development through commercial launch. Maintain awareness of the current state of the field (literature, regulatory expectations, and competitive surveillance), and contribute to the broader cell and gene therapy industry and academic ecosystem through publications and conference presentations.
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The Sr. Principal Formulation Scientist - Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and execution of compliant manufacturing of gene therapy drug product and drug substance.
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