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Mirus, together with Gamma Biosciences, is establishing the future of science and medicine by developing products that enable researchers within the cell and gene therapy space. 2 years’ experience in the cell and gene therapy industry and/or biosciences tools industry.
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At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale.
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At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale.
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Extensively characterize compounds using various physical and chemical characterization techniques such gel permeation chromatography (GPC), dynamic light scattering (DLS), nuclear magnetic resonance spectroscopy (NMR), high performance liquid chromatography (HPLC), fluorescence, mass spectrometry (MS), Infra-red spectroscopy (FT-IR.
$75,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Company is a leading provider of research services for the Cell/Gene Therapy and Regenerative Medicine market. If you are looking to be exposed directly to the exciting Cell/Gene Therapy market in a fast-growing venture, this position is for you.
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Strong technical background in Molecular Biology, Biochemistry, Cell Biology or Cell and Gene Therapy required. Strong technical background in Molecular Biology, Biochemistry, Cell Biology or Cell and Gene Therapy required.
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Clear technical experience in design and operation of cell and gene therapy. 5 years in BioPharm/Cell and Gene Therapy Industry experience. Clear technical experience in design and operation of cell and gene therapy.
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Cell and Gene Therapy Department. Knowledgeable in several of the following areas: HPLC, UPLC, iCE, CGE, MS, ELISA, SDS-PAGE, Biopharmaceutical Testing, Karl Fischer, UV-Vis, FT-IR, TOC. Laboratory experience involving CE, HPLC, ELISA and compendia.
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Experience with Cell and Gene therapy product testing. Apply Quality Systems: Event and CAPA Management System, Document Management System, Learning Management System, Change Control System and new technologies.
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Scope The Sr Engineering Project Manager will deliver major projects on schedule and within budget across the organization. Direct cGMP related experience required for FDA / EMA regulated environments.
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At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. Our team of dedicated, forward-thinking associates share this goal by combining best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide.
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