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AcuraStem seeks individuals with deep knowledge of iPSC neurodegenerative disease models, high-content imaging, and assay development. Applies analytical techniques, including the design of experiments and statistical process control, to diagnose assay performance issues.
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Design and complete development experiments, research/source reagents, develop assay workflow, and participate in analytical activities related to both upstream and downstream processes.
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Experience across overall assay development with immunoassay experience highly preferred. Senior Research Associate of Assay Development to support and execute assay development working with a team of analytical scientists, engineers, data scientists, researchers, and more as they develop products with the aim of early detection of cancer through liquid biopsy samples.
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The Senior Associate, Analytical Development will be responsible for the execution of routine testing, including but not limited to flow cytometry assay, cell-based cytotoxicity assay, or PCR-based assay, to characterize or release engineered TCR-T cell drug product.
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Experience with protein characterization, electrophoresis, chromatography, aseptic techniques, cell culture, LAL and assay. Previous experience in either HPLC/CE or Potency/ELISA assay methodologies is required.
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Work closely with a bioinformatics team on the design, development and implementation of proteomics experiments to support assay and platform development. Provide scientific thought leadership in the development and implementation of strategic and tactical plans aligned with overall business objectives.
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You will closely collaborate with our reagent and assay development groups as well as system integration to define and document process maps, workflows, work instructions and QC methods, design and execute DOE, participate or lead Critical Parameter Management activities as well as lead troubleshooting and sustaining activities.
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Assist in establishing and optimizing in-house ddPCR assay development. Combined with additional technologies under development, Link will advance a suite of exciting internal therapeutic programs while exploring opportunities for value creation with strategic partners.
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Demonstrated knowledge and experience in "core" laboratory techniques (ELISA, Cell culture and Cell-based assay, PCR, Flow cytometry, etc.) ImmPACT-Bio is seeking a QC Sr. Associate in the Quality Control organization to support the development, implementation, and maintenance of the raw material program for Clinical and future Commercial Manufacturing of the new GMP cell therapy production facility located in West Hills, CA. This individual will work closely with cross-functional teams (e.g., Manufacturing, Quality Assurance, Supply Chain, etc.
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Establishes and executes development project plans (e.g., process and assay development, assay qualification, support tech transfer of processes) from cGMP manufacturing and assays to quality control.
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Interface cross-functionally with early development, assay laboratories, in-vitro diagnostics, and biomarker representatives to drive omics-based biomarker development. The Clinical Biomarkers & Diagnostics (CBD) department at Company is looking for a highly motivated Computational Biologist with expertise in causal machine learning models and the development of predictive signatures from multi-omics and multi-modal biomarker data to enable clinical biomarker discovery and development.
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Skilled at FACS, molecular biology, mammalian cell culture and assay development. Skilled at FACS, molecular biology, mammalian cell culture and assay development. Demonstrated skill in operating a binocular phase microscope, personal computer, spectrophotometer, tissue culture equipment, autoclave, and balance.
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Create and execute project plans for process and assay development and support the transfer of processes to cGMP manufacturing and quality control. As the Associate Director of Process Development, the individual will be responsible for creating protocols and methods for the production of various cell and gene therapy products, procuring the necessary equipment and components for cGMP production, making adjustments to the process and reagents to meet cGMP requirements, facilitating technology transfers, and developing assays for product characterization.
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Work with bacteriophages and associated analytical assays such as plaque assay, PCR, ELISA, gel electrophoresis and etc. Armata is committed to advancing phage with drug development expertise that spans bench to clinic including in-house phage-specific cGMP manufacturing.
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We are looking for a talented individual to join our dynamic Drug Product Development team within the Company’s Biologics CMC organization, where we drive the maintenance and evolution of both clinical and commercial products and programs.
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assay development jobs in Los Angeles, CA
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