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Mosaic teams provide comprehensive, end-to-end discovery services, including program assessment and strategy development; program management; antibody discovery and optimization; protein production, purification, and characterization; protein engineering; biochemical and cellular assay development; formulation, stability and developability studies; bioanalytical (PK and PD) assay development; and candidate-validating pharmacology.
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And cell-based assay development. Ph. D. with 2+ years FAS or customer-facing experience in cell biology, immunology, molecular biology, biochemistry, or related field. Ph. D. with 2+ years FAS or customer-facing experience in cell biology, immunology, molecular biology, biochemistry, or related field.
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You will be responsible for conducting daily laboratory tasks and preparing consumables for the assay development team. Correlia Biosystems is looking for exceptional new team members to contribute to our manufacturing and assay development team.
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Experience in areas of technology development pertinent to impurities and potency assay development, including but not limited to assay automation and miniaturization, FcgR effector function assay development, large-scale cell banking, image and flow cytometry, and monitoring and characterization of diverse HCP’s.
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We are seeking a highly motivated and talented scientist with background in cellular and molecular biology and assay development to join the Biotherapeutics and Genetic Medicine organization to support in vitro pharmacology work related to Genetic medicine research on AAV.
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A PhD in Analytical Chemistry, Biochemistry, Molecular Biology, or related field with at least two years of relevant post-graduate experience in a CMC setting driving routine assay workflows.
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Basic knowledge of assay development. Minimum of 2 years of biochemistry, analytical chemistry (quantitative analysis) or molecular biology laboratory experience. Minimum of 2 years of biochemistry, analytical chemistry (quantitative analysis) or molecular biology laboratory experience.
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This role will contribute to the growth of Belharra's research portfolio through the production of high value target proteins to enable biophysics, high-throughput screening, and general assay development.
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Ability to work with external CROs and guide the development and validation of bioanalytical assays Requirements Required Qualifications PhD in Biochemistry, molecular biology or cell biology with technical expertise in molecular and immune assay development and minimum 6 years industry experience in biopharma development with a primary focus on the development and validation of bioanalytical methods.
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Requirements: BSc or MSc in Pharmaceutics, Chemistry, Biophysics or Biochemistry preferred, with >10 - >7 years of industrial experience; or PhD in Pharmaceutics, Chemistry, Biophysics or Biochemistry with >3 years of relevant experience.
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Support customers in experimental design and assay development activities. Masters degree or higher in chemistry, biochemistry, biophysics or a similar degree with emphasis on chemistry and biology; a Ph. D. degree is preferred.
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Troubleshoot issues and complaints related to biochemistry, assay or experimental design, software, instruments, or user's technical skill. Proficient with molecular biology and NGS assay technology.
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The QC Analyst II will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies.
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We are seeking an experienced Senior Manager, Field Applications - APAC who will lead/manage Field Application Scientists (FAS) in achieving both short-term and long-term company goals and the placement and development of designated 'strategically-important' products, services, and capabilities.
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The focus of the work will be on structure determination by cryo-EM (specimen preparation, data collection, data processing and analysis) and assay development for complementing our structural analyses.
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