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Established capability to design, conduct, optimize and execute on novel biochemical and cell-based assay development efforts in the lab supporting HTS and project deliverables. As a research associate in assay development you will develop, optimize, and execute novel enzymatic and cell-based assays in high-throughput screens using conventional approaches and robotics.
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Experience in cell culture and/or assay development is a plus. Hands experience on molecular biology, biochemistry, and cell biology techniques, such as molecular cloning, cell culture, DNA/RNA transfection, virus transduction, RNA isolation, real-time PCR, immunoblot, ELISA, MSD multiplex assay, cell viability assay, enzyme activity assay, etc.
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Working in a team setting, the Research Scientist II will be involved in Research and Development projects serving as a technical lead or a subject matter expert in translating research ideas and concepts into the product development pipeline towards development of diagnostic assay products.
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This position will support product development, including activities such as assay design, prototype optimization, design lock, verification, validation, and design transfer. For over 50 years, we have been partnering with healthcare and life science laboratories, manufacturers, and suppliers across the globe to co-create and provide biological control materials, assay services and consulting for microbiology, molecular diagnostics, and virology.
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The Molecular Assay Development team is seeking an accomplished (Senior) Scientist to join our team within the Cellular Therapy Analytical Development (CTAD) organization. The (Senior) Scientist will have extensive hands-on experience in assay development; possess excellent communication skills; and be able to work with cross-functional teams in order to effectively transfer analytical methods, as wells as maintain and troubleshoot existing methods.
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We are seeking an In vitro Assay Development Postdoctoral fellow to develop and execute strategies for analytical biomarker assay development in non-invasively collected samples to support existing work.
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Late phase clinical testing); lead the statistical activities in assay development, qualification, validation and testing to ensure the science, quality and compliance. External ; lead the stats contents when applicable in assay development, qualification, validation and testing to ensure the science, quality and compliance at CRO. Responsible for regulatory response and medical journal submissions when applicable.
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PhD with 2+ years of industry experience in molecular assay development, or. This position is responsible for the technology platform screening, development, qualification, and transfer of molecular biology-based analytical methods; as well as the life-cycle management of these methods.
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Pcr,elisa,assay,quality assurance,Quality control,cGMP,Cell Therapy,Flow Cytometry. pcr, elisa, assay, quality assurance, Quality control, cGMP, Cell Therapy, Flow Cytometry. Collaborates with other Functional Areas (Analytical Development, Materials Sciences and Technology.
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Status: Full Time (Regular) Primary Location: Company Office (Downtown Detroit) Secondary Location: Wayne State University Research Laboratory (Detroit) Overview Responsible for program management, assay development, clinical studies and talent development/management for R&D and laboratory functions.
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Ph. D. with expertise in complex molecular and genomics assays and relevant work experience in a biomarker or assay development group within a CRO, CMO, and/or Core facility; OR. With expertise spanning virology, immunology, and genomics, our team develops, scales, and commercializes complex assay workflows to support our biopharma partners from basic research through clinical trials.
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PhD with 2+ years of industry experience in molecular assay development, or MS/MA in Molecular Biology or similar with 5+ years of related experience, or BS/BA with 10+ years of related experience.
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In this position, you will provide technical and scientific oversight to the Genomic Services team and drive the validation and execution of innovative molecular biology and genomics assay services for biopharma and large academic clients.
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The Precision Medicne Pathology group within Precision Medicine supports projects from discovery through CDx assay development. The candidate is expected to design and execute novel tissue-based assay development experiments independently to enhance our biomarker research.
$78Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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ELISA assay development. Document experiments, results, and conclusions in electronic laboratory notebook; present work at group and department meetings; contribute to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publications.
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