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In addition to wet chemistry testing, candidate will perform some biology experiments such as ELISA, PCR and microbial growth plating. Other courses that would be helpful are: Microbiology, Organic Chemistry, Analytical Chemistry, Instrumentation Analysis, Molecular Biology, Cell Biology, Biochemistry.
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Perform and oversee a wide range of analytical tests, including but not, UV-Spectrophotometry, qPCR, ELISA, HPLC, Endotoxin, MicroBCA, Electrophoresis, and DNA Sequencing/Analysis. Experience working with HPLC, qPCR, ELISA and/or DNA Sequencing/Analysis.
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The position reports to the Sr. QC Manager, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer.
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Extensive experience in cellular and immune cell-based analytics and assay development including, but not limited to advanced multi-parameter flow-cytometry, cell labeling, mixed lymphocyte reactions, cell proliferation assays, cytotoxicity assays, cytokine release ELISA/MSD multiplex assays.
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In depth understanding and technical knowledge of the analytical methods such as UV absorbance, SDS-PAGE, HPLC, IEF, and ELISA performed under QC laboratory environment, and be familiar with all basic and some complex laboratory equipment/instrumentation.
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B-Development of ELISA assays. Development of ELISA assays. Molecular biology and protein purification, biochemistry. The Associate Scientist will be part of a highly collaborative team working towards obtaining new cattle vaccine licenses.
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A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays.
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Has familiarity with FDA guidelines for biosimilars, USP, GLP, cGMP, Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines, ICH guidelines, and SOPs. Stability sample management documentation, including adherence to test scheduling.
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Lead QC-Analytics initiatives including equipment qualification, method development, method validation, tech-transfer, protocol execution, process development and optimization support. Degree in Molecular Biology, Biochemistry, Microbiology or related scientific field.
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Experience in microbiological techniques, ELISA, PCR and cell-based analytics is preferred. The Principal Scientist is a senior scientific role whose primary responsibility is to lead program-specific method development activities for therapeutic proteins in our company's biologics portfolio, from the discovery interface through first product registration.
$149,400 - $235,100 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience With FACS, Immunofluorescence-based Assays, ELISA, PCR, and maintain awareness of competitive landscape in the cellular immuno-oncology space. new/enhanced knowledge regarding cellular immuno-oncology-based products, intermediates, starting.
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3+ years of experience in the field of immunotherapy, cell therapy, immunology or oncology. Cell therapy and immune-oncology experience is preferred. Knowledge of state-of-art allo-cell therapy and its applications.
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Knowledge of protein synthesis, purification, characterization (SDS-PAGE, Western Blots, Elisa, etc.) Support Regulatory CMC Cell Therapy group in the preparation of CMC Regulatory Strategy and submissions and interactions with Global Health Authorities.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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ELISA (HCP, proA) and binding potency assay. Must have current cellular/ molecular biology and immunoassay experience. Support of routine release/stability, in-process, and/or cell-line development testing.
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elisa job in Fanwood, NJ
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