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AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API.
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For the Senior Validation, Engineer level: Working knowledge of target systems, including computerized information systems, manufacturing control systems (e.g., PLC, BMS, DCS, and SCADA systems), and laboratory automation systems (e.g., robotic systems, chromatography networks, data acquisition systems.
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Furthermore, the staff scientist assists in the management of resource allocations, and may manage day-to-day activities in the laboratory, such as purchasing, oversight of laboratory animals, radioactivity, and biosafety issues.
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Molecular Laboratory (CLIA and CAP accredited) performing Next Generation Sequencing. Molecular Genetics and Genomics or Laboratory Genetics and Genomics. High-Complexity Laboratory Director (HCLD) certification in Molecular Diagnostic; OR.
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Active ABMGG board certification with 5 years of clinical and/or laboratory genetics experience as an attending and/or in an academic/commercial lab setting. Active ABMGG board certification with a minimum of 3 years of clinical and/or laboratory genetics experience as an attending and/or in an academic/commercial lab setting.
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The RF test engineer will test and calibrate classified RF systems at the Naval Research Laboratory in Washington DC and at other locations. The RF test engineer will capture and evaluate test signals using spectrum analyzers, RF power meters, and other standard laboratory equipment.
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American Society for Clinical Pathology or American Medical Technologists Board certification consistent with scope of responsibility to include: Medical Lab Scientist/Medical Technologist (MLS/MT), Medical Lab Technician (MLT), Histotechnician (HT), Histotechnologist (HTL), BB, C, H, M, CT), or Laboratory Technologist Certification (HEW.
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Research associate, RA, infectious disease, flu, influenza, life sciences, preclinical, cro, contract research organization, in vivo, research, research study, animal studies, mammalian cell, bsl 2, glp, sop, sops, standard operating procedures, lab, laboratory, vaccine, research and development, elisa, immunology, immunoassay, pipetting, centrifugation.
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Certification/Licensure: AALAS certification at the Assistant Laboratory Animal Technician level (ALAT) required. We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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Perform detailed RF test procedures using spectrum analyzers and other standard laboratory test equipment. This position will be full time on-site at the Naval Research Laboratory in Washington DC and will be in a classified environment.
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Charles River also provides a suite of products and services to support our clients clinical laboratory testing needs and manufacturing activities. Additional duties may include ensuring appropriate inventory levels of expendable supplies; assisting with ordering, receipt, and stocking of supply inventories; in addition to organizing, unpacking, and rotating stock, plus taking part in laboratory housekeeping.
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Analyzes and monitors legislation and federal policy related to maternal health, drug shortages, laboratory testing, workforce, and physician resilience and well-being (including administrative burdens associated with hematology practice such as prior authorization issues), consistent with Society policy, political opportunity, and the goals of Society leaders.
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Perform, with technical independence, basic and advanced laboratory procedures such as Plasmodium falciparum tissue culture, genetic manipulation, nucleic acid extraction, PCR, qPCR, CRISPR-targeting design, and next-generation RNA and DNA sequence analysis.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. Coordinate daily operations and lead on the floor manufacturing employees to complete production activities safely and compliantly in accordance with OSHA and cGMP guidelines.
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Conduct clinical research studies involving administration of investigational products according to the principles of current Good Clinical Practices (cGCP), Good Laboratory Practices (cGLP), and Good Manufacturing Practices (cGMP) and in accordance with all relevant host nation, US Federal, Department of Defense (DoD) and Army regulations and policies.
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cgmp laboratory jobs in Bethesda, MD
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