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Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP.
Full-timeExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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He/She will also support testing required for drug substance and drug product process development, characterization of impurities, and other activities associated with GLP Toxicology and cGMP Clinical Trial materials.
$90,000 - $130,000ExpandUpdated 2 days ago - UpvoteDownvoteShare Job
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This position will provide quality oversight to ensure that cGMP, GLP, and other regulations and policies are followed. This position will provide quality oversight to ensure that cGMP, GLP, and other regulations and policies are followed.
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Applies GMP/GLP in all areas of responsibility, as appropriate. Applies GMP/GLP in all areas of responsibility, as appropriate. Documentation of glass wash cycle issues in glasswash logbooks. Picks up, rinses with appropriate solvent, stores properly, cleans pipettes, performs siliconizing) in all glass wash areas.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Chemistry, HPLC, pipetting, lc-ms, glp, wet chemistry. chemistry, HPLC, pipetting, lc-ms, glp, wet chemistry. B.S. Chemistry, Biochemistry, Biology, Microbiology or related Life Science Degree. Run biological extractions on biological samples like urine, blood, plasma and etc.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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CGMP, Good Documentation Practices (GDP) or Good Laboratory Practices (GLP) knowledge experience. The Quality Control (QC) team is responsible for testing products, raw materials and the manufacturing environment to ensure the Safety, Quality, Identity, Purity and Potency produced by the Catalent Madison Biologics facility.
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Arrowhead Pharmaceuticals is seeking a Scientist/Senior Scientist to join the Bioanalytical group within the Clinical Pharmacology Department.
$120,000 - $140,000Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The position will be introduced to food, dietary supplements, and Micro samples for entry. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies.
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Demonstrated understanding of working in a high-complexity laboratory or similar environment with professional working knowledge of HIPAA, GLP, GDP, and laboratory terminology and equipment. Demonstrated use of applicable software, such Epic or laboratory information system (LIS.
$85,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Essential Duties and Responsibilities: Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Manages the daily activities of the hazardous waste storage and disposal per regulations outlined in the Code of Federal Regulations, 40 CFR (EPA) and Wisconsin Department of Natural Resources.
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