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Pacific BioLabs is an independent CRO offering cGMP/GLP testing services in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology. Pacific BioLabs has immediate openings for the position of Life Science Client Account Manager I. The Life Science Client Account Manager ensures our clients enjoy the optimal customer experience supporting Pacific BioLabs' mission to be "The Service Leader in Life Science Testing.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Performs and directs assays according to, and in compliance with Good Laboratory Practice (GLP), current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Will perform analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. Familiarity of regulatory guidelines as well as GMP/GDP/GLP practices.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Performs Study Director functions as outlined by FDA Good Laboratory Practices (21 CFR Part 58) for GLP Studies, as well as serves as a technical leader in ensuring proper execution of additional microbiology testing (testing of bioburden, sterility, endotoxin, biological indicators, etc.
TemporaryExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The QAU will support the comparable GMP production activities related to GLP toxicology lot production and technical transfer activities as it relates to clinical batch release testing conducted at GTP to support the clinical CMO. The QAU will also provide Quality Assurance support to the research-based portion of the GTP, in terms of SOP management, training, document management and archiving, and audit support.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Primary Responsibilities Include:Conduct protocol and protocol amendment reviews, in-study inspections, and data and report audits for nonclinical, method validation, and clinical sample testing studies for compliance to applicable regulations (GLP, GCP), methods, and SOPs. Perform facility inspections to assure management that the facilities, equipment, personnel, methods, practices, records, and controls are in conformance with GLP regulations.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Chemical testing using established methods for OTC drugs, cosmetics, dietary supplements, and Rx drug. A strong understanding of cGMP/GLP requirements and QA procedures for an analytical laboratory.
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The Senior Bioanalysis Scientist I is responsible for assay development, validation, and sample testing to support non-clinical and clinical studies for a fast-growing Exelixis pipeline of novel biotherapeutics.
$113,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Experience performing immunoassay testing in a GLP laboratory. An emphasis on Good Laboratory Practice (GLP) compliance for all work and documentation is required. Accurately perform immunoassays (ADA/NAb) following well defined guidelines as per their respective SOPs and checklists in a GLP laboratory.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience in GMP pharmaceutical product testing and knowledge of GDP and GLP requirements. Supervise lab personnel regarding all quality testing, including raw materials, post-pack production, and in-process checks.
ExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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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. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The GMP Microbiology Lab Analyst will perform microbiological assays, related to bioburden testing, utility monitoring, raw material, and finished product testing in accordance with cGMP/FDA regulations as they apply to the pharmaceutical industry.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Technical sales, radio frequency (Must have knowledge of RF products) mechanical design, mechanical engineering, automated testing procedures, Sales, business development, complex mechanism design, Sales engineering, Sales support, engineering design, engineering support.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Ensure the timely completion of testing, tasks, and assignments while identifying and implementing improvements to optimize workflow, throughput, quality of work, and compliance. Schedule and balance testing and other tasks for optimization.
ExpandApply NowActive JobUpdated 10 days ago
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