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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.
$26 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Description: Maintain and manage inventory of GLP and Clinical bioanalytical samples and critical reagents. Responsibilities: Maintain and manage inventory of GLP and Clinical bioanalytical samples and critical reagents.
$28 - $29 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Maintain records and test results following good laboratory practices (GLP) At least six months related laboratory experience preferably performing biologics purification steps. Experience with chromatography or membrane operations such as tangential flow filtration is preferred.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Keywords: Chemistry, Chemist, HPLC, GC, Gas Chromatography, Mass Spectrometry, Karl Fischer, cGMP, GMP, GLP, LIMS, Laboratory Technician, Quality Control, Pharmaceutical, SCM, pH, Dissolution, Disintegration, Compendial.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Nonclinical Drug Safety department in West Point, PA is seeking a Toxicologist to conduct and/or monitor toxicity studies (GLP and non-GLP) as a Study Director or Study Monitor and to potentially serve as a departmental representative on a product development team.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Lab Manager is the in-house expert on analytical methodologies, equipment, product and residue chemistry and Good Laboratory Practice (GLP) and associated certifications. Maintain GLP and ISO certifications at the SHIP facility in support of in-house regulatory studies.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Attention to detail, strong knowledge of GCP, GLP, and regulatory requirements, and ability to build partnerships will be essential in achieving operational excellence and ensuring clinical trials are performed in accordance with study protocols and in compliance with all applicable regulatory requirements.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Perform laboratory work to GLP/GMP quality standard to support the development of biopharmaceutical products. Experience working in a GMP/GLP laboratory environment. Perform laboratory work to GLP/GMP quality standard to support the development of biopharmaceutical products.
$60,000 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Related experience could entail construction, plant engineer, or facility management in a GMP or GLP regulated environment (pharma, biotech, med device, diagnostics). Related experience could entail construction, plant engineer, or facility management in a GMP or GLP regulated environment (pharma, biotech, med device, diagnostics.
Full-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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At least six months of laboratory experience in upstream bioprocessing (e.g. bioreactor operations, mammalian cell culture in plates). Perform lab-scale upstream processing of vaccine products and process intermediates.
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Strong knowledge and hands-on experience working with quality management systems, standards, and regulations relevant to the industry, such as Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP.
$32 an hourExpandUpdated 18 days ago - UpvoteDownvoteShare Job
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Participate with the research team when conducting in vivo small animal studies. Experience working with cell/tissue culture. Basic laboratory skills including proficiency with micro pipetting, preparation and dilution of standard solutions, reading scientific literature, aseptic technique, and operation/maintenance of standard biological instruments.
$60,000 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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The Compliance Specialist for Bioanalytical Data and Lab Systems will play a critical role in ensuring compliance with policies, quality standards, workflow procedures, and regulatory and accreditation requirements.
$34.75 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Quality Compliance Specialist for Bioanalytical Data and Lab Systems will play a critical role in ensuring compliance with policies, quality standards, workflow procedures, and regulatory and accreditation requirements.
Full-timeExpandUpdated 17 days ago - UpvoteDownvoteShare Job
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Conform to Standard Operating Procedures (SOPs) and Good Laboratory Practice Regulations (GLP). About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
$21 an hourTemporaryExpandUpdated 1 month ago
glp job in Horsham, PA
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