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Work in collaboration with the Analytical Development team to ensure timely transition of lab developed methods to GLP ready state. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes.
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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.
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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. 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.
$187,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Oversee the development and implementation of test plans test cases and test scripts for REST / API Service Testing and Webservices (SOAP-UI). The ideal candidate will have extensive experience in AWS Cloud Generative AI IBM InfoSphere MDM Siebel MRM REST / API Service Testing Infa MDM Testing Webservices - SOAP Snowflake Informatica MDM Informatica MDM SAAS IBM MDM Testing Informatica Testing Python and Automation Testing.
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The Study Technician provides primary care to the animals in the small and large animal toxicology department and performs routine invasive and non-invasive technical procedures on studies allocated to the team while ensuring that procedures are conducted according to protocol, SOP requirements, Good Laboratory Practice (GLP) and United States Department of Agriculture (USDA) regulations and the guidelines The Guide for the Care and Use of Laboratory Animals.
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Has direct development and oversight responsibility for planning, design, and implementation of the System Testing Program, including scheduling resources, track access, availability of equipment, training, witnessing tests, and oversight and management of project scope.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As a Study Director, you’ll be the single point of control for assigned studies, responsible for the interpretation, analysis, documentation, and reporting of study results for both GLP and non-GLP studies.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Support establishing LC-MS GLP/GCLP regulated capability and facilitate method development, validation, and sample analysis to support clinical and preclinical programs. Track record with analytical development with deep expertise with bioanalytical LC-MS platform to support PK/TK, efficacy in clinical and preclinical toxicology studies.
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As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries.
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Collecting and reviewing data in accordance with the Good Laboratory Practice Regulations (GLP) and standard operating procedures. Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies.
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Authorize maintenance and testing activities to ensure equipment status is maintained. Power Plant Watch Engineer, Engineering Watch Supervisor, Reactor Operator, Engineering Officer of the Watch, Propulsion Plant Watch Supervisor.
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The initial license trainee will engage in a combination of classroom instruction, simulator training, and on-the-job experience, to acquire the essential skill and knowledge to meet the qualification for a Senior Reactor Operator License holder.
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It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Directs and manages the care of patients in the Outpatient Endocrinology Testing department at LVH-Cedar Crest. Collaborates with inpatient pharmacy to ensure proper medications are available on testing days.
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Additional certifications or coursework in Laboratory Management, Quality Assurance, or Good Laboratory Practice (GLP) compliance are considered an asset. Experience in a GLP compliant laboratory an assetFamiliarity with laboratory safety standards, compliance regulations, and best practices.
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glp testing jobs Title: analytical development chemist
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