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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.
$21 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Chemist II will support the Quality Control Laboratory in analytical testing in compliance with GMP and GLP requirements. Performs analytical testing pursuant to available qualified methods of analysis, including but not limited to: moisture analysis, tapped/bulk density, particle size via sieving method, UV-Vis spectrometry, FTIR spectrometry, TOC, HPLC and UPLC chromatography, dissolution, disintegration, weighing, etc.
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As a part of Clinical Trials Scientific Affairs, the Principal Scientist will support testing, method development and validation. Ensure all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP), Medicines and Healthcare Products Regulatory Agency (MHRA), Food and Drug Administration (FDA), International Organization for Standardization (ISO), etc.
$115,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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On the laboratory testing side, the SME will also be responsible for GMP testing of raw materials, in-process and finished products, stability sample testing, and non-routine sample analyses per established procedures and methodology, internal laboratory audits, maintaining cGMP/GLP compliance (audit readiness) within the QC chemistry laboratories.
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Knowledge and understanding of clinical drug development strategic planning of clinical research, ICF, ICH GCP, GLP, In Vitro Diagnostic Regulation (IVDR) 2017/746, General Data Protection Regulation (GDPR), and clinical laboratory specimen handling.
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The ideal candidate should possess a strong background in chemistry, have a thorough understanding of cGMP, GLP, GDP guidelines, and be proficient in utilizing analytical instruments such as FTIR, HPLC, and ICP. Additionally, the Lab Chemist will collaborate closely with third-party laboratories, manage sample submissions, and generate Certificates of Analysis (COAs) to meet industry standards and regulations.
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American Testing Laboratories a Tentamus North America company is on the prowl for a S ENIOR ANALYTICAL CHEMIST to join our San Diego , CA Team! Implement and adhere to quality management systems, including Good Laboratory Practices (GLP) and ISO standards.
$75,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Inspect and perform complex chemical analyses on raw materials, in-process samples, and finished goods in accordance with cGMP/GLP standard operating procedures. Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required.
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Support on-going GLP programs by being a study director, as needed, and supporting the GLP coordinator as a back-up, as needed. The Formulation Scientist reports into the Associate Director of Product Development and will be responsible for developing novel formulations and delivery systems to support new product introductions specifically for GSS customers serving the turfgrass, ornamental, and structural pest management industries.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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As the Analytical Laboratory Supervisor, you hold a pivotal position in conducting essential testing for raw materials, finished bulk products, and third-party product releases. Ensure that the QC laboratory adheres to company policies, SOPs, cGMP, GLP regulations, and FDA regulations.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Founded in 1981, TETRA Technologies, Inc. ( NYSE: TTI ) is a geographically diversified industrial and oil and gas products and services company, focused on completion fluids, calcium chloride, water management solutions, frac flowback and production well testing services.
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Job Details INTRODUCTION:JOB TITLE: Testing Coordinator OFFICIAL TITLE: Proctor DEPARTMENT: Disability Services APPOINTMENT PERCENTAGE (FTE):. Hourly, Full-time Academic Year JOB DUTIES Reporting to the Director of Disability Services (DS), the Testing Coordinator assists in maintaining an accessible and inclusive testing environment for students with disabilities.
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Prior experience working in a CLIA, ISO, GLP or cGMP environment. The Lab Tech will contribute to the creation and distribution of certified laboratory dried blood spot materials in support of regulatory compliance and accreditation for testing: quality control materials and proficiency testing materials.
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The Senior Analyst / Scientist will also support the gene therapy program pipeline including but not limited to technical transfer, method qualification, validation, verification, routine GMP testing of AAV vector analytical methods (HPLC, AUC, UV, CE-SDS, compendia methods and other methods as needed) for lot release and stability.
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Perform non-destructive testing techniques at industrial facilities, including ultrasonic, magnetic particle, liquid penetrant, and visual inspections. Nova Data Testing is currently looking for hard-working and dependable experts as Non-Destructive Testing Technicians to support our projects in the South East and the New England regions.
$22 - $30 an hourFull-timeExpandApply NowActive JobUpdated Today
glp testing jobs Title: associate Company: Aequor
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