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In-depth knowledge and specific understanding of analytical testing needed in drug discovery as it relates to DMPK.Understanding of GMP/GLP/GCP regulations with the ability to apply these practices daily.
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Oversee assay transfer to QC or at contract testing organizations used for release testing of viral vectors used as raw material or final product in GLP animal and GCP human clinical studies.
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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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Supports animal and human cadaver studies to help define clinically accurate use condition requirements for verification testing or to demonstrate that products meet requirements (GLP study.
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Who You Are: You will build a team of scientists to develop new peptide-based therapeutics in categories like GLP-1, GIP, PYY, Amylin, and Glucagon agonists. Your expertise in drug discovery, especially in peptides, will help us develop affordable next-generation GLP-1 drugs for all Americans.
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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. Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition.
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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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Lab experience and/or experience working within GLP, GCP or GMP Quality Assurance preferred but not required. In the Quality Assurance role, you will put your scientific education, experience and on-the-job training to work by performing protocol, raw data, and report audits for compliance with regulatory requirement (GLP, GCP & Part 11), SOPs, and protocol, reporting all findings from the audits and inspections to Study Directors, Principal Investigators, Test Site Management, Test Facility Management and Operational Management and scientific personnel.
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Assist with performing non-destructive testing to ensure quality and detect defects; methods include: Visual Inspection, Ultrasound Testing, and Magnetic Particle Testing. Assist Technicians setup and calibrate non-destructive testing (NDT) equipment.
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Can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment.
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This includes performing analytical testing under Current Good Manufacturing Practices (CGMP) production of cell and gene therapy products, immunologic monitoring of test samples, research, and development.
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The company offers integrated preclinical drug development services including cellular and animal disease model design and development, non-GLP and GLP efficacy, toxicity, biodistribution, and product release studies in a broad range of animal species.
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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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Required Skills : ETL Testing focused on Big Data, python automation, and working on Google Cloud Platform (GCP) Basic Qualification : QA testing, ETL testing, Python, and GCP. Additional Skills : QA testing, ETL testing, Python, and GCP.
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About Insourcing SolutionsCharles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment.
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glp testing jobs Title: associate Company: Aequor
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