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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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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.
$250Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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. Manage the hazardous waste (Resource Conservation and Recovery Act - RCRA) and medical waste disposal function including waste profiling, permitting, manifesting, and record keeping and reporting.
$75,000 - $80,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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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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.
$44 - $48 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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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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.
$20ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of laws, regulations, policies and guidelines that govern animal research, research conduct principles (GLP) and current methodology of laboratory animal medicine and management is important.
$155,000 - $185,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
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Proven track record of drug discovery, development and manufacture with extensive CMC and GLP/GMP knowledge and experiences. Coordinate activities with QA/QC and Management for development of tox and GLP batches.
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Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities. Good knowledge and application of GLP with the ability to train technical personnel. Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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In the Animal Care Technician II role, you will work with our research animals to ensure they are well cared for, including: In this role you will monitor daily animal health and welfare while performing daily animal health observations utilizing an assigned tablet device.
$21.8 - $26.7ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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What You Need: Degree in toxicology, pharmacology, chemistry or other related scientific field, with the following minimum previous experience working in the pharmaceutical/medical device industry in GLP/GMP environments: MS degree with 10+ years of relevant experience PhD with 8+ years of relevant experience Proven experience with the conduct and execution of GLP nonclinical safety (toxicology) and toxicological risk assessment on Extractable & Leachable is highly preferred.
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Maintain proper laboratory notebooks (follow GDP/GLP/cGMP) and prepare ARD/QC reports where applicable. Required Knowledge, Skills and Abilities Advanced knowledge in the pharmaceutical industry with advanced instrumentation skills, including HPLC, UV-Vis, UPLC, ICP/MS and USP dissolution apparatus 1, 2, 3, 4, and 7.
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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). Experience with X-Ray, CT, and MRI image processing software (i.e.,Mimics, 3-Matic, Amira, and 3D Slicer) preferred.
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glp job Title: associate Company: Aequor
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