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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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Good understanding of relevant areas such as biostatistics, regulatory, clinical pharmacology, pre-clinical toxicology, pharmacogenomics and biomarker-based approaches. Good understanding of relevant areas such as biostatistics, regulatory, clinical pharmacology, pre-clinical toxicology, pharmacogenomics and biomarker-based approaches.
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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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Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP.
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Knowledge of GLP requirements and understanding of current industry trends and regulatory expectations associated with bioanalytical science. Previous work experience in regulated industry environment and a solid understanding of current GLP standards NOTICE FOR INTERNAL APPLICANTS In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
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The successful candidate will be actively involved in method development and project support in collaboration with data science teams, computational and experimental protein scientists, computational and medicinal chemists, project biologists, toxicology and pharmacokinetics and IT colleagues.
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Extensive experience managing preclinical studies through external CROs, with proven ability to oversee outsourced toxicology and ADME work in both non-GLP and GLP environments. Manage relationships with CROs, ensuring the successful outsourcing, execution, and quality control of toxicology studies in both non-GLP and GLP settings.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Work collaboratively with functional partners including Clinical Development, Biostatistics, Discovery, Translational Medicine, CMC, Toxicology, DMPK, Clinical Operations and Regulatory to deliver on project and corporate objectives.
$246,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Lead and manage the Pharmacology and Toxicology unit, setting strategic vision and fostering talent development. Board certified by the American Board of Toxicology (ABT) and/or American College of Veterinary Pathologists (ACVP), European College of Veterinary Pathology (ECVP) or Japanese College of Veterinary Pathology (JCVP.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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NMS Labs has developed an extensive menu of more than 2,500 Clinical and Forensic toxicology tests to support clients in healthcare, public health and public safety fields. Initiate, coordinate and enforce optimal warehouse security, operational policies, and procedures, maintaining standards of health, safety, and hygiene.
$97,000 a yearFull-timeExpandApply NowActive JobUpdated 7 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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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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Experience in collaborations with medicinal chemistry, analytical, biology, toxicology, clinical pharmacology, Quality Assurance, Regulatory CMC and CMC development departments. Responsible for timely deliveries of drug substance to support IND/IMPD enabling toxicology studies as well as manufacture of phase-appropriate cGMP drug substance.
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Responsibilities cover the entire R&D GxP spectrum – GLP, GCP, GCLP, GVP and GMP as well as medical device and combination products regulations. Quality oversight is provided for toxicology studies, clinical development, clinical supply manufacture and packaging and medical device development.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Bachelor’s or Master’s degree in Environmental Science, Biology, Toxicology, Public Health, or related life science discipline or related field, from an accredited curriculum. Assist clients in stakeholder management activities related to contaminant toxicology, vapor intrusion, and risk assessment.
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toxicology glp jobs in Gwynedd Valley, PA
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