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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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QPS, LLC is an innovative and dynamic Contract Research Organization (CRO) that has been assisting pharmaceutical, biotechnology, and medical device companies with their drug development efforts by providing a full range of GLP-compliant bioanalysis, DMPK, and protein/genomic biomarker services since 1995.
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Three (3) years experience working in a regulatory environment or position (GLP, GCP or GMP), a plus. Ability to understand and comply with GLP regulations, principles and Guidance Documents.
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Contract Research Organization (CRO) that has been assisting pharmaceutical, biotechnology, and medical device companies with their drug development efforts by providing a full range of GLP-compliant bioanalysis, DMPK, and protein/genomic biomarker services since 1995.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience with in vivo preclinical ADME studies and understanding of clearance route and mechanism, and the role of metabolism/catabolism is essential. MIST, metabolite DDI, reactive metabolites), radiolabel positioning and interpretation of results; sample extraction; LC/MS and radiometric metabolite profiling and characterization of metabolites (small molecules, peptides, oligonucleotides, siRNA) from complex biological matrices; interpretation of HRMS data; structural elucidation of metabolites.
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Animal handling, Animal science, Husbandry, glp, tail vein, histology, Ascp, HTL. The candidate will be a member of the Developmental and Reproductive Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
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Humane care to laboratory rodents; careful handling/restraint of animals. Evaluation of developmental/reproductive toxicity endpoints across multiple generations. Data collection manually and electronically (experience with Provantis Integrated Preclinical Software a plus.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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General Toxicology Associate Scientist will be a member of the General Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection from rodents, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
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The candidate will be a member of the General Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection from rodents, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
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Title: General Toxicology Associate Scientist. Blood (tail vein) and urine collection, clinical observations, and other in-life study functions. B.S. degree in animal science, biology or related science field with 2 years of relevant experience or an equivalent combination of education and work experience.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Understand and comply with the Quality System Regulation and OSHA safety requirements; Requires the basic knowledge of GMP regulations (GLP and GDP); Knowledge of FDA, ISO, and IVDD. Experience with automated immunoassay analyzers and/or ELISA and chemiluminescent technology is a plus.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities. The successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline: Ph. D. degree o Recent graduates must have with direct experience on LC-MS/MS analysis o If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience Understanding of experimental design and planning, and data collection and analysis software.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Blood (tail vein) and urin collection, clinical observations, and other in-life study functions. Communicating effectively with Study Directors, peers, supervisors, and attending veterinarian. Body Weight, Food Consumption, holding for eye exams, other measurements and collection of biological samples as needed.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Associates or BS in Medical Technology, Biology, Chemistry, Biochemistry. Supports testing on clinical analyzers to provide assistance for production support and complaint investigation which is critical to ensure the supply chain requirements.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Familiar with GMP, GLP, and GDP processes. Completes manufacturing related testing/processes on analytical instruments such as Titrator, ICP, and Spectrophotometer and pH meter. Computer skills: MS Office programs, SAP, LIMS, and/or Siemens Clinical testing software.
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