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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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HistoWiz has over 1,000 paying customers globally from top academic institutions (e.g. MSKCC, Harvard, Stanford, HHMI) and pharmaceutical companies (e.g. CRISPR, Johnson & Johnson, Regeneron). In-depth knowledge and experience with GLP and/or GCP regulations and industry standards (EPA, OECD, FDA, EU guidance.
$120,000 - $150,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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The candidate is also expected to support outsourcing efforts for designing, monitoring, execution and reporting of the nonclinical toxicology studies, have experience in managing regulatory-compliant toxicology studies in a CRO or biotechnology/pharmaceutical company, and have demonstrated understanding of GLP compliance and the relevant ICH & FDA guidance documents.
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Comprehensive knowledge of GLP regulations, including previous GLP experience in pharmaceutical or biotechnology industry or equivalent GXP transferable experience. Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Job Segment: Biochemistry, Genetics, Biotech, Pharmaceutical, Science, Research. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
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Function independently as a study director in the direction and execution of assigned studies in compliance with GLP or other applicable regulations for the conduct of nonclinical and clinical research.
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Master’s degree in Biotechnology, Regulatory Science, Pharmaceutics or Pharmaceutical Science or Industrial Pharmacy (or its foreign equivalent); plus 6+ years of quality assurance experience within the pharmaceutical drug development industry as a Quality Assurance Manager, Lead, Specialist or Associate.
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Research Scientist, Pharmaceutical, Quantitative Analyst, Laboratory, Science, Research, Data. Characterize biotherapeutics by developing biosensor assays to quantitate antibody-target binding (e.g. kinetics, affinities) with high-throughput screens on various biosensor platforms.
$111,000 - $122,500ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
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Eight (8) years of experience in pharmaceutical drug safety/pharmacovigilance case processing including branded and generic products and all case types (spontaneous, clinical trial and litigation.
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Experience in GMP pharmaceutical product testing and knowledge of GDP and GLP requirements. Must have hands-on experience working on laboratory equipment like FTIR, HPLC, GC, AA, or ICP-MS.
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Bachelor's degree in Pharmaceutical Science, Chemical Engineering, Food Science, Chemistry, or a related scientific discipline. Theyre seeking a talented Senior Formulation Scientist to join our dynamic team and drive innovation in the Over the Counter (OTC) pharmaceutical and supplement markets.
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Strong knowledge of regulatory requirements and guidelines (e.g., cGMP, GLP, ICH) governing pharmaceutical manufacturing and testing. Overview : The QA/QC Analyst at AstraZeneca is likely responsible for ensuring the quality and compliance of products and processes within the company's pharmaceutical manufacturing or research facilities.
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Familiarity with cGMP, Good Laboratory Practices (GLP), and project management principles. The Senior Formulation Scientist will play a pivotal role in designing and developing novel confectionary-based OTC drug and supplement products.
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