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We are seeking a highly motivated, collaborative, and innovative Associate Director of GLP/GcLP Compliance within the Clinical Assay, Supplies and Logistics (CASL) team who will be responsible for performing and overseeing QC activities within the Clinical Biomarker Laboratories (Immuno-Assays BioAnalytics, Virus Neutralization, Biobank, Flow Cytometry, Spectrometry, etc.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Skills: Quality control, SOP, FDA, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) skills: Quality control, SOP, FDA, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Familiarity with GDP, GMP, Good Laboratory Practices (GLP), FDA, and ISO. Assembly, cleanroom, packaging, Production, Hand tool, Inventory, Inspection, Quality assurance, Packing, manual dexterity.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Familiarity with Pharmaceutical Quality regulations (GLP, GCP, GMP) Familiarity with Pharmaceutical Quality regulations (GLP, GCP, GMP) Hybrid schedule with one day per week on-site. Experience (want some lab and data generation experience) after school 3.
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Provide holistic evaluation of patient, review labs, and if appropriate, prescribe different weight loss medications (primarily GLP-1’s such as Wegovy, Trulicity, or Ozempic) Experience prescribing GLP-1s or strong interest in learning.
Starting at $112 an hourRemoteExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Collaborate with Quality teams to ensure compliance with regulatory standards, including but not limited to GMP, GLP, and GCP, as applicable. The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure.
$160,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The VP, Quality will have end-to-end Quality responsibilities inclusive of leading GLP, GCP, GVP and GMP functions. Collaborates with internal functions and aligns goals and objectives for pre-clinical to commercial phase programs and products, ensuring cGMP, GCP, GVP and GLP compliance and realization of other value-added guidelines and best practices.
$315,000 - $320,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The CIC is an independent unit housed within the VMC that provides infrastructure and technical support for veterinary preclinical and clinical studies in a GLP- and GCP-compliant environment. The CIC team includes the center Director (a medical oncologist), a DVM Research Manager, five research technicians and a veterinary technician assistant.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Experience performing immunoassay testing in a GLP laboratory. An emphasis on Good Laboratory Practice (GLP) compliance for all work and documentation is required. Responsibilities Accurately perform immunoassays (ADA/NAb) following well defined guidelines as per their respective SOPs and checklists in a GLP laboratory.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The PMG Graduate Leadership Program (GLP) is a hands-on leadership development program for recent graduates of bachelor’s or master’s programs who are interested in working on data-driven digital and technology solutions and creating an impact for leading brands such as Apple, GAP and Sephora.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Strong knowledge of the biological impact of drug product materials and familiarity with GLP and ISO regulations. Position Title: Pharmacologist/Toxicologist, Nonclinical Operations & Risk Assessment.
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Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., FDA, EMEA, GCP, GLP, GMP, QSR, etc.) Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., FDA, EMEA, GCP, GLP, GMP, QSR, etc.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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This person must comply with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Laboratory Safety and any regulatory requirements. Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements.
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Proven and complete understanding of R&D processes and scientific concepts working in a GxP environment specifically GLP, GCP, GDP, and GMP. Proven and complete understanding of R&D processes and scientific concepts working in a GxP environment specifically GLP, GCP, GDP, and GMP.
$184,240 - $276,360 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago
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