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Extensive experience in late-phase drug product development and commercial development with CMC regulatory filings for the US (NDA), Europe (MAA), Japan, and China. Thorough understanding and working experience of pharmaceutical drug products concerning GMP, quality systems, ICH guidelines, FDA, EMA, and associated regulatory requirements.
$118 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Our Client's global life sciences practice, one of the largest in the U.S., is seeking a regulatory counsel with at least 10+ years of industry experience in drug/biologics development to join our FDA regulatory group.
$435,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The mammographer is required to be completely familiar with, and adhere to, all U.S. Food and Drug Administration (FDA) guidelines regulating the practice of mammography, radiation safety, and quality assurance requirements.
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Juvena’s approach integrates proteomics, transcriptomics and imaging with phenotypic human in vitro disease model screening and extensive preclinical validation to mine stem cell secretomes as a rich source of new medicines for chronic and rare diseases.
InternExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Excitement about synthetic biology and AI-driven small molecule drug discovery. We are looking for a Chemistry Lead to build out internal chemistry capabilities, including medicinal chemistry, chemical synthesis, and analytical chemistry.
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As a mammographer, also called a mammography technologist, you'll take X-ray images of patients' breasts for screening and diagnosis. We have plenty of local opportunities as well. As a mammographer, also called a mammography technologist, you'll take X-ray images of patients' breasts for screening and diagnosis.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The current vacancy would be responsible for supporting IHSS consumers who do not have caregiver resources, in hiring a homecare provider from the Public Authority Registry and helping the client and provider establish a successful working relationship.
$116,085 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage manufacturing activities for viral vector and cell therapy, including cGMP aseptic qualification, in support of manufacturing and formulation of viral vectors as drug substance and of cell therapeutics as drug products.
$254,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Given the firms nexus to companies with next-generation products and innovative biotechnologies, we commonly help clients with novel technologies and therapeutics and develop FDA regulatory strategies for seeking marketing authorizations.
$435,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Employment with GAT Airline Ground Support is contingent upon a clear driving record, 10-year criminal History records check, and drug screen as required. GAT Airline Ground Support is a drug-free workplace and conducts a random drug test.
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Title: Licensed Vocational Nurse (LVN)/Licensed Psychiatric Technician (LPT) Job Duties: The Licensed Vocational Nurse (LVN)/Licensed Psychiatric Technician (LPT) is a member of the interdisciplinary team that supports the people we serve in their recovery journey.
$43.6 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking an experienced professional with excellent communication skills to join the real world evidence team at Gilead Sciences. Experience in drug development is a plus. We are seeking an experienced professional with excellent communication skills to join the real world evidence team at Gilead Sciences.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Duties:Provide expert legal advice and guidance on FDA regulatory requirements and compliance for drug, biologics, cellular, and gene therapy products. Firm Type: Law Firm, Experience: 10 Years, A law firm based in Palo Alto is seeking a highly experienced Senior FDA Drug/Biologics Regulation Counsel to provide comprehensive legal support in FDA regulatory matters pertaining to drug and biologics development.
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Demonstrates technical understanding of bioanalytical workflows, including sample analysis strategies, instrumentation and general laboratory operations with familiarity of pharmacokinetics in drug development.
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The candidate must have extensive knowledge and practical experience in analyzing and characterizing Biological Drug Products (proteins, polysaccharide conjugates, vaccines) using a number of techniques, including HPLC, CE, spectrophotometric techniques, light scattering and particle sizing techniques.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago
nursing we hiring drug screening jobs Title: technician Company: Legend Senior Living in Redwood City, CA
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