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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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Minimum 1+ years speech therapy experience required.
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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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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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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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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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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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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.
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The LVN / LPT provides direct client care including medications and basic medical intervention and education, following standard nursing practices. Graduation from an accredited school of licensed vocational nursing or psychiatric technology required.
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Stanford Hospital & Clinics is known worldwide for advanced patient care provided by its physicians and staff, particularly for the treatment of rare, complex disorders in areas such as cardiac care, cancer treatment, neurology, neurosurgery, orthopedics We consider excellence in surgery for lung cancer to be at the core of the mission of the Thoracic Surgery service at Stanford.
$2,878.23 a monthFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. This role is in the Technical Operations (Tech-Ops) organization within Analytical Development and Operations (ADO), based at our headquarters in Foster City, CA. The group is responsible for CMC analytical activities related to the development of Gilead's small molecule drug substances and drug products.
$138,820 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The VP of Drug Safety & Pharmacovigilance will interface with vendors, external experts, business partners, investigators, and government agencies. The VP of Drug Safety and Pharmacovigilance will provide the leadership and management for the infrastructure of the Drug Safety and Pharmacovigilance department across both clinical development and commercial products for the company.
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nursing we hiring drug jobs Title: maintenance technician Company: Legend Senior Living in Redwood City, CA
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