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Regulatory, CMC, drug development, pharmaceutical, biotech, chemical engineering, GMP, IND, IMPD/CTA, NDA, MAA. 10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs and small molecules.
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Experience in late phase drug product development and commercial development with CMC regulatory filings for US (NDA), Europe (MAA), Japan, and China. Lead and/or support activities for pharmaceutical profiling, phase appropriate formulation development, and drug product manufacturing of the new chemical entities of RevMed during preclinical assessment and throughout clinical development phases.
$135,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Director, Assay Development leads product technology development activities including IVD development, automation of NGS protocols, and in-house reagent manufacturing.
$200Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role reports to the Director of Product Management on the FC Mobile team. Lead product strategy and prioritization discussions. Role Overview As a Lead Product Manager you will drive business performance goals by driving actionable product insights and recommendations to shape the identity of FC Mobile.
$125,300 - $204,700 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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PhD in a discipline related to pharmaceutical drug discovery and development, e.g., Biochemistry, Chemistry, Pharmacology, Physiology, Cell Biology, Molecular Biology or Genetics. Minimum of 5 years of experience in the biopharmaceutical industry or related fields (life sciences VC, life science technology transfer, consulting) with a preference for additional hands-on experience working on drug discovery projects and also with small life science companies, venture capital firms or in the external innovation deal making space.
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We are seeking a highly motivated, creative, and collaborative individual with a background in immunology and strong interest in investigating novel approaches to achieve drug-free remission or cure of HIV infection.
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Strengthen internal gene therapy CMC capability and serve as regulatory subject matter expert and influential leader within the R&D organization to contribute to drug development at Adverum for its development programs.
$250Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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EInfochips , an Arrow company (Fortune #109), is a leading global provider of product engineering and semiconductor design services. Please visit for our portfolio of product engineering services across various industries & verticals.
$84,700 - $131,300 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.
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Reporting to the SVP, Product Strategy & Commercialization, the Vice President, Global Program Team Leader (PTL) will be responsible for leading the cross-functional strategy team for one or more development candidates.
$246,000 - $339,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In this role you will work with the ADAS Cloud,Data, Perception, SIL/HIL, Vehicle integrations & Vehicle Cloud teams, Product Management, and other Technology Partners to leverage best practices and reference architectures highlighting AWS Cloud Platform and Data/Dev/ML Ops practices.
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Author/review and/or coach team members to author CMC regulatory sections of IND/INDa. Contribute to regulatory strategies and support associated agency interactions and product-related inspections.
$191,335 - $247,610ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking a highly motivated, creative, and collaborative individual with a background in immunology and strong interest in investigating Client approaches to achieve drug-free remission or cure of HIV infection.
$40 - $46.67 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This is a remote role and reports into the Director of Product, Prenatal. This groundbreaking technology is integral to our product offerings, including one of our flagship products, Unity Complete, the only non-invasive prenatal screen capable of assessing fetal risk for both common recessive conditions and aneuploidies from a single maternal blood sample.
$150,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Senior Director, CMC Regulatory Affairs for Biologics is responsible for leading a matrix team of professionals, who work with a specific product in Gilead’s global portfolio of biological products in CMC Regulatory Affairs.
$237,660 - $307,560 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
product drug jobs Title: development director Company: Omeros in Belmont, CA
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