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Solid background in virology, antiviral drug discovery, molecular biology, cell biology, and immunology, with practical working knowledge of viral-host interactions and viral disease.
$149,200 - $248,600 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Perform or assist in routine procedures in bacterial culture; molecular biology (e.g., DNA and RNA purification, PCR); clone and produce recombinant polypeptides; and immunological assays (e.g., ELISA.
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Independent scientists with a strong command of neuroscience-based in vivo and ex-vivo techniques, metabolism, molecular biology and biochemistry to contribute to target discovery, validation and preclinical development for novel therapeutics are encouraged to apply.
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Broad experience in biochemistry, flow cytometry, molecular biology, in vitro and ex-vivo assays are essential. The candidate will be responsible for guiding and implementing rigorous ground-breaking in vivo mechanistic studies for target discovery, validation, and novel therapeutic development.
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We are need experience in Oncology, Immuno-Oncology or Immune-Inflammatory disease drug development. Collaborate with internal Regeneron laboratories (e.g. Discovery Research, Molecular Profiling, Regeneron Genetics Center, DNA core, BioAnalysis, etc.
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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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Support bioassay testing for raw materials, drug substance and drug product, including generation of testing data to support clinical studies. 0-2 years of direct experience in QC Molecular testing and Cell Biology (e.g. qPCR, sequencing, potency, mammalian, and bacterial cell culture.
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You will apply your full stack software engineering skills in modern web user interface design and development, analytics pipelines, and database technologies to digitize drug discovery processes that bring breakthrough medicines to patients.
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Must have demonstrated success commercializing IVD products including immunoassay, molecular and POC through FDA, Health Canada, and the EU as well as ROW. It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.
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This individual will have direct contact with our Hematology/Oncology Physicians, Infectious Disease Physicians, and their patients. Shift: Mon-Fri 84P, 95P, 117P, alternation w/eDescription:Under the general direction of the Director of Pharmacy Services, the Registered Oncology Pharmacist provides comprehensive pharmaceutical care and work with our Infusion Center, Hematology Oncology Unit and Oncology Physician Practice nursing staff.
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Be a professional Design Consultant through the use of the La-Z-Boy In-Home Design program and drive top line sales through the use of selling principles including approach, rapport building, needs discovery, customized portfolio presentations, answering objections, closing, follow-up, after sale service, and continuing contact with all previous and potential customers.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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What Aptar Pharma Is Looking For: Tend to utilities & process equipment; serve as the first responder for the following plant systems – Heating Ventilation Air Conditioning (HVAC) Chillers High-Pressure Boilers Compressed Air Purified Water Generation Mixing Skids Cleanrooms Maintenance Terminology & Principles Pharmaceutical Terminology & Principles Neptune Computerized Maintenance Management System (CMMS) ETQ Reliance Food & Drug Administration (FDA) Good Manufacturing Practices (GMP.
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Microbiology - Performs Bacteriology, Parasitology, Virology, Mycology, Mycobacteriology, Susceptibilities, and Molecular testing under supervision by a CLS or technical Supervisor. Ensures the accuracy and quality of all results from pre-analytic, analytic, and post-analytic phases of testing.
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A thorough understanding of the drug development process from pre-IND through registration and post-registration and a broad understanding of functional areas of drug development, including (preclinical, regulatory, pharmacology, translational medicine, pharmacovigilance, data sciences (data management, biostatistics, programming), and clinical operations is require.
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LOTTE BIOLOGICS entered the biologics CDMO business after acquiring Bristol Myers Squibbs Syracuse biologics drug substance manufacturing site, as of January 1, 2023! Leverage drug substance downstream purification process knowledge to design, execute, and analyze scale-down chromatography and filtration laboratory studies for process development, process characterization, and process validation.
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disease molecular drug discovery jobs Title: post fellow Company: Emory University in Tarrytown, NY
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