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Demonstrated hands-on experience in assay development, especially for SEC, icIEF, CE-SDS, HIC, and residual-free drug analysis, is desired Experience in 2D-LC method development is a plus Experience in protein structural elucidation and peak identification using high-resolution mass spectrometry is a plus Experience in interfacing with CDMO/CTL for clinical or commercial biological products development is a plus Experience in method transfer and GMP qualification/validation is a plus.
$125,000 - $176,500 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversight and review of drug safety operations practices. Ensure case reports are appropriately scheduled in Argus based on regulatory reporting matrix in conjunction with Drug Safety submissions.
$210,000 - $297,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical and biologics services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Design and implement bench-scale experiments (1mL - 3L) utilizing bioinformatics tools for strain characterization purposes and bioprocess development; experience with data analysis and hypothesis generation for transcriptomics and proteomics experiments.
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Experience in ELISA assay development, cell culture, gene expression with RT-PCR and/or enzyme kinetics is desirable. Experience in ELISA assay development, cell culture, gene expression with RT-PCR and/or enzyme kinetics is desirable.
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We work with governments, civil agencies, foundations, universities, and private companies around the globe to drive better information about our oceans and seas—from sailing into the eye of a category 4 hurricane to obtain new data about how storms intensify collecting new CO2 data in hard-to-reach areas, and counting fish biomass to inform sustainable fishery management, to mapping the ocean floor and reducing illegal fishing and drug trafficking.
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Ripcord Business Development Representatives are the tip of the spear producing and driving business for Ripcord. Ripcord customers include global enterprises such as Coca-Cola, IRS, Allianz Insurance, and MUFG. We're based in the Bay Area, California and are backed by the world's leading investors including Kleiner Perkins, Google Ventures, Lux Capital, Icon Ventures, Silicon Valley Bank, Apple co-founder Steve Wozniak and more.
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Our Small Molecule Drug Substance Development and Manufacturing team has an opportunity for Scientist position to support our small molecule drug development pipeline. Work in a team of Arcus scientists and partner contract development and manufacturing organization teams to develop efficient manufacturing processes for small molecule drug substance preparation under GMP. The projects may encompass clinical stage candidates through commercial launch.
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The Scientist 2/Senior Scientist in Analytical Development will assume a pivotal role within GeneFab’s Technical Development department, executing against and supporting oversight of the analytical functions (method development, qualification, routine testing, and new technology evaluation) that are integral to the successful development and manufacturing of cell and gene therapy products for new or existing clients.
$115,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Rusfertide, a mimetic of the natural hormone hepcidin, is the Company's lead drug candidate currently in a global Phase 3 development program. Synthesis of peptides in a highly efficient manner by either solution phase or manual/automated solid phase synthesis to support peptide drug discovery programs.
$120,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Saildrone works with governments, civil agencies, foundations, universities, and private companies around the globe to drive better information about our oceans and seas—from sailing into the eye of a category 4 hurricane to obtain new data about how storms intensify, collecting new CO2 data in hard-to-reach areas, and counting fish biomass to inform sustainable fishery management, to mapping the ocean floor and reducing illegal fishing and drug trafficking.
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Rite-Hite is an Equal Opportunity/Affirmative Action employer offering a drug free workplace for our customers and employees. The incumbent will work in concert with the District Service Manager and Installation Manager in developing and implementing strategies that will maximize synergies between functions and promote teamwork.
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Experience with a range of assay development in next-generation sequencing techniques, including both library preparation and data analysis. Track record of methods development and innovation.
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Gene editing/gene therapy drug development program experience is a requirement. Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing technologies by developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by Design platform for CRISPR-based genetic medicine.
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Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred.
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drug development jobs Company: Genoskin in Hayward, CA
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