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Using its unique drug discovery pipeline comprised of Artificial Intelligence, virtual screening, molecular docking, high throughput multi-omics sequencing, and human derived induced pluripotent stem cell technologies (hiPSCs), Greenstone Biosciences aims to develop novel drug therapeutics to achieve precision medicine and precision health.
$150ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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Forms cross-functional alliances with Small Molecule Drug Substance Development, Small Molecule Drug Product Development, CMC Regulatory Affairs, Quality Control and Manufacturing Operations by providing SMEs to these functions and project teams.
$221,170 - $286,220 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director of CMC Analytical Development's responsibilities will be:Create and put into place CMC analytical strategies to assist with drug development and regulatory submissions. Strong knowledge of regulatory requirements and guidelines for drug development and analysis.
$200,000 - $245,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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 Today - UpvoteDownvoteShare Job
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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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This position requires a comprehensive knowledge of SAS and CDISC standards, project and resource management, regulatory filing experience, and a broad understanding of the pharmaceutical drug development process.
$200ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Eurest services maintains a drug-free workplace. The Chief Facilities Engineer is responsible for providing assistance in the oversight of business activities, strategic planning and development, and program administration.
$150ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Broad understanding of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies, distribution across multiple regions.
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Lead purification process development and transfer to internal and contract manufacturing facilities to produce GMP and non GMP drug substances on time and with high success rate. Ph. D. in Chemical Engineering, Biochemistry, or related fields with 10+ years’ experience OR M.S. with 12+ years’ experience OR B.S. with 14+ years industrial experience in biologics purification development with people leader accountabilities.
$237,660 - $307,560ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Abdera Therapeutics Inc. Is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development.
$250,000 - $315,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Your responsibilities will include managing junior RAs/Scientists in addition to working closely with our drug development team (CEO, CSO, Chemists, and Toxicologists) to understand the mechanism of action of our small molecules discovered through our novel platform.
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Masters in science, ideally with a background in biologics, genetic medicines or deep learning methods applied to drug development. Deep understanding of the drug discovery, development and commercialization process, and demonstrated ability to effectively collaborate with R&D and business teams.
$100,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Broad hands-on experience with modern analytical instrumentations commonly used in the analysis and characterization of biologics, carbohydrates, conjugates and small molecule drug candidates and successful track record of method development trouble shooting and validation, e.g., UV-Vis, various modes of HPLC, CE, SDS-PAGE, icIEF, LCMS, GCMS, enzyme kinetics, colorimetric and fluorescent plate-based assays, ELISA, Western Blot, etc.
$150Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Monitors, evaluates and provides advice on process development, compliance and internal controls and provides information and reporting to management. The Operations Manager is responsible for providing assistance in the oversight of business activities, strategic planning and development, and program administration.
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drug development jobs in Belmont, CA
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