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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.
$206,469 - $309,703Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Director, Business Development, is responsible for identifying and enabling growth opportunities for the company. Lead strategic research and business development initiatives to identify and establish high-impact opportunities and partnerships.
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The natural and physical sciences, engineering, and medicine, who are exploring nanoscale properties and devices with potential applications as diverse as water purification, energy conservation, drug delivery, and national security.
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Demonstrated in-depth knowledge of drug development, from preclinical to late-stage development, including experience submitting BLAs and MAAs to the FDA and EMA. 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.
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To support therapeutic programs within BigHat’s drug discovery pipeline. Design, develop, and execute in vitro/ex vivo cellular assays utilizing a variety of experimental methods (e.g., flow cytometry, live cell imaging, ELISA, etc.
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
$180,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Maplewood Senior Living conducts pre-employment screening including background check, drug screening, and reference checks. Participation in assessments under the supervision of the Resident Services Director (RN.
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We are seeking an innovative and motivated Senior Scientist I to develop and implement novel capabilities and assays (in particular those related to bacterial targets) to functionally characterize our therapeutic antibody drug candidates, and to help spearhead projects to continually improve and expand upon our internal capabilities.
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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. Well versed in FDA, EMA and ICH guidelines relating to registration, quality, and compliance concerning drug substance and authored CMC sections in commercial filings (BLA, MAA) and post approval changes.
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Our 2022 Annual Security Report also outlines various campus safety and security policies, such as those concerning crime reporting, prevention and response to sexual and gender violence, alcohol and drug use, crime prevention, emergency response and evacuation procedures, and other matters.
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Demonstrated experience in establishing supply chain strategies and workflows for autologous or allogeneic cell therapies including, but not limited to, materials management, labeling for GMP (Good Manufacturing Practices) drug product, cold chain management, and demand and supply planning.
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Major clinical programs at McLean address a broad range of illnesses including depression, bipolar and psychotic disorders; mood and anxiety disorders; alcohol and drug abuse; Alzheimer's disease, and child and adolescent psychiatric disorders.
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Each plan includes 100% coverage for preventive care, telemedicine through Teledoc, prescription drug coverage, and behavioral health coverage. Responsibilities include interviewing, hiring/firing, scheduling, performance evaluations, quality reviews, timecard reconciliations, staff education, coaching, development, support and promotion of customer relations, and monitoring of activities to ensure performance standards are achieved.
$66.46 - $88.05 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Director, Project Management, the Associate Director, Project Management is responsible for managing cross-functional drug development projects, in either preclinical or clinical development stages.
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The candidate's main focus is development of device fabrication process for next generation DNA sequencing consumable cells. Pacific Biosciences is looking for an experienced individual to join the SMRT Cell Process Development team working on R&D for next generation devices.
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drug job Title: development director Company: Omeros in Redwood City, CA
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