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Our Gene Therapy facility, located at the University of Maryland (UMD) BioPark in Baltimore, MD, specializes in upstream and downstream process development of viral vectors for clinical applications.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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Position Overview: As a Senior Scientist in the Upstream Process Development Department, you will be responsible for leading the design, optimization, and scale-up of upstream processes. Extensive experience with small-scale and large-scale cell culture bioreactor process development.
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We are seeking a highly motivated, independent scientist to join our Development, Optimization & Implementation team to establish and support new pipelines for extraction and downstream technologies required to support DCEG investigators in areas of human, bacterial, and viral nucleic acid research applications including metagenomics, targeted sequencing applications, and ctDNA and cfRNA sequencing.
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Design & develop Java/JEE components w/ JAX-RS, Spring Boot. Provide unit and development level integration testing. Over 5 years of Java/JEE development with Spring REST, JAX-RS and Spring Boot.
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We are currently seeking a highly motivated and experienced Senior Scientist to join our Downstream Process Development group. Senior Scientist - Downstream Process Development.
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We are seeking an Associate Scientist to join our Downstream Process Development group in Gaithersburg, MD. Qualified individuals will be responsible for hands-on execution of downstream chromatography and filtration processes in support of process development, scale-up, process characterization activities, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines.
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Provides insight and supports the development and implementation of business initiatives, systems, and/or processes to a desired future state by maintaining a working understanding of how current processes impact business operations; mapping current state against future state processes; identifying the operational impact of requirements on upstream and downstream solution components; and identifying and validating value gaps and opportunities for process enhancements or efficiencies.
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Working knowledge of cryptography, secure communications, secure software development practices. The role shall continually develop technology-forward, cutting edge software solutions to address the backend and the downstream systems including website and mobile app goals as well as to create and manage APIs that work across devices, and multiple external partners.
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Perform technical requirements decomposition of initiatives that inform downstream feature development and deployment by service teams. Description Leidos is seeking a Systems Engineer to support a development program responsible for delivering modern Identity Access Credential Management (ICAM) solutions and Zero Trust Architectures (ZTA.
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The Systems Engineering Lead will lead the engineering teams, for a large government contract task order, in taking a multi-discipline approach to requirements engineering, solutions engineering, scheduling, reliability, resiliency, services development, integration, test and evaluation, maintainability and analysis across the Task Order.
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Electronically platform provides SOA based web services of web applications for secured public-facing access to downstream processing of secured information. 2 years working with Redhat OpenShift.
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A proven track record of 2-4 years of relevant experience selling a portfolio of contract manufacturing services including upstream and downstream process development, cell/virus banking, GMP biologics manufacturing, GMP aseptic filling, QC release and stability testing, etc., to biopharmaceutical clients is required.
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The successful candidate will play a crucial role in leading drug substance purification process development, scale-up, and technology transfer activities for the pipeline molecules, contributing to the successful manufacturing of biopharmaceutical products, with a specific expertise and focus on antibody-based molecules including antibody-drug conjugates (ADCs), bispecific antibodies and fusion proteins.
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Assist with technology transfer from Process Development to manufacturing environment. The Manufacturing Associate II/III participates in the cell culture manufacturing of biopharmaceutical drug substance to support multiple clinical programs.
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downstream development jobs in Potomac, MD
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