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As a Program Manager, you will be accountable for directing customer support services, engineering, program management/ Project Management Office (PMO) and strategic support activities across all aspects of the program, including Service Desk, Deskside/ White Glove Services, systems engineering, Low Code/ No Code, DevSecOps, Automation, Hybrid cloud infrastructure, and cybersecurity, engineering.
$122,200 - $220,900 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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CSS is seeking a highly qualified candidate(s) for a GIS Analyst / Product Development Specialist on an interdisciplinary research team of contract and federal employees. We seek a qualified candidate(s) to support GIS data analysis, data archival, and data visualization product development for public consumption.
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The process development scientist will support product development strategies to create new and innovative synthetic biology-based cellular medicines. Rise Therapeutics is recruiting an experienced full-time process development scientist with a background in bacterial fermentation to work in our Rockville, Maryland laboratory.
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The qualified individual should have demonstrated proficiency with development and application of HPLC, LC/MS and/or Size Separation based methods for phase-appropriate characterization of protein or vaccine products, including but not limited to peptide mapping, size-exclusion chromatography (SEC), residual assays, and intact mass determination via high-resolution LC/MS analysis.
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The Manager of Donor Relations & Operations provides executive level support to the President & CEO and the Westminster Ingleside Foundation (WIF) Board of Directors. The manager will lead the back-office operations, database management, and coordinate with the WIF team, and Ingleside Finance office.
$80,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Description: The Supplier Quality Manager-Sr Manager is responsible for management of systems and processes supporting Altimmune's oversight of its GMP suppliers. Serve as a QA lead on combination product development projects and oversee risk management activities.
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International Development Division (IDD) We advance evidence in the areas of education, health, the workforce, human services, and international development to create a better, more equitable world.
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GSK is currently looking for an Operational Quality Manager to join our team in Rockville, MD. OQ Manager will be responsible for Operational Quality’s day to day activities at LSM/SSM site including batch record review and day to day Quality Operations.
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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. Job Advertisement: Senior Scientist Upstream Process Development.
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Computercraft is looking for a dynamic Product Manager to join a team that helps develop and manage cutting-edge digital products at the National Center for Biotechnology Information (NCBI), part of the National Library of Medicine (NLM) at the National Institutes of Health (NIH.
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Bioassay development of GMP release assays, product characterization assays, support stability and in-process testing of a wide range of bio therapeutic modalities, including: Viral vectors, monoclonal antibodies (mAbs), ADCs, bi-specifics, cell & gene therapy, and other biologics.
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Leads proposal development efforts, serving as Proposal Manager for specific opportunities, including proposal kickoffs, color team reviews, and final proposal compliance and quality assurance.
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The QC Microbiology Manager is committed to supporting GSK global biologics analytical network with reliability, integrity, active engagement, and cross functional collaboration. Under the direction of the QC Microbiology Associate Director, the QC Microbiology Manager is responsible for supervising and providing guidance to the team of the QC Microbiology laboratory to complete laboratory testing and testing support activities, while creating an inclusive culture that energizes a Safety First, Quality Always, with a continues improvement mindset.
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This individual will play a leading role on upstream process development including supervise a team of scientists/research associates; maintain insect cell culture, BVI and recombinant protein production, and write technical reports, etc.
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Several years of relevant experience in immuno-oncology, oncology and/or infectious diseases in a biotech/pharmaceutical and/or academic environment, including leadership of clinical development activities, ideally from exploratory Phase I/II clinical trials through late stage development in Phase III and NDA submission.
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Title: development manager Company: Isee in Rockville, MD
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