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This includes cycle count program development, master data management, material replenishment, and third-party logistics management. As a member of Site Supply Chain, the Inventory Specialist will directly support Materials Management, Site Planning, Procurement, Supply Chain systems, and compliance.
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Learning Specialist at Jewish Community Day School. As our K-8 Learning Specialist you will support students with executive functioning difficulties, a variety of learning disabilities, ADHD, and social emotional difficulties.
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This is a senior-level position that requires a deep understanding of the financial markets, exceptional networking skills, and a strong background in commercial real estate development. Coordinate and manage regional & international travel arrangements for investor presentations with WS Development senior leadership.
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Desired Qualifications: B.S or M.S. Degree in Civil Engineering Licensed Professional Engineer (PE), or (EIT) 3+ years of demonstrated engineering design of Land Development Projects Utility Design Site Grading Storm Water Management Systems Zoning Research Permitting Research Proficiency with AutoCAD, Civil 3D software Salary and Benefits: Comprehensive Salary Package.
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POSITION REPORTS TO Director of Content DURATION This is a one year temporary full time hire eligible for our amazing benefits package (100% company paid health care, PTO, 403b, lifestyle and professional development stipend) SALARY $62-72K APPROXIMATE START DATE ASAP LOCATION & POLICY ON REMOTE WORK This role is completely flexible to be fully remote, hybrid, or onsite, whatever works best for you.
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Our areas of expertise include behavioral health, mental health policy and services, substance use disorders, workforce development, homelessness, housing and employment programs, trauma-informed care, criminal justice, women and children, veterans, health care reform, and population health management.
$56,000 - $61,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Alloy Global Bioanalytics group provides bioanalytical support to all Alloy activities, including assay development, quality control and high-throughput characterization of antibodies, TCRs, TCR mimics and.
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Key research areas include the development of electrochemical and other techniques to characterize ageing and damage mechanisms of Li-ion batteries, such as Li plating/stripping, dendrite growth, and internal resistance changes prior to thermal runaway and electrical failure.
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You may directly manage and/or serve as a matrix manger of senior Bioanalytical Development leads, ensure development of sound bioanalytical assay designs and implementation by working closely with iBA scientific and technical staff in the lab as well as with cross-functional stake holders.
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Strong knowledge of pharmacokinetics and pharmacodynamics principles, immunogenicity, modeling and simulation, Model-Informed Drug Development, ADME Concepts, and regulatory clinical pharmacology requirements to support clinical development and regulatory submission.
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Experience in functional management of reliability engineering, code compliance, standards compliance, engineering team members who are engaged in product development on projects from initial concept, through development and verification / validation testing, and into Manufacturing.
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BS with 2-5 years or MS with 0-2 years of relevant industry experience in analytical development. Work collaboratively with other colleagues in Analytical and Technical Development as well as other cross-functional teams to support stability related business needs.
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The Video and Multimedia Production Specialist is part of a team of communications professionals who develop and deliver impactful communications to engage Thermo Fisher Scientific partners around the world.
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This role is suited for an R&D engineer with experience in developing, building, and testing complex electro-mechanical medical devices, design transfer, and process validation with broad knowledge of electrical, mechatronics, firmware, software, and systems engineering, including design verification testing, and transfer to manufacturing within a regulated medical device development environment.
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Strong knowledge of pharmacokinetics and pharmacodynamics principles, immunogenicity, modelling and simulation, Model-Informed Drug Development, ADME Concepts, and regulatory clinical pharmacology requirements to support clinical development and regulatory submission.
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