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Coordinate with Financial Aid, Student Affairs, and Academic Affairs to accurately calculate individual student withdrawals. The college offers bachelor's degrees in fourteen disciplines including arts entrepreneurship, design, fine arts, and media arts; one MFA; three online master's degrees; and continuing education classes for all ages.
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The Marketing and Engagement Team (MET) is led by Alight's Chief Marketing & Engagement Officer (CMEO) and is comprised of several teams: Annual Fund, Global Connections/Major Gifts, Donor Services, Marketing & Communications, MET Operations, and Global Partnerships & Government Affairs (PGA.
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Members of the Institutional Advancement team engage with nearly every department within the law school such as the Dean and Associate Deans, senior administrators, faculty members, the Office of Communications, the Office of Career Services, the Office of Student Affairs, and more.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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Cross-functional Collaboration with various departments, including logistics, finance, Tax, legal, finance, Govt Affairs, ITQ/FSQ, Global Security, External Supply Chain, and Sourcing, to align global trade practices with overall business objectives.
$135,300 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Opportunity Abbott is seeking a passionate, experienced Senior Regulatory Affairs Specialist to join our team on-site in Plymouth, or St. Paul, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems.
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Regulatory affairs certification (RAC) or relevant professional certification (e.g., ASQ Certified Quality Auditor) preferred but not required. Collaborate with cross-functional teams, including manufacturing, quality assurance, quality control, regulatory affairs, and supply chain, to address GMP-related issues and drive continuous improvement initiatives.
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This role will work closely with cross-functional partners including marketing, medical and scientific affairs, sales teams, regulatory, R&D, finance, and global partners. Partner with Brand Activation and the Tradeshow Channel Manager to communicate brand messaging and content at key IR meetings, Innovation Center visits and when targeting competitive accounts.
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Minimum of 5 years of pharmaceutical industry experience in a Quality Assurance and/or Regulatory Affairs function including experience in manufacturing and control of solid dosage form drug products and bulk drug substances.
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Principal Regulatory Affairs Specialist. Job Segment: Regulatory Affairs, Compliance, Pharmaceutical, Product Development, Technical Writer, Legal, Science, Research, Technology. Acts as a primary Regulatory Affairs representative in Material Controls, Supplier Quality and Medical Electrical Equipment spaces.
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This position works closely with the MAC Building Official and the Environmental Affairs Department for project execution and compliance. This position coordinates work efforts closely with the Airport Development Director of Project Initiation and Grants Manager.
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The ideal candidate will have 2 or more years' experience as a banking regulator and/or at a large financial institution, Big 4 Public Accounting or advisory or law firm leading regulatory affairs and/or exam management activities.
$129,900 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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As a Sitecore Engineer, you will play a critical role in implementing and maintaining robust, full-stack solutions that support our internal Public Affairs department. Strong understanding of CI/CD concepts and tools (e.g. Azure DevOps.
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Digital Transformation of Submissions: Collaborate with the Regulatory Affairs team to convert paper-based IND submissions into a standardized electronic format, ensuring compliance with FDA and other regulatory body requirements.
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This role involves close collaboration with cross-functional teams, including R&D, regulatory affairs, and quality assurance, to ensure the successful execution of clinical studies. Clinical Research Associate/ CTMPosition Summary: The Clinical Research Associate (CRA)/ CTM will oversee and manage clinical trials to ensure compliance with regulatory requirements and study protocols.
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affairs job in Brooklyn Center, MN
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