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7+ years of experience working with the state Legislature, the Executive Branch, municipal government officials, government relations, public policy, advocacy, government affairs, or campaigns. The Vice President, State Government Affairs will be part of the UHG External Affairs organization, responsible for working with colleagues across External Affairs and the Company to develop and implement strategies on the company's declared state government advocacy, growth, relationship and reputational priorities and overall business advancement initiatives with key state policymakers.
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High School Diploma/GED from AND ten (10) years of (combined product stewardship, regulatory affairs, or EHS experience in a private, public, government or military environment. Bachelor’s Degree or higher AND three (3) years of combined product stewardship, regulatory affairs, or EHS experience in a private, public, government or military environment.
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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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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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10+ years of experience in quality assurance and regulatory affairs, with a significant portion in medical device, or advanced manufacturing industries. As the VP, Quality & Regulatory Affairs, you will lead all aspects of quality assurance and regulatory compliance across the Global Enterprise.
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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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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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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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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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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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Position Summary: As a member of the Regulatory Operations team, the Regulatory Affairs Specialist II completes regulatory submissions related to market expansions as well as sustaining product line international regulatory renewal activities.
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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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The individual for this role should have capability and confidence to lead cross-functional teams which may include but is not limited to: mechanical/electrical design, software, quality/reliability, verification/validation, human factors, systems engineering, process development, supplier quality, sourcing, and regulatory affairs.
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The individual for this role should have capability and confidence to lead cross-functional teams which may include but is not limited to: mechanical/electrical design, software, quality/reliability, verification/validation, human factors, systems engineering, process development, supplier quality, sourcing, and regulatory affairs The ideal candidate has 3+ years leading programs of a similar nature within a highly regulated field, medical device preferred.
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affairs job Company: Biophase in Golden Valley, MN
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