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Advise faculty, project directors and financial and administrative staff on proposal submission process, post award administration, regulatory compliance requirements and Institute policy, coordinating with other units supporting research including Conflict of Interest, Research Integrity Assurance, Research Security, Export Control, Corporate Engagement, Technology Licensing, and the Georgia Tech Office of Legal Affairs.
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SummaryThe Regulatory Affairs Specialist will reside within strategic business unit, Huber Specialty Minerals (HSM), at Huber Engineered Materials (HEM). Serve as primary contact for HSM hazard communication support and collaborate with HEM regulatory affairs for SDS/Labeling support.
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Common legal issues handled by USG¿s Office of Legal Affairs include student matters, employment matters (including faculty and staff), contracts, real estate transactions, constitutional issues, legislation, Board governance, litigation support, regulatory compliance, and open government.
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Partner with a variety of Microsoft subject-matter experts (SMEs), including Commerce/Payments & FinTech, Privacy & Regulatory Affairs, Intellectual Property Group, Competition, Office of Critical Infrastructure, Office of Responsible AI, Digital Safety, Environmental Sustainability, and others, to track and interpret regulatory requirements and developments worldwide.
$248,800 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Possible subject matter could include capstone design, regulatory affairs, medical device development, project management, quality engineering, rapid prototyping and design for manufacturability.
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3-5 years of knowledge and experience with a proven track record in Regulatory Affairs and Quality Knowledge in Supplier Quality, Quality, or Manufacturing Engineering, preferably in a medical device environment.
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Join forces with esteemed colleagues across Medical Affairs, Real-World Evidence, Compliance, and Global Medical Information, forming a formidable alliance dedicated to transforming lives. Cultivate deep-rooted relationships with key opinion leaders and regulatory bodies, fostering a symphony of scientific engagement that transcends boundaries.
$232,575 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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4 or More Years of direct regulatory affairs experience, including US labeling experience required. Based on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages, prepares and implements regulatory documents (e.g., USPI, annotated labeling, medication guides, EU SmPC, PIL, CCDS.
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Regulatory / Compliance – strong understanding of the regulatory environment CNB operates in to manage risk and ensure compliance (includes deep knowledge of CIP and KYC) Economic Environment – understanding of the economic environment and its impact on clients.
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LG - Legal, Regulatory & Gov't Affairs. Our Global Legal, Compliance and Regulatory (GLCR) team provides first class advice to colleagues and functions across the organization – ensuring AIG navigates an ever-changing landscape that spans state, federal, and international lines.
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7 or More Years of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs. Experience in providing regulatory strategic input into the Oncology drug development preferred.
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The role will report to a Vice President and Associate General Counsel, Global Risk and Regulatory Affairs, based in Washington DC. Providing legal advice and support to the Value Added Services (VAS) business in connection with Visa's broader Issuing Solutions, Acceptance Solutions and Risk and Identity Solutions teams, across a wide range of complex regulatory and commercial matters and projects, working with colleagues in offices across the world to support the day-to-day legal needs of our internal clients.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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The VP, NSS provides direct leadership of Global Trade Enablement, Government, Legislative, and Regulatory Affairs, NSS AI Excellence functions, and provides local leadership to personnel and resources based in our US offices as required.
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The Regulatory Affairs Specialist will reside within strategic business unit, Huber Specialty Minerals (HSM), at Huber Engineered Materials (HEM). Regulatory Affairs Specialist.
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regulatory affairs jobs in Atlanta, HI, Australia
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