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Bachelor of Science, International Affairs/Foreign Affairs or similar field with 4+ years of relevant experience OR a Master of Science, International Affairs or similar field with 2+ years of relevant experience.
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Make a difference in national security as a program analyst within the National Nuclear Security Administration (NNSA) Defense Programs’ Office of International Programs in Washington, DC. This office supports international collaboration under Mutual Defense Agreements (MDAs) and advises on export control issues.
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Partner with a variety of Microsoft subject-matter experts (SMEs), including Competition, Privacy & Regulatory Affairs, Intellectual Property Group, Customer Security and Trust, Office of Responsible AI, Digital Safety, Environmental Sustainability, Commerce/Payments & FinTech, and others, to track, interpret, and identify trends in regulatory requirements and developments worldwide.
$268,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The C+AI Trusted Platform Legal Team provides legal support to the compliance engineering team that drives legal and regulatory compliance programs, initiatives, and requirements across the enterprise products and services in the C+AI business division at Microsoft, including Azure, Dynamics 365, and Power Platform.
$268,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Communicate regularly and effectively in a cross-functional matrix with development, origination, fundamentals, finance, and political & regulatory affairs staff to translate regulatory and market issues into business impacts and opportunities to benefit the position of Pattern's new and core business interests in MISO and other priority markets.
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Agency: ACADEMIC AFFAIRS. Old Dominion University (ODU) invites applications for a Clinical Assistant Professor faculty position in the Medical Laboratory Science Program of the School of Medical Diagnostic & Translational Sciences beginning July 25, 2024.
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Principal Duties & Responsibilities Develops and supervises global Regulatory Affairs support function to leverage Subject Matter Expertise (SME) for completion of Customer requests, Regulatory Responses, Product Dossier maintenance, and Document Control related to pharmaceutical, food, personal care, automotive, polymers, and industrial applications.
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Regulatory Compliance: Stay informed on evolving tax regulations and policies impacting renewable energy incentives, such as the Investment Tax Credit (ITC) and Production Tax Credit (PTC). Technical Proficiency: Knowledge of renewable energy tax incentives and regulatory frameworks, including ITC and PTC.
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The CMC Regulatory Affairs Sr. Manager at Gilead is responsible for providing strategic direction, operational support, and technical expertise for. Initiates process improvements and contributes to global process improvements, which have a significant impact for the Regulatory Affairs CMC Department or development matrix teams.
$199,320 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Advanced life science degree or certification in Regulatory Affairs Sciences preferred. Experience and solid knowledge of Pharmacovigilance specificallyProficiency in one or more of these additional areas is a plus: CMC/Mfg., Clinical development and trial execution, Regulatory, Real-World Data and Real-World Evidence, Cell and Gene Therapy, Medical Device, IVD/CDxExperienced in understanding and interpreting regulatory guidelines and documents.
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Ensures quality management of the clinical appeal process to reduce the risk of State and Federal Regulatory fines and sanctions, avoid adverse exposure, reiterate the expectation of a fair and compliant appeal process for our membership, and support NCQA accreditation and the Divisional Goals for Care Management.
$174,042 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Technical Expertise: In-depth knowledge of KYC/AML processes, regulatory requirements, and related technologies. If you are passionate about leveraging technology to drive regulatory compliance and innovation, we invite you to apply for the CTO position.
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Collaborate with cross-functional teams, including analytical development, formulation development, quality assurance, and regulatory affairs, to ensure seamless project progression. Collaborate with regulatory affairs to support regulatory submissions and inspections.
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New product setup and management of related projectsAssist with Supplier audits, as neededMaintenance of BSE Serum Certificates of Suitability filing with EDQMCollaborates with USDA on regulatory compliance activities including regulatory approvals, import/export compliance, traceability, quarantine, safety testing and affidavits.
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As the Director of Regulatory Compliance (MLRO), you will be working as part of Nium's global, dynamic Compliance team and will be reporting to the VP Compliance (US). Perform ongoing AML and OFAC risk assessments and horizon scanning for applicable regulatory requirements.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago
regulatory affairs jobs Title: principal Company: Parexel
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