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The Counsel position will be an integral part of the Regulatory, Operations, Government Affairs and Environmental team. The Counsel will assist the Deputy Chief Counsel and Principal Counsel on various transactional, operational and regulatory legal matters primarily for Disney Signature Experiences (with a focus on Disney Cruise Line) and also the Walt Disney World Resort.
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The VP leads a team of professionals across multiple cities to influence the regulatory affairs/advocacy agenda for hydrocarbons and biofuels, owns key strategic relationships internally with the Communications & External Affairs team and externally with various trade associations, and promotes the physical regulatory reporting responsibilities for all commodities (a key license-to-operate function.
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5 + years of experience in global CMC regulatory affairs. Key responsibilities include leading the preparation and maintenance of CMC/quality sections for regulatory submissions, serving as the CMC regulatory representative on project teams, and providing regulatory assessment and guidance on CMC-related change controls, deviations, and investigations throughout the product lifecycle.
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The Federal Regulatory Affairs Manager directs US Federal regulatory package/dossier development, product registration, and lifecycle management of all Certis Biologicals products.
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Lead individual giving prospect research, tracking new opportunities and solicitations in Salesforce and working with the Managing Director of Development to qualify new prospects that come through board members, meetings, and individual research.
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The Analyst II, Regulatory Affairs has experience with and performs key centralized complex and difficult regulatory activities for the Compliance Department. Knowledge of and experience with state and Federal regulatory and other requirements and practices related to Covered California, Medicare and Medi-Cal (Medicaid), Title 19 (USC)/Title 29 (USC and CCR), Title 22 (CCR), Title 28 (CCR), Title 42 (USC and CFR), CA Welfare and Institutions Code, and CA Health and Safety Code.
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Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance.
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Years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment. Maintain up-to-date knowledge of current and future product stewardship, chemical regulatory compliance, and sustainability issues through membership in trade associations and external committees, regular review of relevant publications and subscription services, and interactions with external experts and advisors.
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Contribute to the development and implementation of resource mobilization strategies for UNICEF’s humanitarian action for children, focusing on quality and flexible funding. The Humanitarian Partnerships and Financing Officer would be part of the Humanitarian Partnerships and Financing Team in PPD. Under the supervision of the Team Lead, the Officer will contribute to the humanitarian financing policies, mobilization, management and development of resources and partnerships for UNICEF’s humanitarian action.
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As a CMC RA Associate Director Project Leadership, you will provide regulatory CMC knowledge and progressively increasing levels of expertise to TA and non-TA projects within Global Regulatory Affairs(GRA) and AZ technical functions.
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Reporting to Zufall Health’s SVP of External Affairs, the Development Director functions as a member of a dynamic development team within a robust and innovative community health system who is integral in the identification, cultivation, and management of individual and corporate donors to the Zufall Health Foundation and Zufall Health Center.
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Summary You will serve as the SUPERVISORY PROGRAM DEVELOPMENT AND LEGISLATIVE AFFAIRS MANAGER in the Planning, Design, and Construction of the Naval Facilities Engineering Command of NAVAL FACILITIES ENGINEERING SYSTEMS COMMAND. Duties.
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The Staff Attorney (Legal Affairs) is responsible for providing legal research, analysis, drafting support and other legal services to staff covering a wide array of legal matters that may arise in the multifamily industry.
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Reporting to the Senior Director for Federal Affairs, the Senior Manager will assist with research and direct lobbying to support AIA’s federal legislative agenda. In collaboration with the Senior Director for Federal Affairs, coordinate with key staff members to build grassroots and grasstop support for AIA’s advocacy agenda.
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The employee will support the Deputy Director for Office of Policy Planning and Coordination, Strategy and Resources Unit in the Bureau of Western Hemisphere Affairs with expert program planning, execution, and monitoring; communicate program objectives and policies; oversee training needs; monitor foreign assistance performance; coordinate policy issues; and track and coordinate foreign assistance grants.
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regulatory affairs research and development jobs Title: medical director Company: Glaxosmithkline
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