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Support the Public affairs team’s writing and material production to educate internal and external stakeholders on the impacts of current and proposed regulatory and legislative changes. Under the direction of VP, Public Affairs, the Strategic Relationship Lead, External affairs acts as a key member of the Government Relations and Public Affairs team’s efforts to build strength to impact public policy on behalf of Novant Health.
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QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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The Sr. Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects and review issues related to regulatory documents, investigations, product development planning and regulatory agency interaction.
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Experience working with legal counsel on regulatory and legislative affairs. The Virtual Power Plant Policy Director will lead SUN’s policy, regulatory, and advocacy efforts to implement solar + batteries Virtual Power Plant (VPP) policy across the country and in targeted states.
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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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The Regulatory Compliance Analyst/Specialist (RCS) will be responsible for tracking regulatory developments globally in the US at both federal and state level as well as certain other designated countries if required and inputting this information into our online database ‘C2P’ (Compliance to Product) in a structured format, providing an overview of the regulatory information and identifying key details such as when the measure enters into force & upcoming compliance deadlines.
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Shape, lead & advance US regulatory policy & advocacy efforts of interest to UPL in enabling US grower access to innovative technologies. JOB SUMMARY: UPL is seeking an experienced Government Affairs & Industry Relations leader to be responsible for engagement with US Federal and State government, grower organizations and industry/trade associations to influence outcomes affecting the UPL NA business as well as support policy and legislative activities through industry partnerships.
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The Associate Director, Regulatory Affairs (CMC) possesses strong leadership skills, broad knowledge of multiple aspects of regulatory affairs (beyond CMC) across all phases of drug development, and a deep understanding of global CMC regulations, including GMP and region-specific guidelines, especially as they relate to gene therapies.
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Knowledge of major regulatory areas of focuses including Consumer Compliance Regulations, FFIEC Guidance, Stress Testing, Model Risk Management, Capital Planning and Forecasting, Enterprise Risk Management, and Operational Risk Management, Data Governance, etc.
$240,000 - $320,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This role will interact with cross-functional teams, including colleagues from Clinical Operations, Biostatistics, Clinical Data Management, Medical Affairs, Regulatory Affairs, Research and others.
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1035 Public Affairs Specialist. Disabled veterans rated by the Department of Veterans Affairs (VA) as having a compensable service-connected disability of 30 percent or more. 1084 Visual Information Specialist.
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Strong knowledge of US EHS related regulatory requirements (e.g., EPA, OSHA, NIOSH, ANSI, and NFPA rules, regulations, and standards) and their application to a laboratory environment (e.g., environment, waste management, sustainability, hazardous material/dangerous goods transportation, EHS management systems.
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System Office staff is responsible for executing the policies of the UNC Board of Governors and providing University-wide leadership in the areas of academic affairs, business and financial management, long-range planning, student affairs, research, legal affairs, and government relations.
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Support regulatory exercises such as CECL, IFRS9, CCAR/DFAST. carry out and document independent model validation in line with regulatory requirements and internal standards. familiarity with Basel Regulations, CECL, IFRS9, CCAR is a plus.
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Work in the Global Rare Diseases, Regulatory Affairs Ad Promo function for the United States, with additional duties in Canada. Minimum 5 years Pharmaceutical/Biotechnology industry experience, at least 3 years Regulatory Affairs and advertising and promotion review and approval experience with marketed prescription drugs.
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regulatory affairs jobs Company: Jobget in Cary, NC
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