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Excellence in clear, well-documented, and transparent communication on regulatory and/or legislative affairs. Regulatory & Public Power Program Coordinator - Sustainability & Mobility Department - U2380 (UNC.
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The Regulatory and Public Power Program Coordinator (PC) is responsible for tracking and providing analysis on all relevant gas and electric legislative bills, CPUC regulatory filings, or CAISO decisions that may affect the City or residents/business energy bills, City initiatives, and Climate Action Plan goals.
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Build, maintain and advance partnerships with key stakeholders across Regulatory Affairs, Clinical Development, PDM, CMC Regulatory, Quality Assurance, Commercial functions, Information Technology and Development Systems to advance near-term regulatory priorities and long-term innovation efforts with broader enterprise level objectives.
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Join us at Abbvie, in our Maidenhead office as a Regulatory Affairs Manager. As a Regulatory Affairs Manager, you will play a pivotal role in leading a team of Project Managers and Specialists, obtaining, and maintaining marketing approvals for our products in the UK. Implementing the regulatory strategy for the UK. Ensuring full regulatory and company compliance, and provide regulatory expertise to support clinical research, product launches, and business development.
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Executive Vice President and Managing Director, Chief Counsel, Head of Global Regulatory Affairs. Counsel/Senior Counsel, Regulatory Affairs (position title and compensation is commensurate with experience.
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Associate Director, CMC Regulatory Affairs is a hands-on and independent role requiring a strong individual who will provide strategic and operational support to multiple programs, with an emphasis on CMC (Chemistry, Manufacturing, and Controls.
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Regulatory Affairs Manager (Medical Device/Cosmetic) - Long Beach, California page is loaded. Regulatory Affairs Manager (Medical Device/Cosmetic) - Long Beach, California. Serves as the internal subject matter expert for international regulatory affairs on assigned projects/regions, including labeling review.
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Were a leader in staffing Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, HEOR, Market Access, and Sales & Marketing roles. A growing molecular imaging company is seeking a Medical Science Liaison (MSL) to join its Neurodegenerative Diagnostics team covering the Great Lakes territory.
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Collaborates with Government Regulatory Affairs, Network Management, Medical Economics, Benefit Administration, Provider Services, Audit, IT and Claim Operations to determine the impact of implementing policy changes.
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The TeamAmongst its other responsibilities, the Global Strategy, Regulatory and Public Affairs team leads on the development and implementation of Gates Ag One's regulatory science programs and related activities, such as regulatory studies, permit acquisition, and ensuring compliance with phytosanitary and biosafety regulatory requirements.
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Cleveland State University seeks a dynamic, forward-thinking academic leader to serve as the next dean of the Levin College of Public Affairs and Education. Job title: Dean, Levin College of Public Affairs and Education (Cleveland State University.
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Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for developing strategies to obtain FDA clearance or approval of new Class II & III cardiovascular medical devices and improvements to existing devices.
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Senior Regulatory Affairs Specialist. Be passionate about Regulatory Affairs impact in support of the research, development, clinical, marketing, and production of state-of-the-art class III cardiovascular medical devices.
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Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society) Regulatory affairs experience in the medical device industry with a track record of successful submissions.
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Experience in reviews of engineering, manufacturing, marketing, labeling and clinical documents for regulatory compliance. You will advise on regulatory requirements as a key member of cross-functional teams, prepare and review FDA submissions, and interact with and respond to FDA pre-submission and during the review period.
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regulatory affairs jobs Title: intern Company: Apco Worldwide
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