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The Federal Regulatory Affairs Manager will collaborate closely with the North America Team Leader and business-lead Vice Presidents to develop regulatory strategies to ensure registrations are obtained and maintained to meet business objectives and timelines.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Serve as a liaison between the hospital and regulatory agencies during inspections and audits, provide functional direction to collaborate with risk and regulatory affairs to ensure reports are provided for regulatory reviews and the program meets regulatory needs as outlined in standards.
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Master’s degree in a related field such as engineering, regulatory affairs, or physics, or equivalent combination of education and experience. Regulatory communications liaison between NRC and MURR, including crisis communications (24-hour timeline) during event.
$161,595.2 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Director of Regulatory Affairs is responsible for planning, organizing, implementing and evaluating regulatory compliance initiatives to support patient safety and quality and ensure continuous compliance with Federal, State and local regulatory requirements.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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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.
Full-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Certifications: American Society for Quality (ASQ) or Regulatory Affairs Professionals (RAPS) certificates or similar are preferred. Certifications: American Society for Quality (ASQ) or Regulatory Affairs Professionals (RAPS) certificates or similar are preferred.
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Collaborate Cross-Functionally: Work collaboratively with internal and external stakeholders, including regulatory affairs, clinical research, quality assurance, and IT teams, to achieve project objectives and deliver high-quality solutions that meet business needs and regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Responsible for obtaining, assembling, and forwarding all required documents and records for the active duty, AFRC, and ANG to the Veteran Affairs Medical Service Coordinator, the local MEB, the IPEB, the FPEB, and other IDES stakeholders in accordance with regulatory guidance.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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This position performs regulatory compliance reviews and examinations of financial records of mortgage loan brokers, continuing care retirement communities, credit counseling/credit repair businesses, physical fitness centers, pre-need funeral contract facilities, pawnbrokers, and other specialized investigations or examinations.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The role requires strong skills in colleague / team leadership / development as well as collaboration and project management with internal ISS leaders, institutions and other department including, Finance, Regulatory Affairs, Internal Audit, and Marketing.
$175,761.84 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Collaborate with regulatory affairs teams to understand and address regulatory requirements for pharmaceutical product evaluation, submission, and approval processes. Stay Current on Industry Trends: Stay abreast of industry trends, regulatory changes, and best practices related to drug evaluation and regulatory affairs.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience in regulatory compliance, performance/quality improvement, patient safety, risk management or project management preferred. Coordinating virtual and onsite surveys by external regulatory/accreditation agencies.
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The Executive Director oversees all aspects of the agency’s operations, including licensure, survey, and certification activities; administration; fiscal services; human resources; information technology; quality improvement; government and regulatory affairs; emergency preparedness; quality initiatives; and strategic planning.
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Environmental experience in policies and procedures, regulatory affairs, permitting, due diligence, and auditing. 10+ years of environmental regulatory experience managing and implementing environmental programs.
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Additional non-pharma sponsored duties may include product investigation support, internal and external audits (partner, regulatory) and to support, as needed, Regulatory Affairs functions in support of CDx projects and filings.
$158,268 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
regulatory affairs jobs in Columbia, KS, Germany
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