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CECL, Part 30 core capabilities initiatives, stress test and CCAR regulatory requirements, etc.) This may include regulations related to specific product or macro / systemic regulation, including standards to comply with Basel II / III, MiFID, U.S. Fed, Treasury, FDIC and regulations from other central banks and regulatory authorities.
$113,840 - $170,760 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Minimum of 10 years’ experience in Regulatory Affairs or Strategy or similar field required, including experience with Marketing Applications (FDA and/or EMA) and FDA REMS. College graduate in Biological Science, Public Health, or Regulatory Science or related field, or related experience, Masters or PhD preferred.
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Research, analyze, and respond to inquiries, litigation (mediation and arbitration), regulatory actions, complaints, appeals, etc. Your primary focus will be to professionally evaluate and respond to issues, protect the companys image, safeguard assets, and mitigate regulatory actions and examinations.
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In addition, the GFC Governance function plays a critical role in liaising with AML and Sanctions officers of FIS’s subsidiaries as well as other Risk and Compliance functions across the Legal, Compliance & Corporate Affairs division at FIS.
$84,720 - $142,320 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are looking for a dynamic person to join our in-house team as a Senior Regulatory Affairs Program Lead - Medical Devices to join their internal team in the United States. You will be responsible to administer day-to-day Regulatory Affairs department activities by directly or indirectly managing individual employees, teams of employees, or third-party vendors.
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Ensures alignment with the multi-segment business model; Partners with the Enterprise Strategy team to implement the appropriate business model, facilitating information exchange and issue resolutions between the Execution Team and Work Streams, shared services partners and regulatory and legislative affairs teams.
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This position helps ensure all maintenance activities are carried out in accordance with regulatory standards, manufacturer specifications, and JTA policies and procedures. A track record in budget management, stewardship and developing proven strategies to build multi-faceted external affairs and development programs.
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Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. The Quality Control Analyst is responsible for reviewing Medical Disability Examination (“MDE”) reports and Disability Benefits Questionnaires (“DBQs”) generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the “VA.
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The primary responsibility of this individual is to administer day-to-day Regulatory Affairs department activities by directly or indirectly managing individual employees, teams of employees, or third-party vendors.
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We provide a complete turnkey service managing environmental affairs involving emergency spill response, remediation, regulatory reporting and waste management. We provide a complete turnkey service managing environmental affairs involving emergency spill response, remediation, regulatory reporting, and waste management.
$18 - $21 an hourFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Researches and provides consultation on requests from internal business partners such as Corporate Legal and Regulatory Affairs, Sales, and Segment. Communicates and collaborates effectively with cross-enterprise business areas (e.g., Corporate Legal and Regulatory Affairs, Sales, Segment, and ASO partner platforms) as appropriate throughout the contract development and review processes to ensure all compliance, regulatory and project deadlines are met.
$74,200 - $120,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams including regulatory affairs, quality assurance, and clinical operations to ensure alignment of clinical development plans with overall project goals.
$70,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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4+ years of experience in medical device regulatory affairs with roles showing increasing responsibility. Act as Regulatory Affairs representative on project transfer teams.
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He/she also partners with leaders in multiple departments including R&D, Clinical Sciences, Medical Affairs, Regulatory Affairs, and Global Strategic Marketing in support of the execution of clinical research strategies.
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The incumbent will perform program analyses to evaluate efficiency and effectiveness of program practices impacting Native American Tribes, legislative and regulatory issues relevant to HHS and IHS.
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regulatory affairs jobs in Jacksonville, Sherwood, Canada
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