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With minimal oversight, the Pr. Regulatory Affairs Specialist (PRA) for the European Union Medical Device Regulation (MDR) will be responsible for supporting execution to MDR compliance plans to ensure all applicable technical files (for devices ranging from class I to class III) meet the EU MDR requirements on schedule.
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Support the Fintech business in the adoption of enterprise risk and compliance framework of policies, testing, training, and reporting. Monitor and maintain awareness of regulatory changes relative to the Fintech products and services and work; support the Chief Compliance Officer in efforts to achieve compliance with regulatory changes within Fintech.
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The person will work directly with stakeholders across – ESG Investments, ESG Product Strategy, ESG Data and Operations, Client, Product and Regulatory Reporting, and Enterprise Risk Management to understand their data and reporting requirements and to translate requirements into functional specifications for technology partners building/ enhancing IT solutions for ESG reporting.
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Experience selling one or more of the following: Analytics, Back Office Solutions, Data Governance, Data Management, Data Warehouse, EOD Reporting, Front Office Solutions, Managed Services, Middle Office Solutions, Order Management (OMS), Portfolio Management (PMS), Reconciliation, Regulatory Solution, Reporting, Trade Management, Treasury.
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Develop and maintain HSSE related KPI’s and ensure compliance and reporting as required with all regulatory agencies (FERC, PHMSA, CFR, etc. Lead role in the development, implementation and operationalizing of RGLNG Safety Case, Regulatory Compliance Plan, Safety Management Plan, Continuous Improvement, Environmental Management Plan, Security Plan, Health Plan, Emergency Planning & Response Plan.
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This is an opportunity to join a dynamic team as an Engineer I, Medical Device at a venture backed Medical Device organization, reporting directly to the CTO. The successful candidate will drive key activities throughout the development phases of the combination product as well as transitioning the design to large-volume manufacturing, and facilitate the deliverables to support regulatory filing, product launch, and post market surveillance.
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The Director , Insights + Reporting will be a key part of the Central Analytics & Reporting team that provides critical analyses + information about consumption + release performance to colleagues across US Commercial Partnerships, Global Digital Business and each of Sony Music's US labels.
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Act as the lead clinical pharmacologist on clinical pharmacology study teams to support clinical development: independently lead the design, protocol development, execution, analysis, and reporting of clinical pharmacology studies (e.g., food effect, BA/BE, human ADME, drug interactions, renal and hepatic impairment, etc.
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MINIMUM of 7 years experience within the asset management industry in a data analyst role with a strong understanding of investment functions from fundamental research, investment compliance, risk management, and regulatory reporting.
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Working knowledge of the regulatory environment for utility companies including NERC CIP. Reporting to the CIO, AVANGRID with responsibility for leadership of a staff of over 117 (87 internal and circa 30 external) resources across the enterprise in AVANGRID. Staff located in multiple locations - Orange CT, Rochester NY, Augusta ME, Portland OR, Houston TX.
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Overseeing Bank Secrecy Act (BSA), Anti-Money Laundering (AML), and Office of Foreign Assets Control (OFAC) compliance activities, including monitoring, investigation, and reporting of suspicious activities.
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Responsibilities include but, are not limited to: · Work across functional areas to assess oncology reporting requirements, determine the optimal visualization strategies, and then collect, analyze and present quality improvement data for purposes of Institute-wide program evaluation, management/decision-making, clinical quality improvement, and regulatory compliance.
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The Reporting team empowers sellers to make better decisions for their businesses with data and insights through extensible reporting solutions and discoverable seller experiences. As a Staff Product Manager on the Reporting team, you will be responsible for leading product initiatives from inception through execution.
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Must have 2 years experience with planning, executing, monitoring and reporting of activities for FDA regulatory compliance projects of GxP systems; Performing Root Cause Analysis for deviations from process and agreed metrics; Performing risk management; Working with GxP, GAMP, GDP, 21 CFR Part 11, Annex 11, CSV, CSA, FRA, Risk Based Validation.
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As an Engineer/Analyst with Wiley Edge, you’ll play a vital role in enterprise technology, from algorithmic trading engines to regulatory reporting. How to discuss production support activity at a high level, including ITIL (information technology infrastructure library), monitoring, DevOps, SRE (site reliability engineering), and disaster recovery.
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regulatory reporting jobs Title: compliance specialist Company: Metroplus Health Plan
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