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You have experience with risk assessment methodologies, regulatory compliance requirements (e.g., GDPR, SOX, PCI DSS), and industry standards (e.g., NIST, ISO). You have extensive knowledge of risk management, audit & regulatory compliance principles, practices, policies and procedures, with experience writing controls and mapping controls to regulatory requirements.
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Manage the bioanalytical assay transfer/validation, quality and conduct at external bioanalytical vendors and ensuring regulatory compliance. + Working knowledge of bioanalytical method validation and sample analysis regulatory guidelines in all regions (ICH, FDA, EMA, PMDA.
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This individual will work collaboratively with members of all departments within the company, including but not limited to Offshore Wind Development, Onshore Development, Origination, Transmission, Regulatory, and Environmental Compliance & Strategy.
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This position is ideal for self-starters with bank auditor experience, regulatory examiner experience or banking industry experience within risk management. Audit experience within Banking, Accounting / Consulting, Regulatory Agencies, or Financial InstitutionsCertified Internal Auditor (CIA) or willing to obtainAdditional Certifications:CRCM, CPA.
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Experience with Information/Technology Risk Management, Supply Chain Risk Management, Third Party Risk Management, and/or Global Regulatory Compliance. These critical initiatives require strong leadership to ensure compliance with policies, standards, regulatory requirements, and best practices.
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This role will lend support and serve as a back up to the senior fee reconciliation specialist of the team and help ensure that the firm remains compliant with exchange regulatory requirement related to exchange fees and to operate efficiently and effectively in the market.
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The Cardiac Sonographer reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards.
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Exposure working with regulatory/listing agencies such as UL, FM, CSA, and CE mark One (1) or more years of experience in the use of PTC Windchill. Demonstrate proficiency in tools such as Microsoft suite of tools, Pro-E/CREO, PDMLink, Configured product Articulate and skillful at creating information, written or otherwise Exhibits good analytical skills with ability to organize, implement projects to detailed timelines and budgets Familiarity with the most current Product Lifecycle Management systems and methods, CAD systems and tools, project management, content management systems, and the communication and interaction between IT systems.
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Works closely with our Middle Office executing on regulatory and audit deliverablesCollaborates with Senior Partners helping with business continuity planning/testing, resiliency and RCSA analyses.
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With a suite of highly customizable tools, DASH designs and delivers intelligent, high performance solutions in four product categories: Trading Technologies, Execution Services, Analytics and Regulatory Technologies.
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We assist companies and non-profit organizations in delivering benefits to their employees.
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Job Description SummaryUnder the direction of the Manager of Regulatory Accounting, and adhering to established policies and procedures, the Grant Accountant will perform a variety of professional tasks related to federal grant accounting such as providing financial management for federal awards, posting journal entries, preparing various reports and reconciliations, while ensuring financial compliance with federal regulations.
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Lead the organization's SOX compliance efforts, ensuring adherence to regulatory requirements and internal policies. Stay abreast of emerging risks and regulatory changes impacting SOX compliance, and proactively address any implications for the organization.
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Collaborate with Regulatory Affairs and Pharmacovigilance in the development of product labeling and periodic safety reports, as applicable. Purpose and Scope:The Medical Lead, Oncology, MUS (Medical Affairs-United States), is accountable for the development and execution of medical and scientific strategies for one or more products within the Therapeutic Area (TA.
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Ensure compliance with national and international regulatory requirements, architectures comply with key standards (3GPP, GSMA, ITU, RFCs), and adherence to industry standards and best practices.
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regulatory job Title: sr regulatory affairs Company: Modis in Northfield, IL
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