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Represents the City before the PUCT, TxRRC, ERCOT, TCEQ, and the TWDB and provides strategic and tactical external energy and environmental advocacy in regulatory proceedings to ensure equitable access to clean, affordable, and reliable energy resources, to support customer demands, and to set the groundwork for future business growth.
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You will join the Regulatory Operations Legal Team (Reg Ops Legal)which provides cross line of business legal support to the Consumer and Community Bank (CCB), which includes Auto Finance, Home Lending, Business Banking, Card Services, Consumer Banking, JPMorgan Wealth Management and associated operations.
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A scientific degree with directly relevant professional experience in small molecule development, global CMC regulatory affairs and CMC technical areas of at least 16 years with a BA/BS or 14 years with an MA/MS, PhD, PharmD, or MD.
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Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages.
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The purpose of the Sr. Director role in Global Regulatory Affairs (GRA) - Drug Delivery and Digital Health provides strategic, tactical, and operational direction to expedite Lilly's drug/device combination products in development.
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Provide direction, technical support and a high level of expertise to the implementation of Process Safety Management (PSM) policies, standards and best practices; work with the site to ensure compliance with government regulatory requirements, applicable international standards, internal SABIC Policies/Standards and Responsible Care codes.
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Global Regulatory Policy Manager – Liquidity covers a number of key aspects of prudential interpretation, including risk weighted assets (RWAs), capital resources, and the leverage ratio, across a full range of risk areas e.g. credit risk, counterparty credit risk, liquidity risk, securitisation, market risk, etc.
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Minimum 7-10 years experience interpreting and implementing financial services regulatory programs, preferably related to anti-money laundering and/or enterprise risk management. Bank Secrecy Act (BSA), Communication, Compliance Monitoring, Compliance Programs, Compliance Requirements, Customer Onboarding, Management Reporting, Regulatory Compliance, Regulatory Compliance Management, Regulatory Reporting, Risk Management, Sanctions Screening, Suspicious Activity Reporting (SAR.
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Define and implement a process for reporting to management the status of BSA/AML/OFAC/CTR regulatory compliance, including the details of any identified BSA/AML/OFAC/CTR issues and the corrective action taken.
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Legal and Regulatory Compliance: Ensure KAZI FM's adherence to all legal and regulatory requirements related to radio broadcasting. Knowledge of legal and regulatory requirements related to radio broadcasting is a plus.
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Etc),hazard communication, control of change, hazardous waste management, reporting site key performance factors, Green House Gas data, chemical management systems and programs, personal protective equipment, dangerous goods – hazardous materials management, emergency preparedness, regulatory reporting and data collection.
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Minimum of 5 years of experience as a Developer/Business Systems Analyst with a focus on QMS in the medical device industry, including expertise in Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
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A minimum of 6-10 years’ experience in product stewardship, regulatory affairs, compliance, chemical consultancy, and/or risk assessment. The ideal candidate will have experience in chemical and environmental regulatory compliance, packaging regulations, product stewardship and industrial risk management in the medical device or manufacturing industries.
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In addition, review and approve CTL assay development and validation reports, relevant sections of clinical documents pertaining to AAV and RNA analytical testing and documentation for submission to regulatory agencies.
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In collaboration with the Federal Policy Director, develop and implement a comprehensive federal regulatory affairs plan in support of the policy priorities of the Federal Policy Office and to define short- and long-term goals and objectives related to WE ACT’s policy impact.
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regulatory job Title: sr director Company: Jazz Pharmaceuticals
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