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Government and Community Relations division of the County Executive Office (CEO) within the Office of Legislative Affairs, the Grants Administration Analyst reports to the Legislative Affairs Director.
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The Senior Sustainability Analyst will contribute to key activities in measuring our environmental impacts as part of the Global Sustainability Team. This role will collect, aggregate and analyze data to measure the environmental impacts and progress toward goals across our materials and products, and help the team prepare for emerging ESG regulatory compliance.
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People: We have transitioned thousands of officers into successful careers in law enforcement, government services, foreign affairs and many more. About Inter-Con Security Passion: Joining the Inter-Con family is an opportunity for growth in an environment that truly cares for its employees.
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Assist with projects involving SPCC, stormwater, NPDES, hazardous waste, hazardous materials, EMS, air quality and other environmental regulatory compliance services including regulatory research, compliance planning and auditing, creating spreadsheets, and compiling and writing reports and other documents.
$70,000 - $84,000 a yearExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Administrator - National General Affairs position oversees travel policy compliance by reviewing requests, arranging travel, and ensuring reimbursement adherence. Multitasking: General affairs personnel often have to juggle multiple tasks simultaneously, being able to switch between tasks efficiently is important Required.
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Knowledge of legal and regulatory requirements related to non-profit organizations. Previous experience as a healthcare or public health educator. Knowledge of legal and regulatory requirements related to non-profit organizations.
$140,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Holds certifications or approvals from key regulatory agencies such as the U.S. Army Corps of Engineers, U.S. Fish and Wildlife Service, and state agencies required to perform and/or oversee surveys, delineations, and other discipline specific requirements.
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Participates in ongoing training to maintain current knowledge of BSA/AML and OFAC new and emerging money laundering and financial crime typologies and risks as well as regulatory requirements.
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Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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Builds and maintains relationships with relevant stakeholders including Regulatory Affairs functional areas, Precision Medicine, Medical Affairs and Commercial organizations. The Manager, Regulatory Affairs In Vitro Diagnostics and Companion Diagnostics works with internal and external partners to develop and implement global regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives.
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The Software Test Manager is responsible for supervising the software test engineering team, establishing policies and procedures for design verification and validation, planning and execution of design verification and validation, designing and leading the building of design verification hardware/software, test equipment and products, and developing test procedures based on product performance requirements, customer expectations, and regulatory standards.
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Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients.
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In addition, the Clinical Affairs Program Manager will perform annual activities associated with Post Market Surveillance (PMS) program, including but not limited to, preparing and writing plans, reports and Post Market Clinical Follow-up (PMCF.
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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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The Aircraft Cabin Agent is responsible for cleaning and conducting security searches on designated aircraft according to Company, Client, and Regulatory policies, specifications, and standards.
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regulatory affairs jobs Title: sr regulatory associate in Irvine, CA
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