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Outside of the RWE organization, the VP will work with leaders from other CMAO functions, Biostatistics & Data Management, Global Regulatory Affairs, Clinical Pharmacology / Pharmacometrics, HV&E , Legal/Compliance, Worldwide Medical and Safety, and others to achieve research and business objectives.
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Minimum of 10 years of experience in CMC regulatory affairs within the biotechnology or pharmaceutical industry. We are seeking a highly experienced and strategic CMC Regulatory Affairs professional to join our growing team.
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The Sr. Regulatory Affairs Specialist assists with development, management, and implementation of regulatory strategies to support new and existing Class I and Class II ophthalmic medical devices.
$90,000 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Strong working knowledge of cGMP regulations and Regulatory Agency requirements applicable to biologics and cell therapy manufacturing. Ability to effectively represent the company during interactions with FDA and other regulatory officials, demonstrating credible and substantial QC laboratory expertise.
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Drive operational preparedness for regulatory requirements and collateral management functions. The Trade Operations Manager will have a strong knowledge of fixed income securities, FX, derivatives, collateral management, vendor management, and portfolio system flows.
$175,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Execute necropsy/histology techniques directed by study protocols (regulatory, exploratory and investigative). Perform all assigned routine necropsy and histology tasks in a timely manner and in agreement with the SOP and guidelines in place, from necropsy room preparation to archival of specimens.
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Coordinating with CELA colleagues across the larger worldwide organization on various IP, standards, ethics, privacy, data security, litigation, antitrust, regulatory compliance, and government affairs issues.
$124,800 - $222,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Operate and maintain autoclave machine in accordance with policy and procedures that meet all regulatory requirements. We are leveraging our investment from Washington's largest not-for-profit health plan, Premera Blue Cross, to create a primary care offering that is holistic, seamless, and care centric.
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Please indicate the number of years of experience you have in:a) Water Utility Operationsb) Water Quality Monitoringc) Regulatory Reportingd) Staff Supervision. Ensure regulatory compliance with all applicable water monitoring and reporting requirements.
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License/Certification: Dietician, ADA, Diet Technician, chef, and/or dietary manager - meeting current requirements established by the state regulatory agency. License/Certification: Dietician, ADA, Diet Technician, chef, and/or dietary manager - meeting current requirements established by the state regulatory agency.
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They are looking for a Division Counsel who will supervise and manage all legal affairs within the division, focusing particularly on land acquisition. Division Counsel Responsibilities:Provide legal counsel on land acquisition, zoning, and development.
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JOB DESCRIPTION Job TitlePrincipal Regulatory Affairs SpecialistJob DescriptionPrincipal Regulatory Affairs Specialist- Software & Artificial Intelligence (U.S. Hub Based)The Principal Regulatory Affairs Specialist- SW & AI will shape, lead and execute innovative regulatory strategies to drive innovation within the Philips Innovation and Strategy organization globally.
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The primary focus of the QA Associate role will be to support routine clinical and commercial production to ensure consistent compliance with regulatory and industry expectations. Hands-on experience with batch record review and product disposition.
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The Law Enforcement and National Security (LENS) Policy and Strategy Team in Microsoft's Privacy, Safety, and Regulatory Affairs (PSRA) organization has an opening for an experienced attorney to join our team at our headquarters in Redmond, WA or one of our U.S. hubs, including Reston, VA, or Mountain View, CA.
$141,800 - $248,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Full understanding of GCP, GLP and GMP regulations and regulatory compliance guidelines. Perform audits on clinical investigator sites, vendors, processes, systems, and study documents to assure quality assurance compliance with regard to internal procedures as well as regulatory guidelines.
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regulatory affairs jobs Title: regulatory affairs Company: Abbott Laboratories in Woodinville, WA
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