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Functionin a lead water process engineer role, as a technical specialist or as a subject matter expert in the areas of conventional water treatment using processes such as coagulation, clarification, softening, media filtration; and advanced water treatment processes such as membrane filtration, reverse osmosis (brackish, seawater), UV/AOP, ozonation, carbon adsorption, and/or distribution system water quality.
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Sr. Validation Engineer to support our Cell Therapy Manufacturing facility located in Memphis, TN. The Sr. Engineer will have the experience to be functional lead responsible for Validation (CQV) deliverables for the facility, utilities, systems and equipment (FUSE.
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Experience working within regulatory standards and requirements such as SOX, HIPAA, GDPR, HITRUST is preferred. The role is for a SSO Engineer on Associates Solution IAM team within Cardinal Health's Global Identity and Access Management organization.
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Responsible for managing the comprehensive validation of Multi Family Models that include Market, Credit and Prepayment Risk, and House Price Appreciation models per business and regulatory requirements.
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Develop and maintain documentation, code repositories, and model validation reports in compliance with regulatory requirements and internal policies. This may include mortgage products and securities, borrower behavior, investment and hedging strategies, residential property valuation, macroeconomic models, including housing prices and interest rate, financial valuation of finance assets and derivatives, economic capital, and stress testing.
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In-depth experience of QC analytical methods and regulatory/pharmacopeia requirements for biologic or cell/gene therapy product testing and method validation for US, EMA and ICH regulations and guidance documents.
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Ensures all appropriate CMC regulatory aspects across teams to support change control requests including transfer of supply within GSK or with a 3rd party are delivered to agreed timelines. Will serve as a key strategic partner representing Global CMC Regulatory on Regulatory Networks and Matrix Teams, providing and overseeing strategic direction and guidance to Biopharmaceutical, Pharma Supply Chain, Clinical Trial Supply, Quality Assurance, and Commercial interfaces on both global project and key strategic business initiatives.
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PURPOSE AND SCOPE OF POSITION (Position Summary): The MES Recipe Engineer and Validation Specialist role will deliver electronic batch record (EBR) configuration and validation in the Emerson Syncade Manufacturing Execution System (MES.
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Senior RF Validation Engineer Onsite-Rockville, MD This is a W2 permanent role As a Senior RF Validation Engineer (7 - 10+ years of experience), you will participate in test plan design and testing of novel RF/microwave and antenna module development for SatCom user terminals.
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Release the emulation/prototyping images to various teams doing functional validation, firmware development and design verification. An experienced Emulation and Prototyping Engineer. + Good knowledge of SoC design methodologies and technologies, with experience in the complete design validation cycle.
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Aid in the design of laboratory and rig-scale experiments for verification and validation of thermal systems. Last Energy is seeking an experienced Thermofluids Engineer for the development of thermal systems components within our comprehensive Power Plant System.
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Are you a passionate, innovative biochemist, virologist, or biomedical engineer ready to tackle one of the biggest challenges in science? Recommend experimental validation strategies for assessing the breadth and potency of vaccine candidates in vitro and in vivo.
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We are seeking a motivated Senior Analyst focusing on AML/BSA, and Fraud Model Validation to join our team. Execute best-practice AML/BSA model validation activities to ensure models are conceptually sound relative to their intended use and performing appropriately.
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Manage electronic (Markit counterparty platform) and paper onboarding process to ensure regulatory compliance; Facilitate ISDA Protocol Adherence Letters and Questionnaires. Supervise and facilitate the regulatory onboarding of new derivatives counterparties in an efficient, compliant, and client-centric manner by coordinating with clients to obtain required onboarding documentation.
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Submitting permit applications via online portals for Client projects to regulatory agencies (DDOT, DOB, DOEE, etc. InterAgency is seeking a full time Regulatory Compliance Specialist to support a large civil infrastructure program in Washington DC, on permitting and regulatory compliance.
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validation engineer regulatory jobs in Silver Spring, MD
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