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This includes overseeing quality assurance engineering, in-process and final inspection, supplier/vendor QA engineering, and/or process excellence programs for SJI and their natural gas utilities.
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The New Jersey Judiciary, Essex Vicinage is seeking a conscientious, highly motivated individual to work under the direction of the Court Executive 2B (Probation Division Manager and/or Court Executive 1b (Assistant Probation Division Manager) as the Quality Assurance Specialist.
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Center 1 (19052), United States of America, McLean, VirginiaPrincipal Associate Cyber Risk & Analysis, Technology Audit (Hybrid)Capital One’s Audit function is a dedicated group of professionals focused on delivering top-quality assurance services to the organization’s Audit Committee.
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Knowledge of cGMP, GxP, GAMP, and SDLC regulations, including 21CFR part 11 electronic records and electronic signatures, and good documentation practices with the ALCOA+ principles of data integrity, risk-based approaches to validation, Computer Software Assurance (CSA) principles.
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Familiar with the development of CSV documentation (Validation Plans, Requirements, Design / Configuration Specifications, Test Scripts [IQ/OQ/PQ/UAT], Summary Reports, Trace Matrices, SOPs) Experience with MES infrastructure, ALM and Veeva document/change management systems and middleware WebMethods.
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Clinical supplies, biologics, vaccines, electronic batch record review, batch record, cGMP, SOPs, specifications, labeling, regulatory submissions, SAP, Trackwise, Midas, Veeva, QMAS, QA, Quality Assurance.
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Immediate need for a talented Manufacturing Systems Validation Specialist. Minimum of 2+ years relevant work experience required preferably in a pharmaceutical manufacturing environment. Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation.
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Ability to work extended hours or a modified work schedule to assist manufacturing operations support model, including 12x7 on-call support rotation. Please review the job description below and contact me ASAP if you are interested.
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Responsible for the Health & Safety segment support as Health & Safety Single Point of Contact (HS-SPOC), strategic planning, deployment, compliance, loss prevention & incident investigation, and training within the assigned Zone. Health & Safety includes all safety disciplines, such as environment, health and safety, food safety, and product quality assurance.
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IRT management activities including IRT Alert management and UAT activities. The Sr. Clinical Supply Operations Specialist provides support to the Clinical Drug Supply & Logistics group in the Investigational Product (IP) distribution process, ancillary supplies process and comparator procurement process, for one or more molecules across multiple Therapeutic areas; supporting highly complex studies as well as long-term departmental and cross-functional projects and on-going continuous improvement initiatives.
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Our focus on combatting climate change through clean energy technology, our new net zero climate vision for 2030 and enhanced commitment to diversity, equity and inclusion; and supporting the communities we serve make this a particularly exciting time to join PSEG. Job SummaryThis position is part of PSE&G's Centralized Services Quality Control and Assurance group supporting Gas Operations.
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Uses testing equipment to test samples of products to ensure they are in compliance with specifications and document results in required logbooks and/or batch records; reporting any deviations in results to the Quality Assurance Manager.
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In this role, you will provide technical assistance and apply skills related to project management, engineering design, slope stability, field investigations, construction quality assurance, and permitting, for solid waste infrastructure and aggregate mining projects and systems in both the public and private sectors.
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Responsibilities include management of the Authority’s NJDEP-certified laboratory including supervision of laboratory personnel, scheduling and coordination of all permit and process control-related sampling and analyses, quality assurance and quality control checks at required frequencies, instrument calibration and maintenance, review, and compilation of all data collected, and coordinating sampling of dischargers to the HSA system with the IPP Manager.
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The ideal candidate will have a solid background in software quality assurance, with expertise in TOSCA automation testing. Proven experience as a QA Lead with a focus on TOSCA automation. The ideal candidate will have a solid background in software quality assurance, with expertise in TOSCA automation testing.
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uat assurance jobs in Summit, NJ
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