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The QA analyst will be a member of a Data Engineering Scrum team that is delivering solutions focused on using state of the art data and analytics tools including traditional and near real-time data warehousing, big-data, relational and document-based databases using both extract, load, transform (ELT) toolsets as well as REST APIs and FHIR. The ideal candidate will be comfortable with data science platforms with proven experience leveraging DevOps and Test Automation tools.
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Keywords: GMP, GLP, GXP, GCP, batch record management, batch record review, full-process manufacturing, cell therapy, deviations, junior role, maintenance, calibration, FDA, EMA, biopharmaceuticals, quality assurance, QA.
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QA, quality assurance, cell therapy, gene therapy, CAR-T, cell and gene therapy, cell culture, mammalian cell culture, investigation, deviation, CAPA, non conforming, batch record, batch record review, technical writer, quality control, medical, dental, vision, 401k.
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This individual will be primarily responsible for the quality of the FHIR-based content stored within client's Enterprise Analytics Platform, in addition to providing quality assurance oversight of the data pipelines and REST APIs developed by the Data Engineering team.
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This role will work closely with team members in Quality Assurance, Manufacturing, MS&T and Analytical Development. The Analyst I is expected to be an on-site resource at Beam's manufacturing facility in RTP, North Carolina to support project start-up and routine clinical and commercial operations.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Wolfspeed is seeking a proven, hands-on Semiconductor Quality Engineer to proactively lead the Manufacturing Quality function for Wolfspeed silicon carbide wafer manufacturing in the Raleigh/Durham area of North Carolina.
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1 - 3 years (Analyst) / 5+ years (Sr. Analyst) relevant bioanalytical assay experience including flow cytometry and/or ELISA methods. The Senior Quality Control Analyst will be responsible for performing various analytical methods to evaluate the quality of critical in-process samples to support cGMP manufacturing operations across multiple site programs.
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Quality Assurance professional with a BS Biology, Microbiology, Pharmacy, Chemistry, Chemical Engineering (or equivalent) and at least 1-3 years’ experience in the Pharmaceutical Industry. Our esteemed client, a trailblazing global pharmaceutical powerhouse, renowned for their expertise in developing and manufacturing a wide array of world-class pharmaceutical drugs, life-saving vaccines, and innovative animal-health products, is in search of an exceptional Senior QA Specialist to join their dynamic team.
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Flexibility for domestic and international travel· Spanish language fluency is a plusDesired general experiences or exposures through completed classwork or work experience include hydrologic, hydraulic, watershed and/or reservoir model set up, calibration, and assessment/interpretation; spatial, time series, and generalized data collection, organization, quality assurance, and interpretation; and project documentation and report writing.
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Seeks a contractor resource to assist with the development and implementation of NC Families Accessing Services through Technology Curam Application as a Tosca QA Automation Engineer. Requires the services of a Tosca QA Automation Engineer analyzes, creates, and automates tests for the functional and security requirements of applications.
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The American Heart Association has an excellent opportunity for a Sr. Cyber Risk Analyst in our National Center office located in Dallas, TX. (Home-based work available) The Business Technology (BT) Sr. Cyber Risk Analyst is responsible for risk identification and management across the BT department and the overall American Heart Association organization.
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Strata Clean Energy uses the Vista by Viewpoint for the ERP, and the ERP Analyst will need to be an expert in the core ERP as well as any integrated tools. The ERP analyst is responsible for effective provisioning, installation, configuration, operation, and maintenance of ERP systems software and related infrastructure.
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Duke University Health System - Patient Revenue Management Office (PRMO) seeks to hire a Charging Systems IT Analyst who will embrace our mission of Advancing Health Together. Acting as a subjectmatter expert in Charge Router and Charge Review, the analyst will work closely with the Maestro Care teams on system build.
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At least 3-5 years of relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity including at least 3 years of experience in Regulatory CMC and preferably 2 years professional experience in pharmaceutical manufacturing, analytical development, or quality assurance/control or related technical field.
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The Portfolio Analyst should strive to understand the client's operating performance and needs, work to build strong relationships internally and externally, positively impact the borrower's experience with the Venture Bank and generally support the bank's credit risk management efforts.
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assurance analyst qa jobs in Durham, NC
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