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Perform QA/QC duties as assigned. Enter data in laboratory information systems (LIS). Perform QA/QC duties as assigned. One (1) year full-time experience in a technical or clinical laboratory department.
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Site: Ascension St. Vincent 3700 Washington Ave. Evansville, IN. Schedule: Full-time/Evenings/ Monday-Friday 2:00pm - 10:30pm (Rotational Weekends) Clean, organize and maintain work area,glasswareand laboratory equipment (e.g., refrigerators, freezers and supply cabinets, asneeded.
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The Analyst will support nomination QA/QC reviews. While supporting the Screening & Vetting mission the analyst will be responsible for screening and vetting individuals traveling to the US by reviewing non-immigrant and immigrant Visa applicants against TIDE and other IC databases.
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Responsibilities will include using appropriate tools and analytic tradecraft to evaluate, analyze, and integrate relevant identity information to reveal foreign traveler links to terrorism for the State Department adjudication and watch listing purposes.
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Conducts wide variety of laboratory procedures; performs challenging and detail orientated lab work in QC/QA lab. With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process.
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This position will serve as the primary point of contact for Plant QA/QC laboratories, addressing requests for instrumentation support, special sample analyses, and troubleshooting issues.
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Assist review of Quality Plan, Inspection & Test Plan (ITP) and Quality Procedures and all pertained QA/QC documentation prior to commencement of any fabrication / construction work •Able to schedule and monitor ongoing NDE activities •Able to monitor that the correct materials are being used.
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Keeping the laboratory in compliance with QA/QC initiatives, DOT, AMRL, CCRL, and AASHTO accreditation requirements. Working in a laboratory that tests both geotechnical and CMT materials.
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Review QC/QA test results to Waste profile Sheet to determine if results match profile. File, electronically, the completed QC/QA document. Complete and submit QC/QA documents to Operations.
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Adhere to project, department, and corporate QA/QC procedures as appropriate. Knowledge and familiarity of the National Bridge Inspection Standards, AASHTO Manual for Bridge Evaluation, and the Bridge Inspector's Reference Manual.
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IT Tech Ops team needs onsite Lab Support Specialists for the MVP01 (Oceanside) and RDMC (Santa Monica) QC Labs. The scope includes efficient and reliable operation of internal desktop lab systems and will handle tactical matters such as service requests as well as when working on larger projects.
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Skills and/or Training Desired:Experience in QC, QA or inspection, analytical laboratory experience using HPLC, TLC, GC, ICP/MS, FTIR, UV-Vis spectrophotometric, microbiological, and general analytical laboratory techniques.
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The QA Specialist I will play an essential role in helping CuriRx transition from a CRO to a CRDMO, bringing their knowledge of quality systems to support the growing QA/QC team. Masters degree in chemistry, biochemistry, life sciences, a related field, or a professional certification such as ASQ or Six Sigma Green Belt or higher.
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Strong awareness of industry recommended practices, OSHA requirements, equipment, and QA/QC. Assist in the implementation of QA/QC programs. Strong awareness of industry recommended practices, OSHA requirements, equipment, and QA/QC.
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Lab Assistant II - Chantilly, VA - Thursday to Monday 10:00PM - 6:30AM. Perform specimen receiving, labeling,handlingand preparation. Assist with pre-analytical preparation of specimens (e.g.,printing labels,uncap/cap specimen tubes,aliquot specimens,prepare racks, worklists, enter/scanspecimensand load automated instruments.
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