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Assist in method development and validation for LC-MS/MS, GC/MS, and Immunoassay at the direction of the QA/QC Supervisor - 30% of the time spent on this task. Must gather and copy all PT data in a timely manner, promptly alerting the QA/QC supervisor of any issues with data that may need a sample to be repeated.
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Ensures city, county, state, and federal regulations relating to the QA/QC laboratory are met at all times. Participates in the safety program for the QA/QC laboratory.
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Laboratory training internship, plus Medical Technologist (MT), Histotechnologist (HT) or Cytotechnologist (CT) by American Society. Anatomic Pathology Manager, requires cytotechnologist licensure in State of Florida.
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Enter interpretations into the laboratory information system, appropriately triage cases requiring further evaluation either by a QC technologist or pathologist, and issue a report for Pap tests that do not require further review.
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Documents and brings to the attention of the Laboratory Supervisor, Manager or Director any errors, omissions or discrepancies in QC. Compiles QA data and prepares reports as directed by the Laboratory Supervisor, Manager or Director.
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The QA/QC Supervisor is responsible for the implementation of the RES Quality Management System and the execution of the Quality Control Processes and Procedures for the Project Site Construction Team. In conjunction with the HSQE Quality Manager, the QA/QC Supervisor develops and maintains the Construction Quality Plan and the Inspection Test Plan (ITP) throughout the duration of their assigned project; the position is 100% site based.
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Performs pre-analytical, analytical and post-analytical phase testing of all complexities as defined by Clinical Laboratory Improvement Act/Amendment (CLIA) to include specialized tests and analysis in one or more areas of clinical laboratory such as Hematology, Microbiology, Clinical Chemistry, Urinalysis, Immunohematology, Serology, Parasitology and chemical and morphological examinations to obtain data for use in diagnosis and recording laboratory test results.
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Pattern IIIMaster’s degree from school of cytotechnology accredited by the Committee on Allied Health Education and Accreditation or other organization approved by HHSAND:Board eligible or less than three years laboratory training or experience as a cytotechnologist in a high complexity laboratory.
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Install, Configure & Monitor the performance of the Windows Server environment used to host the HP Performance Center (PC) & Load Runner (LR) & JMeter, Application Life Cycle Management (ALM) & Quality Center (QC) and Unified Functional Tester (UFT) & Quick Test Pro (QTP) services, Install, configure and manage necessary License Servers and Licenses so each HP service runs efficiently for our customer agencies across the NYS Enterprise.
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Reporting to the Vice President of Video Distribution & Content Operations and working closely with the Senior Manager, Content Metadata & QA, Senior Manager, Content QC, and Manager, Content Operations, you'll oversee the subject matter expert teams for video metadata display, syndication, and governance.
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The QA/QC Supervisor exhibits strong knowledge of the implementation of a Quality Assurance and Quality Control program as well as the management of Quality documents and the creation of Quality Records on construction sites.
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The Cytotechnologist provides professional services, including interpretation of Pap tests, slide preparations, proficiency testing, quality control and other functions and is a key member of our laboratory team, helping Axia to provide full scope of services to Axia Women’s Health patients.
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Quality Assurance/Quality Management (QA/QC) support activities for the TSL; and. GST is actively seeking a Configuration Management (CM) Specialist in support of our Department of Homeland Security (DHS) Science and Technology Directorate (S&T) Transportation Security Laboratory (TSL) customer working full-time at the FAA Technical Center at the Atlantic City Airport.
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In collaboration with the Supplier Quality lead, develop and manage the GCP/GLP/GVP internal and external audit programs to meet all US, European and global Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Pharmacovigilance (GVP) requirements.
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Follow strict quality control procedures established through the QA/QC supervisor and adhere to California Environmental Protection Agency and United States Environmental Protection Agency's analytical procedures.
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laboratory cytotechnologist qa qc jobs Company: Northwell Health
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