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General laboratory operations (ordering supplies, preparing buffers/mobile phase/culture media, operating laboratory equipment, participation in quality and safety assessments, sample receipt, notebook data authoring/review/integrity following good documentation practices.
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Direct observations of performance of routine and quality control procedures including, as applicable, donor suitability, sample handling, processing, testing, labeling, and instrument preventive maintenance.
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Perform QA in-process inspections for each department/line once per shift by checking the following: production paperwork, retain sample, code date/lot number/best by date, weight check documentation, metal detection documentation, label, color code, department cleanliness employee GMP practice and checking for any potential allergen cross-contamination.
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The QA Specialist is responsible for monitoring products and employee practices on the manufacturing floor to insure the safety and quality of products manufactured by Georgia Nut Company. Perform changeover validation on production lines and perform clean equipment/ATP swabbing on equipment after sanitation policy 6615.
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The CRC is a combined inpatient-outpatient unit and encompasses a total of 10,900 square feet, comprising inpatient beds, outpatient exam rooms, a sample processing lab, a metabolic kitchen, and conference and office space.
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An approved writing sample exemplifying clinical documentation will be required for. responsible for all client-related services and documentation. Job Location: Greenville Residential Reentry Center - Greenville, SC.
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Sample preparation and documentation of samples pending shipment and testing at clinical lab. Daily mixing and documentation of chemical disinfectants for C2C units and other chemicals required for routine daily cleaning.
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An integral part of the Field Marketing Juice Crews role is to sample & educate consumers, while creating a memorable experience that will build brand awareness and drive brand loyalty. Submission & approval of activation reports within specified, required time frame that includes photos, activation results, shift documentation & consumer feedback.
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The Suja Juice Crew is a dynamic team of active, outgoing, and knowledgeable individuals, who are passionate about spreading the Suja Love. They live by way of Suja; leading healthy & active lifestyles and are eager to encourage others to live a long, beautiful life by way of conscious nutrition.
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Completing internal controls documentation, risk assessment, testing and random sample generation for internal and external audit engagements. Handling the reporting phases of engagements, including completing reporting documentation according to firm standards, GAAS, and best practices.
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Assists in implementation of a laboratory quality assurance program, including instrumentation maintenance and calibration, control sample testing and review, and all documentation required of a sound program.
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Under direct supervision the Quality Technician I assure the Quality of Laird processes and products by performing audits, inspections, tests, supports defect investigation and analysis, first article sample submission (AS9102) and maintains high detail-oriented documentation process for all internal processes as well as for Source Inspection Items that need to be presented to Customer.
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Manage the plant laboratory; supervise, train, and certify operators; manage the sampling and testing of finished goods delivered; maintain test equipment, QA/QC documentation, records, and sample archives.
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The contractor shall maintain a Top Secret security clearance for security of sensitive key supporting documents and have experience in responding to sample and PBC request for documentation in a SOF environment.
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Other responsibilities include cGMP documentation, sample login, data review, instrument maintenance, and other tasks assigned by management. Degree must be within a relevant field: (Biology, Biochemistry, Chemistry, or Toxicology) Masters plus 1 year of relevant experience, or Bachelors plus 3-4 years of relevant experience, No degree requires 7 years of relevant experience.
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