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Maintain all x-ray equipment, including calibration, QA/QC procedures, and record keeping in accordance with current policy and procedures. X-ray Technician Duties. Maintain all x-ray equipment, including calibration, QA/QC procedures, and record keeping in accordance with current policy and procedures.
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The eCommerce Manager, QA Engineering will report to the Director of Quality Engineering and lead a team of highly motivated quality engineers. Lead the implementation and rollout of QE processes, aligning them with business/customer needs; Lead UAT sessions with Business and communicate business risks and mitigation plans based on testing outcomes.
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Ability to work independently and provide guidance and leadership to junior team or project members, with strict adherence to QA/QC.Proficiency with technical writing, office automation, discipline-specific design software (i.e., MicroStation, AutoCAD, Civil 3D, ArcGIS, InRoads, Geopak, GeoSlope, ANSYS, STADD, HEC-RAS, HEC-HMS), technology, math principles, physics, predictive models, spreadsheets, and tools.
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Collaborate with UX / UI design, engineering, and QA staff to implement design-to-code workflows, to facilitate the rapid prototyping, testing, and continuous delivery of robust, engaging user experiences.
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As a QA Director, you will own skills development, quality metrics progression, and refining quality strategies for Turtle Rock Studios QA team as well as be responsible for evaluation, negotiating with and managing a network of QA vendors for upcoming projects.
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The X Ray Limited Scope & Medical Support Specialist performs routine x-ray, medical, and testing procedures under direct supervision of the treating clinician as well as supports in other areas of the facility as needed including registration and referral management.
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At least 7 years of consulting experience that involves oversight, QA/QC, technical writing, advanced survey design, impact assessment and multi-media permitting. Contribute to preparing technical documents and associated management plans in compliance with state and federal requirements, serving in roles ranging from lead technical expert to QA/QC.
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Knowledge of basic GMP and QA/QC in the food, nutraceutical or pharmaceutical industry. Knowledge of basic GMP and QA/QC in the food, nutraceutical or pharmaceutical industry. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.
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8+ years continuous experience in advanced software deployment in the manufacturing industry, specifically in the areas of Process Planning (PP), Manufacturing Execution (MES), Quality Assurance (QA), Supplier Quality (SQA) and Maintenance and Overhaul (MRO.
$140,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Continually assess the Supplier Management and QA Management system and SOP's for continual improvement. In countries where vaccines are less available, or other requirements exist, we may institute alternate measures that optimize patient safety and healthcare provider safety, which may include regular COVID testing or specific masking requirements.
$101,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Acra Lending is hiring for an IT DATA QA ANALYST! Experience with Domo, SSRS, PowerBI, SQL, Tableau, or other dashboard and/or reporting platforms, a plus. Monitor, collect and assemble data from multiple sources to identify trends and provide strategic recommendations and actionable data from the data warehouse and reporting systems; including but not limited to Domo, BytePro, Finastra Servicing Director, MS SQL server and AWS.
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The Senior QA/RA Specialist I is responsible for supporting the Senior Director of QA/RA in leading the planning, maintenance and improvement of compliance with Quality Management Systems (QMS) processes relevant to Agendia, Inc., which helps ensure compliance with regulatory requirements and standards that are applicable, such as FDA, CAP, CLIA, ISO.
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Contribute to preparing technical documents and associated management plans in compliance with state and federal requirements, serving in roles ranging from lead technical expert to QA/QC.Achieve client’s expectations for scope, budget, schedule, and quality.
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Advanced working knowledge of QA principles including Quality Risk Management (QRM), Critical Thinking, and Quality by Design (QbD). Minimum of four (4) years of experience in clinical research and/or GCP related QA environment including auditing and/or external inspections (e.g., BIMO.
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About this position at Lightspeed LA Lightspeed LA is seeking a QA Tester earnest about working on a new project in Irvine California for our QA Tester II position. Pluses QA testing experience with games, especially consoles, and 1st party certification testing.
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