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Proficiency in Warehouse Management Systems (WMS) and Quality Management Systems (QMS). Champion the use of the Quality Management System (QMS) to enhance service offerings and secure new contracts.
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Understand the food safety and quality aspects of the position as indicated on QMS, OJT's and SOP's that apply. Understands principles of QMS, HACCP, and SOP's. Understand the food safety and quality aspects of the position as indicated on QMS, OJT's and SOP's that apply.
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Work with Sourcing team on all pricing, review with Sales lead and maintain margin sheetsPrepare QMS and PLM quotes. Work with Sourcing team on all pricing, review with Sales lead and maintain margin sheetsPrepare QMS and PLM quotes.
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Document control, archive, archival, archivist, doc control, qa, quality assurance, quality associate, quality specialist, quality assurance specialist, gmp, cgmp, gxp, mastercontrol, veeva vault, edms, document management system, pharma, biopharma, medical device, biotech, biotechnology, fda, quality systems, qms, eqms, clinical manufacturing, commercial manufacturing, novel pharmaceutical, novel drug, novel therapeutic.
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Proficiency in electronic QMS software such as Veeva or TrackWise is a plus. Create, document, manage, and/or approve analytical testing-related deviations, CAPAs, and change controls within the Quality Management System (QMS.
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Train employees on Thompson’s QMS including Document and Record Management, Change Management, CAPA, and Internal Audit Programs. Maintain Thompson’s Quality Management System (QMS) for the site to ensure compliance with FDA expectations around Tobacco Product Manufacturing Practices (TPMPs.
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Contributes to the design, development, implementation and evaluation of learning services, education and training courses and material, according to the applicable QMS directives and processes.
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The Quality Specialist I will be responsible for supporting the execution of the overall audit process in support of Innoflight's Quality Management System (QMS). The Quality Specialist I will be responsible for supporting the execution of the overall audit process in support of Innoflight's Quality Management System (QMS.
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The Quality Manager I is responsible for implementation, improvement and execution of the Quality management systems (QMS) and project specific quality program requirements. USACE/NAVFAC/NRC Construction Quality Management certification preferred but not required.
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Support quality and compliance by adhering to all Quality Management Systems (QMS) documentation requirements and establishing/supporting plan(s) to meet/exceed Key Performance Indicators (KPIs) for Quality that support Safety, Compliance, Six Sigma Quality, On-Time Delivery (OTD) and financial objectives.
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Lead Shared Services model providing effective and efficient services to Business Units, Regions, and Functions in the areas of QMS strategy, policy creation, NPSS execution, project delivery/management, and data strategy & delivery, etc.
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Lead the establishment and management of Quality Management Systems (QMS) and EHS programs across multiple locations, aligning strategies with organizational objectives and customer expectations.
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Collaborate with, and provide written requirements to, IT/Digital product selection leads for digital platforms related to manufacturing and operations (e.g. QMS, CMMS, DMS, WMS, CAM, etc.) Collaborate with, and provide written requirements to, IT/Digital product selection leads for digital platforms related to manufacturing and operations (e.g. QMS, CMMS, DMS, WMS, CAM, etc.
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Implement and maintain Electronic Records Program (ERP), Quality Management System (QMS), and applicable Quality Standard Operating Procedures (QSOPs) as directed by Head of QA/QC. HACCP and/or PCQI Certification.
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This role will also be responsible for driving harmonization of the Exact Sciences QMS so that all sites, including critical suppliers, meet the same Quality Standards. The Supplier Quality Engineer will provide support to various operational teams for a variety of functions, with a primary focus on Based on the scope of the assigned area, activities may include process validation, facility validation, test method validation, risk management, change control, exception management, technology transfer, product development, and supplier management.
$67,000 - $109,000Full-timeExpandApply NowActive JobUpdated Yesterday
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