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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 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. Responsible for project management, production line trouble shooting, administering budgeting, design, installation, qualification, and commissioning of new/modified process systems.
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Minimum of 10 years’ experience in GMP QC/QA/Quality Systems, Microbiology or Analytical Development in biopharma/pharmaceutical industry. Create, document, manage, and/or approve analytical testing-related deviations, CAPAs, and change controls within the Quality Management System (QMS.
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Candidate will maintain a Quality Management System for Thompson in an FDA regulated environment for tobacco cleaning work on-site at a tobacco manufacturing facility in Richmond, VA. The Quality Systems Specialist will manage all required Quality System documentation including a site Quality Manual, Quality System training for employees, Records Retention procedures, TPMP training, FDA protocols, Work Instructions and other required quality system documents.
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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). This position requires a high amount of accountability to be an effective Quality Specialist.
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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.
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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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Direct PM and engineering team supporting the QMS/Tool simplification programs as part of the overall Quality Strategy landscape. Includes development and maintenance of quality policies, QMS infrastructure and select QMS capability excellence to enable the use of processes and tools by BU, Functions, and Regions.
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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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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.
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Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
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Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
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For example, Change controls and QMS sub-systems ownership. 3 to 5 years previous experience within Quality operations/ Compliance or supporting Supply Chain or Operations role within a Pharmaceutical Company.
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Responsible for all aspects of quality systems and staff, QMS conformation to AS9100 standards, internal and external audits, process optimization, cost reductions and continuous improvement.
$80,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
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