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The Manufacturing Specialist will support cGMP activities at the Durham North Carolina Site. The Manufacturing Specialist will have responsibility to assure initiatives related to production readiness and compliance are optimized and executed appropriately in the areas of GMP production.
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The Quality Assurance Specialist III -Medical Device will provide advanced-level, hands-on support from a regulated systems perspective in a GxP laboratory services and kitting production environment.
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The Final Product Specialist is responsible for review of documentation completed for production, testing, labeling and shipping veterinary vaccine products. QA Final Product Release Specialist.
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Required Skills Experience with entire software development life cycle and test cycles Experience with writing effective test cases and test scripts Experience with gathering, documenting and testing of business requirements Experience with gathering, documenting and testing functional requirements Experience in change management Experience with Agile Development Methodology Experience using the Test Manager Experience with Team Foundation Server (TFS/DevOps)QA Specialist/Tester.
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Mortgage Connect is looking for a sharp and enthusiastic Production Quality Assurance Specialist familiar with the printers and inserters currently utilized by the Mortgage Connect Document Solutions Automated Document Factory (ADF.
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The QAOperations Documentation Specialist position provides documentation supportaligned with commercial and development production. QA Operations Documentation Specialist.
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Assist Quality Assurance Specialist III in the management of eQMS.Assist in records control of QMS and production documentation. Assist Quality Assurance Specialist III in maintaining the Quality Records and production documentation within eQMS. Assist in additional duties delegated from Quality Assurance Specialist III and Quality Lead. Education (describe the minimum requirements for education for the position)Requires a bachelor’s degree in a scientific discipline or equivalent Experience (describe previous minimum experience required for the position.
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Establishes regular meetings to communicate quality metrics and present potential focus areas to QA Manager and QC/Production Managers/Supervisors as necessary. Performs in-process verifications for reagent volume and tube vacuum throughout the production run.
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The QA Compliance Specialist is responsible for maintaining and/or managing quality systems, processes, and documentation to ensure compliance with current Good Manufacturing Practices (cGMPs.
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A good understanding of related functional areas of a pharmaceutical company (e,g, analytical, clinical trials, production, QA, regulatory affairs). The Senior Application Specialist is an experienced technical professional that provides support to IFF Pharma Solutions products and applications in North America.
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The Quality Control (QC) Inspector will report to the Manager, QA Inventory, Testing and Distribution and will support the execution of the Quality Assurance & Compliance (QA&C) program by executing QC inspections as a member of the "front-line" Cultivation or Production process.
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Assist Builds and deploying Web Applications in a clustered and load balanced N-Tier infrastructure into staging (QA) and production environments. LabCorp is seeking a IT Project Specialist.
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Work closely with engineering team to assist them to deploy these applications in all Environments controlled by engineering team (Software Test, Performance Test, Staging and Production). Communicated all key project plans, commitments, and changes including requirements, QA plans, schedule, and scope changes.
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The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing Organizations (CMOs.
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We have an immediate opening for an Entry Level CAD Tech + Quality Assurance Specialist. This position will train in both the CAD and QA departments under Operations to work a hybrid role.
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