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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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Perform daily GMP Quality Control laboratory testing activities. 3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus.
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The QAU will support the comparable GMP production activities related to GLP toxicology lot production and technical transfer activities as it relates to clinical batch release testing conducted at GTP to support the clinical CMO. The QAU will also provide Quality Assurance support to the research-based portion of the GTP, in terms of SOP management, training, document management and archiving, and audit support.
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Experience Designing and implementing software-defined network (SDN) architectures such as Cisco Application Centric Infrastructure (ACI), VMware NSX, and Cisco Catalyst (DNA) Center, (Assurance/SWIM & Provisioning), SD Access and SD WAN.
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Experience in quality assurance, and food safety management systems, meat and poultry HACCP and SQF Practitioner. Experience in quality assurance, and food safety management systems, meat and poultry HACCP and SQF Practitioner certification is desired.
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Quality Assurance Automation Test Engineer Philadelphia, PA Posted: 5/17/2024 Job Description Job ID#: 57116. Bachelor's degree with a concentration in Information Technology or Computer Science or equivalent significant experience in information technology and software testing is required.
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Shift Sunday through Thursday Essential Functions and Responsibilities Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulationsPerform data analysis and final result reporting to support product lot release with adherence to turnaround times.
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Experience: Minimum 2 years of post-doctoral research training and applicable experience to include serological testing, solid-phase assays, molecular biology techniques including NGS, and flow cytometry technologies as applicable to solid organ testing or equivalent combination of education and related experience required.
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Assure that proper document control, quality assurance documentation and construction project records are kept. Job Description ResponsibilitiesTo perform quality control construction observations for various highway roadway and bridge construction, general site work, maintenance and protection of traffic, drainage, earthwork, paving, concrete work, reinforcement steel placement, utility relocation work, coordination, and safety.
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Quality Assurance/Quality Management (QA/QC) support activities for the TSL; and. Working in a Laboratory Environment the Configuration Management (CM) Specialist will be capable of the following: Performing planning and scheduling, progress reporting, cost control, organization, technical risk analysis, financial planning, acquisitions, quality assurance, and quality control on all submitted deliverables.
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San Francisco, California (Hybrid On-Site): $291,100 - $332,300 for Director, Software Engineering. New York City (Hybrid On-Site): $274,800 - $313,600 for Director, Software Engineering.
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Expertise in the conception, formulation, optimization, automation, processing, characterization and manufacture of a unique silicone polymer composition of a specialty medical device including analytical chemical testing including gas and liquid chromatography, gel permeation chromatography (SEC), UV/Vis, FTIR, viscosity testing.
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This role will assess business processes and identify areas of application for RPA technologies, as well as architect, design, develop, and deploy software robots, or bots, to work alongside humans to enhance business process efficiency.
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We’re building the world’s most advanced healthcare platform from the ground up, combining hardware, software and doctors under one roof. Use clinical skills for specimen collection, point-of-care testing, clinical procedures.
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Focused on data modeling, data quality, data integration and data governance. Familiar with software development methodologies Agile/Scrum/Kanban and understanding of enterprise project lifecycle.
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quality assurance software testing jobs Title: quality assurance intern in Collingswood, NJ
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