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Pen/Pen Scripting, Python, UNIX/Linux, PL/SQL, Microservices, JIRA, Lean Kit, TDP, TOAD, SQL Developer, Rally, Selenium, Soap UI, Postman, XML, Quality Center, and Shell scripting. REQUIRES: Master’s or equivalent in Computer Science/Applications, Information Technology, Business Management/Administration or Electronics Engineering + 1 year experience as Software Quality Engineer, Software Quality Assurance Analyst, Test Engineer, Quality/Product Test Professional or related.
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Ensures compliance, quality and suitability of all excavation and recovery of subsurface UXO; construction of UXO-related protective works; the location of surface UXO by visual means; transporting and storing UXO assuring compliance with Federal, state, and local laws.
$80,000 - $88,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC. Hands-on experience with designing and implementing GMP Quality Systems.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. A background of pharmaceutical manufacturing or quality control/quality assurance is a plus.
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Job Title: Lead - Quality Assurance. Gather application's business requirements and specifications for developing architecture pattern, formulating test plan & strategies, test analysis, test design, test cases, development & maintenance of database using Azure DevOps, IBM Rational and Collibra Data Governance center, SharePoint, Data Modeling, & Oracle SQL Developer.
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Knowledge of quality systems (GxP, ISO, Lean, TPS, etc.) Then consider joining us as a Quality and Safety Manager in Piscataway, New Jersey! You will be responsible for the overall quality and safety for the full environment of our new distribution center.
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Comprehensive knowledge of global GMP and regulatory requirements for biotechnology, cell and gene therapy products and Quality by Design approaches. This individual will be responsible for Quality oversight and support of cell therapy manufacturing operations, in full compliance with established cGMP requirements.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Requirement gathering, analysis and specification; design and development, Implementation, Integration and support of web based and legacy application/systems; configuration, change and release management, build and deployment arrangement, testing and Quality Assurance including performing functional and Regression testing; developing Test Plans, Test Scenarios, Test Cases and Scripts; Will work on multiple and complex and demanding projects nationwide with frequent domestic travel required.
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In person or Remote (East Coast with initial training onsite at Bridgewater, NJ and few days for the first few months)DutiesThe CMC Regulatory Technical Writer II authors high quality Module and regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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Generate Global Quality Agreements in accordance with templates and liaise with site and Suppliers to finalize to allow Supplier Quality Director approval. + Act as a liaison between suppliers and the quality teams globally during the management of supplier quality issues.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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We are seeking an energetic and experienced Product Quality Engineer (PQE) to join our team to support the manufacturing of Cyrel®, a family of printing plates used in flexographic technology. Drive continuous improvement in quality systems and performance metrics using statistical process control (SPC) and other quality improvement tools.
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This is a leadership role which reports to both the VP, Bioethics and EVP, Chief Quality Officer. Effort is allocated as follows: 60% AI Ethics and Quality/Patient Safety 20% Academic, including AI ethics scholarship and education 20% Clinical bioethics activities.
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The Quality Engineer will work in collaboration with the development team to ensure GNY business needs are reflected in the quality and usability of the Guidewire Cloud version of Policy Center, Billing Center, and Integrations.
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Title: quality Company: Direct Line Global in Piscataway, NJ
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