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The Quality Assurance Analyst (“QA Analyst”) will be primarily responsible for systematically testing both new and existing functionality, identifying issues, troubleshooting, and putting forth recommended solutions.
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The Senior Director, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as vendors supporting Scholar Rock sponsored Clinical Studies.
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Executes quality assurance reviews of core audit activities i.e. audits, issues validation, audit plan documentation and coverage, and other special projects, using predefined attributes and challenge questions, relevant for the review type and in accordance with the QA strategy.
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As the Quality Assurance Testing Lead, you will play a central role in the SAP Employee Central implementation project, contributing to the seamless operation of our HR systems. Proven experience as a Quality Assurance Testing Lead in SAP Employee Central or similar HR software implementations.
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Assist the BEST Program QA and Test Lead in all aspects of the Software Development Life Cycle (SDLC) methodologies, including executing quality assurance best practices and implementing quality controls.
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Trillium Professional is now seeking a Quality Assurance Test Manager in Boston! The BEST QA Test Manager plays a critical role in ensuring the quality and compliance of the software solution with Commonwealth functional and technical requirements.
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GMP quality assurance experience in the pharmaceutical or biotechnology industry. The Sr Specialist Quality Assurance will be responsible for quality review of production and testing of clinical trial materials at external manufacturing site.
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Experience in apheresis, cell therapy/stem cell transplantation, bone marrow transplant, hem/onc, laboratory medicine, and/or regulatory compliance/quality assurance preferred. Join our team at Massachusetts General Hospital (MGH) as an Apheresis Quality Specialist and play a crucial role in maintaining the integrity of our Apheresis unit.
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Oversee quality assurance activities to ensure the integrity, accuracy, and compliance of clinical trial data within Veeva Vault applications, in accordance with regulatory requirements (e.g., FDA guidelines, GCP standards.
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Years’ experience: 5 or more years of relevant test and quality assurance experience with 3 years’ experience in system and subsystem testing. Manage testing efforts required to deliver the highest quality to the customer.
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The Associate Director, Lab Operations Quality Assurance, will work as part of a new product team, focused on improving blood-based cancer diagnostic capabilities in areas such as cancer detection, minimum residual disease, and other related applications.
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Bachelor’s degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 8 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
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Undertake model audits, quality assurance reviews, and support best practices complianceCoordinate appraisal review and commentary by regional Asset Managers and conduct variance analysis to external appraisalsSupport Asset Manager in oversite of leasing, property management, and capital projects.
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Minimum of 15 years professional working experience in Pharmaceutical Industry, including Manufacturing, Quality Control, Quality Assurance, CMC, Regulatory or related compliance experience with at least 5 years aggregate experience performing audits for GMP, ISO or ICH, and hosting/supporting FDA, EMA, MHRA, AIFA, ANVISA and/or other regulatory inspections.
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We provide Next Gen QA offerings like System Modernization assurance, Business Process Assurance, Quality Engineering, Cloud Platform Assurance, Customer Experience Assurance and Robotic Test Automation.
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assurance job Title: quality assurance tech Company: Kforce Inc in Boston, MA
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