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Full ownership and accountability for all Quality & Controls Assurance programs, activities and reviews, including claims reviews; call center and digital communications reviews; Medicare Risk Adjustment, HCC, clinical and coding reviews; DRG and medical records reviews; technology/systems and coding upgrade and implementation reviews (e.g. final user acceptance testing, etc.
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Our client needs a talented Data Warehouse, Quality Assurance, and Selenium Automation Tester to support Quality Assurance efforts - designing and developing test cases and executing automated and manual test methods.
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We are looking for a Senior Quantitative Developer that will be a part of a dynamic and fast-paced development team within Quantitative Research and Investment Technology supporting Fidelity Asset Management Solutions (FAMS) researchers and analysts.
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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 MassHealth Systems Teams unit seeks a highly motivated individual as a Quality Assurance Tester to join its Data Warehouse Systems Quality Assurance (SQA) team. The Quality Assurance Tester will be responsible for working on complex projects within the Healthcare Domain and applying knowledge of software testing and analysis concepts, practices, and procedures.
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Use object oriented design principles and design patterns to build high-quality solutions that allow for rapid experimentation of new models and products to reduce time-to-market. We create high quality, robust, and efficient high-responsive solutions that are used to enhance Fidelity productivity and decision-making processes.
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Must have strong knowledge of biologics and small molecules manufacturing, materials management, quality control, quality assurance and CMC regulatory requirements. The position is responsible for product development, technology transfer and overall management of CMC activities related to ensuring robust development and reliable GMP supply of oligonucleotide conjugates and intermediates.
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Work with CRO statisticians, statistical programmers and review/QC their work/deliveries; understand clinical trial design and reporting process, as well as regulatory reporting requirements including electronic data submissions and CDISC implementation; and execute and manage multiple simultaneous projects and deadlines with shifting priorities and resources in a fast-paced working environment.
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Director GMP Quality Assurance will collaborate with the CMC department and external Vendors to ensure oversight and compliance. Reporting to the Sr. Director of GMP Quality Assurance.
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Works with Chief Radiation Therapist and the Quality Assurance Specialist to develop, revise, implement and maintain policies and procedures pertinent to treatment, simulation, new programs and personnel.
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Ongoing supervision and education of Nutrition Assistant staff through review and co-signing charts for purposes of Quality Assurance required by Federal/State standards. WIC Program Nutritionist provides the full range of WIC nutrition services to applicants and participants (infants, children, prenatal and postpartum women, both breastfeeding and non-breastfeeding) under the supervision of the Senior Nutritionist.
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Quality Assurance, Associate Software Engineer in Test page is loaded. Play a major role to improve quality, functionality, reliability and usability of software products. Learn quality and coding best practices and standards, and train teams on best quality practices.
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The Quality Control Inspector will perform Required Inspection Items (RII) work in Lieu of the Chief Inspector, as well as Boroscope Inspections, Non-Destructive Testing (NDT) Inspections and other duties assigned.
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We are looking for an outstanding Quality Assurance Engineer – Requirements, Test Plans & Reports, who will convert functional requirements into test-plans for the QA Manual Testing team to execute, and summarize learning in Validation Test-reports.
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Thrives in a fast-paced, collaborative environment. ElevateBio is looking for an Associate I, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Associate I will be primarily responsible for providing Quality oversight over execution of clinical cell and gene therapy manufacturing for cGMP compliance through on the production floor interactions, review and approval of batch related documents, and events.
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quality assurance fast paced jobs Title: registered in Boston, MA
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