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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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We are currently working in a hybrid environment and are seeking to fill one full time Data Quality Analyst immediately in Boulder, CO, Boston MA. Maintain data quality through monitoring, technology-driven processes (Oracle, Snowflake, REST APIs), and statistical analysis for data completeness, correctness, and freshness.
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Experience developing quality control plans, supplier quality audits, failure analysis, and root cause corrective actions. 2 or more years of related experience in Manufacturing and/or Quality Engineering.
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As the Apheresis Quality Specialist, you'll collaborate closely with our Medical Director and enterprise Pathology Quality leadership to develop, revise, and maintain our unit's quality management plan.
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Join us at MGH and make a meaningful impact on patient care and safety through your commitment to quality and compliance in the Apheresis unit. Job Description - Apheresis Quality Specialist (3285195.
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Job Description PharmaLex is one of the largest worldwide providers of consulting services in the following focus areas: Quality Management & Compliance; Development Consulting & Scientific Affairs; Regulatory Affairs; and Pharmacovigilance, Epidemiology and Risk Management.
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Assists in the development and maintenance of a detailed schedule of QA/Reg milestones and deliverables; to include internal audits, quality improvement projects, Trial Master File (TMF) reconciliations, etc.
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The role works closely and have high visibility with Executives, VP's and Directors of Engineering, Infrastructure, SRE, Product Management and Customer Support to ensure overall software quality in development pipeline all the way to production regions, and to set the strategy for developing high-quality software to solve complex problems for our customers and users.
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The Quality Assurance (QA) Associate is responsible for utilizing lab equipment to test finished products and product components to ensure all are within specified parameters. Identifies and reports quality results and trends to Lab Supervisor, the Lab Manager and the Quality Improvement Specialist.
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Three years experience in Quality Control and practical knowledge of commercial heat treatment of steel, aluminum, titanium, nickel, brass, copper, etc. Assist in general quality activities including control of quality records, monitoring quality objectives at all levels, implementing, monitoring, and maintaining the BMS, evaluation/disposition of non-conformances, audits (on-site and internal), implementation, and support of the navigator operating system.
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The Associate Director, Biomarker Operational Quality will provide biomarker quality leadership and oversight across GxPs-related to research and development, implementation into clinical trials and potential commercialization of clinical biomarkers into IVDs. This leader will collaborate with business partners and GCP Operational Quality to drive quality outcomes and operational excellence.
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S/he would also provides support for the NACA’s Mortgage Operations in providing quality control and auditing for the various NACA departments. The QA Analyst is responsible for the overall evaluation of NACA systems and software to ensure they are free of defects and meet the quality standards of the organization.
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Minimum of 6 years of experience in drug safety/pharmacovigilance quality assurance or compliance within the pharmaceutical or biotech industry. Certification in pharmacovigilance (e.g., RQAP-GLP, PVQA) or quality management (e.g., ASQ Certified Quality Auditor) is a plus.
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The Department of Quality and Patient Safety (QPS) supports Dana-Farber Cancer Institute’s mission to reduce the burden of cancer at Dana-Farber and beyond by educating, inspiring, measuring, improving, and innovating to advance quality across the cancer care continuum.
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We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of manufacturing, testing and release activities for SMPA, its partners, contract testing laboratories, and suppliers of drug substances and drug products used for investigational clinical trials and/or commercial phases.
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Title: quality Company: Waukegan Hospital in Jamaica Plain, MA
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