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Operating from the Eastern Shore of Maryland in the idyllic town of Easton, Fusion ESG is a Technology Integration Contractor (TIC) that provides turnkey design, engineering, implementation, logistical, project management, and quality assurance solutions and services to mission-critical facilities worldwide.
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HRV Conformance Verification Associates, Inc. supplies a highly integrated series of professional engineering and quality assurance/quality control services worldwide that span the steel, concrete, paint, mechanical, and construction industries.
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The Good Clinical Practice (GCP) Senior Quality Assurance (QA) Auditor is crucial in ensuring that clinical trials are conducted ethically, with integrity, and in compliance with regulatory requirements and GCP guidelines.
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The Wealth Management Advisor partners with affluent clients to identify their financial goals, analyze their financial landscape and develop recommendations that help them work towards well defined financial objectives.
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SUMMARY The purpose of the position is to provide a Quality Assurance (QA) Engineering Technologist to support projects within SAO that have the complex, contractually mandated quality assurance requirements associated with NASA space-flight hardware fabrication and to provide guidance to CFA scientific investigators in defining, proposing, and conducting instrumentation projects with quality assurance requirements.
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Any specific experience with data management best practices, data governance, data quality controls, regional or regulatory reporting requirements is preferable. The person will work directly with stakeholders across – ESG Investments, ESG Product Strategy, ESG Data and Operations, Client, Product and Regulatory Reporting, and Enterprise Risk Management to understand their data and reporting requirements and to translate requirements into functional specifications for technology partners building/ enhancing IT solutions for ESG reporting.
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Rehab Systems Management Provides supervision in all areas of the Day Hab Systems reporting standards to ensure organizational compliance with all DMA, DDS regulations. Must have experience with Day Hap (MA Health) system and DDS (HICSIS)Quality AssuranceProvide input in programs and preparation for CARF, DDS survey and annual DMA audits.
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The Change management consultant interfaces with stakeholders in the GREFP and TBS organizations, and other supporting departments and within the program scope. Degree in Psychology, Sociology, Organizational behavior, Business Management, or other degree with relevant Organizational Change Management (OCM) experience Is knowledgeable and experienced in (end) user journey best practices Knows his/her way in innovative ways to create awareness and build proficiency.
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Under the oversight of the Director, Research Compliance/Assurance & Programs administers the institution’s Human Research Protection Program (HRPP) including the Institutional Review Board/Committee on Human Studies (IRB/CHS.
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Master Data Management / Data Quality Management / Governance Collibra, Atacama, Alation, Reltio etc. Data bases (SQL, NoSQL) and Data Platforms (Databricks, Snowflake) Strong skills with Database management, Data modeling and design DevOps and Security CI/CD, Serverless compute, OAuth, SSO, MFA etc.
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As part of the GMP Operational Quality group primarily responsible with providing quality oversight and support to Vertex Cell and Gene Therapy operations in the following key areas/activities; support of manufacturing operations across all phases of development and commercial, support of analytical laboratory, materials management, and facility/engineering groups.
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The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) are effective and compliant with applicable requirements, provide leadership and guidance re: CLIA and associated regulations, and support the Lab Director and leadership in maintaining audit readiness.
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Experienced in use of Quality Management Systems such as Veeva, Trackwise Digital, Valgenesis, SAP. Minimum of 10 years' broad experience in the pharmaceutical industry; preferably in Oral Solid Dose with strong background in associated Analytical testing, manufacturing and Quality Assurance in support of pharmaceutical development operations.
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The Software Quality Assurance Testing Engineer will play a key role in the quality assurance of Anti-Money Laundering ("AML"), Sanctions Screening, AML Transaction Monitoring, and Know Your Customer ("KYC") suite of applications in the Boston, MA area.
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Experience in electronic Enterprise Management systems, Quality Management Systems, Document Management Systems. ElevateBio is looking for a Cell Therapy Manager, QA Operations to join their growing Quality Group at our BaseCamp facility in Waltham, MA. In this role, the Manager 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 supplier management jobs Title: director in Cambridge, MA
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