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The Director is responsible for development, implementation and oversight of the Quality Assurance (QA) and Performance Testing (PT) programs to ensure compliance with Department of Energy (DOE), National Nuclear Security Administration (NNSA), Los Alamos National Laboratory (LANL) and Northern New Mexico Integrated Security (N2MIS) directives and contract requirements.
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Northrop Grumman is in need of a Director 1 - Mission Assurance and can be based at its Elkton, Maryland or Rocket Center, West Virginia facilities. The Director 1 Mission Assurance (MA) is responsible for overall leadership of Northrop Grumman's Missile Products Business (MP) Unit's Quality & Mission Assurance organization, including Mission Assurance, Program / Product Quality, Supplier Quality, Quality Management System Compliance, Metrology/Calibration, Software Quality, Non-Destructive Inspection, Audits and Training.
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The IFF Director of Quality Assurance is responsible for ensuring and supporting operational quality and compliance across all International Freight Forwarding sites. Develop relationships with Senior Leadership, Product Owners, Branch Managers and Corporate Business Partners- especially the YLA Corporate Quality & Regulatory team to improve and maintain quality assurance within IFF.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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This position reports directly to the Enterprise Risk Management (ERM) shared services director responsible for independent control testing, ERM analytics, Archer GRC, and the ERM Continuous Improvement Office and will work closely with the Liquidity Risk Oversight team to build, execute, and oversee the Conformance Testing Program.
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The Regulatory Reporting Conformance Testing Program provides assurance over the completeness and accuracy of Huntington’s interpretation of regulatory reporting instructions and implementation using bank systems and business data.
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Relevant certifications such as Certified Public Accountant (CPA), Certified Information Systems Auditor (CISA), Certified Internal Auditor (CIA), etc. This leadership role requires a strong blend of technical and soft skills, including but not limited to regulatory reporting, liquidity, data management, technology, risk management, negotiation, critical thinking, team building, relationship building, creative problem solving, and more.
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Proficiency with SQL, Python, SAS, R, or related languages for reporting and data analysis. Prior experience with regulatory reporting, auditing, risk management, and/or data management at a large financial institution strongly preferred.
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Maintain up-to-date knowledge of financial and regulatory reporting requirements to provide constructive feedback and recommendations intended to enhance risk management practices and the accuracy of the regulatory reporting process.
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Quality Assurance Director, Clinical. 15+ years of experience in clinical quality assurance (GCP, GLP, and PV) in cell and gene therapy/biotechnology or the pharmaceutical industry.
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Reporting to the Vice President of Quality Assurance, the Senior Director of QA Compliance will provide leadership, direction and oversight of Quality compliance activities. 12+ years of experience in quality assurance supporting GxP operations.
$285,608 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Quality assurance, Good Clinical Practice, ICH-GCP, ICH-PV, FDA, SOPs, QMS, biotechnology, pharmaceutical, biologics. You will be responsible for leading the development, implementation, and maintenance of quality assurance (QA) systems and activities to support quality oversight in Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Pharmacovigilance (PV) operations.
$100 an hourExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams; Partner with the teams to ensure appropriate and timely documentation of quality event management, including CAPA plans supporting product pipeline.
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Under the supervision of the Executive Director, the Clinical Quality Assurance Director will be responsible for the oversight of internal and external contract auditing and documentation.
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Director of Quality Assurance reports to the CEO. This position is the day to day leader of the Quality function and provides guidance and leadership from Quality and Regulatory perspective to the team throughout all stages of product development.
$235,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are hiring a Director of Quality Assurance to work onsite in El Segundo. The Quality Director must ensure that functional managers and employees across the company are in compliance with the rules and regulations of regulatory agencies and applicable industry standards; and that the company Quality Management System (QMS) Policies, Procedures, and Work Instructions are being followed, and behavior in the organization meets the company's Standards of Conduct.
$199,980 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago
Title: director assurance Company: Fergene
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