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The Director of Clinical Quality Assurance (CQA) is a hands-on position responsible for all assigned activities that ensure Pliant Therapeutics sponsored clinical trials adhered to applicable GCP regulations (e.g., FDA, ex-US, country-specific), ICH guidelines, Pliant Standard Operating Procedures (SOPs), and current industry standards and practices.
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What does a successful Commerce Hub Quality Assurance Engineering Director do at Fiserv? Commerce Hub Quality Assurance Engineering Director opportunity is to ensure, that the delivery is of the best quality, predictable and consistent.
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Kyverna is recruiting a highly motivated Associate Director, Patient Operations – Quality Assurance in its Technical Operations organization to help advance its mission to free patients from the siege of autoimmune disease.
$165,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Provide compliance advice and guidance to achieve continuous quality improvement and effective quality assurance. At least 10 years of experience in Clinical Quality Assurance.
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Regional Director, Product Integrity & Quality Assurance -Latin America. Expertise in running AQL, Lean, Six Sigma quality management. Experience driving global quality programs for premium consumer products across Apparel and Home businesses.
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Prior role as Compliance Officer, Quality Assurance Director or equivalent for a nonprofit, government or health care organization and/or extensive experience in compliance, risk management, or a related field in a senior leadership role.
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Assist in the enhancement of Quality Assurance and control policy, and risk identification and mitigation by providing consultation & recommendations to regional and Global QA Management.
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Knowledge of GLP and GCP, Pharmacovigilance (PV), ICH, FDA requirements and guidelines for small molecules, including drafting, interpreting, and implementing quality assurance policies and procedures for regulatory documents, as well as establishing document management activities.
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10 years experience Quality Assurance experience in pharmaceutical, technical, or related area including GXP Quality Assurance experience. Provide Quality Assurance support, guidance and management of Quality Issues, as assigned.
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Senior Director of GCP Clinical Quality Assurance. GCP Clinical Quality Assurance, Senior Director. 8 years GCP Quality Assurance experience. Prior experience/in-depth knowledge of clinical quality assurance.
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The Director of Clinical Quality Assurance (CQA) will be responsible for Quality Assurance oversight of multiple 4DMT sponsored clinical trials, ensuring trials are executed in compliance with all applicable international regulatory requirements for Good Clinical Practice (GCP.
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Supports the Zymeworks Clinical Quality Assurance (CQA) team to ensure development and implementation of Clinical Quality strategy, processes, procedures and standards as required by applicable regulations.
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They are looking to add a leader to their Quality Assurance team in one of their phase III trials. Act as the primary contact for vendors, contract facilities and contract service providers related to quality aspects of clinical trials.
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The Associate Director of Clinical Quality Assurance will be responsible for building the clinical quality assurance processes and providing quality oversight for the clinical programs and CRO throughout the development stages of antibody-based radiopharmaceuticals.
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