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About The Team: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.
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Adverum is looking for an Executive Director (ED) of Quality Assurance to join our team in our Redwood City office. Experience developing and managing late-stage clinical and commercial Quality Assurance organizations.
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Familiarity with and interest in HV battery systems, hardware testing, quality assurance, metrology, exposure to mass production environments. Experience in STARCCM+, COMSOL, MATLAB, Simulink, Ansys.
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We are seeking a skilled GMP Quality Assurance Manager to join our client. Proven experience in a GMP quality assurance role within the biotech or pharmaceutical industry. The ideal candidate will bring extensive experience in quality assurance within the biotech field, specifically with commercial quality complaints, solid oral dosage forms, and batch record review.
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The Senior Director works internally with other members of Global Supply Chain (GSC) and other Gilead functions - e.g., Clinical Development, Clinical Operations, Product Development & Manufacturing (PDM), Quality Assurance, Regulatory, and Project Management Office - to develop and formulate supply chain strategies, meet project deliverables, solve business problems and create competitive advantage.
$307,560 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Strong clinical supply management experience/knowledge in forecasting, demand/supply planning, IRT systems, inventory management, clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and GXP regulations.
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The Petroleum Product Tanker Driver's responsibilities include safe product handling, product quality assurance, and product transportation consistent with regulatory compliance and Company operating goals.
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Experience in a quality assurance role, bringing an In-Vitro Diagnostic (IVD) product (or products) through the FDA process. Manage all aspects of the quality assurance lifecycle including scheduling, planning, issuing agendas, executing, issuing reports, evaluating responses, requesting clarification, corrective and preventive actions (CAPA), and closing.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Work in close cross-functional collaboration with Clinical Operations, Regulatory Affairs, Program Management, Quality Assurance, Biometrics and Data Management, Pharmacovigilance and Clinical Research Organizations (CROs.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Proven track record of successfully leading quality assurance teams and driving continuous improvement initiatives in a pharmaceutical manufacturing environment. Collaborate with cross-functional teams, including Research & Development (e.g. clinical development, clinical operations), manufacturing, supply chain, and regulatory affairs, to ensure alignment and integration of quality assurance processes throughout the product lifecycle.
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Revolution Medicines is seeking a Senior Manager, GMP Quality, who will play a key role within Quality Assurance and is responsible for providing leadership and operational support for RevMed programs through different phases of development.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Performs a variety of basic and complex Laboratory procedures, including phlebotomy, specimen processing, quality control, quality assurance, and waived, moderate or high complexity testing (as classified by the Clinical Laboratory Improvement Amendments - CLIA.
$83.13 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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We are looking for passionate Clinical Laboratory Associates (CLA) to be responsible for assisting our day-to-day operations, providing equipment maintenance in the clinical laboratory, completing the pre-analytical phase of testing (e.g., specimen receipt, accessioning, and plasma/buffy coat isolation), performing quality assurance procedures, while complying with all local, state, and federal laboratory requirements.
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The Internal Audit function provides independent, objective, reliable, valued and timely assurance regarding the effectiveness of governance, risk management, and internal controls that mitigate current and emerging risks and help strengthen the internal controls' ecosystem.
InternExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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The candidate will be reporting to VP of Quality Assurance and is responsible for the strategic development and management of QA operations to support CMC operations and clinical activities in compliance with FDA, ICH, EMA regulations, guidances, industry standards, and company policies.
$260,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
assurance job Company: Google in Foster City, CA
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