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We are seeking a qualified individual to join us as the Manager of Quality Assurance at our Menlo Park facility. In 2019, we expanded into Milpitas, CA for non-clinical production and in 2022, completed our cGMP patient specific cancer vaccine peptide production facility.
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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 control's ecosystem.
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This position reports to the Quality Assurance Manager and QA Director. The Behavioral Health Quality Assurance Manager (QA Manager) is responsible for overseeing and implementing quality assurance processes within the behavioral health clinic.
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Experience in a quality assurance role, bringing an in-vitro diagnostic product (or products) through the FDA process. 8+ years of Quality Management, Quality Assurance, and Quality Control leadership experience in Diagnostics, Biotechnology, or relatable life sciences fields.
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We are looking for an expert Quality Assurance Professional with experience advising research and development teams in Good Clinical Laboratory Practices (GCLP) quality strategy within a pharmaceutical organization.
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The Associate Director/Director of Quality Assurance, reporting to VP of Quality & Regulatory, will be responsible for Quality Assurance and Validation team to ensure that the Quality management system and all aspects of cGMP are effectively established, implemented, and maintained in accordance with the regulations for manufacturing of guide RNAs for gene therapy applications.
$150,000 - $200,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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EPRI is looking for a Software Quality Assurance (SQA) Student Engineer to assist with testing software for usability and writing reports documenting errors. Software Quality Assurance Student Engineer.
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Direct Quality Assurance projects through the Leadership Team to sustain regulatory compliance and support company goals/continuous improvement efforts. Comply with all quality policies, procedures, and practices through consistent application of sound quality assurance principles.
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The Manager of Clinical Quality Assurance (CQA) is a key member of the CQA team and will perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept.
$144,800 - $170,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance, who will play a key role within Quality Assurance and is responsible for providing leadership and compliance support for RevMed sponsored clinical trials with respect to RevMed's Standard Operating Procedures, applicable regulatory requirements (FDA, EU, ICH & country-specific), and current industry standards and practices.
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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.
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We are seeking a Quality Assurance Manager who is hands-on engineering leader to build out a new team focused enhancing automation coverage and effectiveness across the Family of Apps. You will have a great influence on the whole quality assurance process and methodology for the product development.
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Serves as advisor and spokesperson to management and represents Quality Assurance function on major matters pertaining to its policies, plans, and objectives. The Quality Assurance Unit (QAU) Manager leads the SRI Biosciences Division’s Quality efforts.
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This role will support the quality assurance, clinical surveillance, and post- positive provider outreach programs. Assisting in the clinical review of data for use in Quality Assurance/Quality Improvement (QA/QI.
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Provide resolution of quality assurance issues/documentation in compliance with LCGM policies, cGMP, and Institutional Review Board (IRB) protocols. We seek an energetic Clinical Manufacturing Quality Assurance Analyst, who shares this vision, to support the development, implementation and maintenance of our quality assurance program.
$34.62 - $41.83 an hourFull-timeExpandApply NowActive JobUpdated 12 days ago
Title: assurance Company: Epm Scientific in San Carlos, CA
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