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Internal Audit Senior Manager- Quality Assurance & Reporting. Other essential duties and responsibilities in quality assurance include: troubleshooting quality issues; ensuring compliance with laws and regulations; documenting and rolling out quality guidance; and training and mentoring team members to maintain enhanced quality standards.
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We seek a Sr. Director, Quality Assurance in CMC team to support the Acoramidis (AG10) program and all BridgeBio Cardiorenal programs. At least 15 years of progressively responsible experience in Quality Assurance within the pharmaceutical industry; 5 years prior management or leadership role preferred.
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Reporting to the Executive Director, Clinical Quality Assurance, the Associate Director/Director, Clinical Quality Assurance will define and support the quality oversight and management of GCP activities internally at BBGT (and other affiliates as directed) and externally with BBGT vendors, consultants, and service providers, including, but not limited to, quality systems management, document review, and approval.
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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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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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Title: Manager/Senior Manager, Quality AssuranceReports To: Associate Director, Quality Assurance Operations Location: Redwood City, California Classification: Exempt Overview:The Manager/Senior Manager, Quality Assurance, represents the quality organization at Coherus and at Contract Manufacturing Organizations (CMOs) to ensure appropriate oversight/monitoring of production, and ensure continuous supply of clinical and commercial products.
$110,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work closely with manufacturing, CMC and science teams on quality assurance tasks. Desired QualificationsProven experience (5+ years) in quality assurance, ideally within clinical-stage manufacturing for a biotech company.
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This position provides hands-on technical guidance and leadership from a Quality perspective to the team throughout all stages of product development up to and including technology transfer and commercialization.
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Demonstrates working knowledge of quality assurance systems, methods and procedures. An accountable team player who is detail and quality oriented with solid understanding of quality assurance principles, systems, and procedures.
$99,790 - $129,140Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Track and monitor quality assurance metrics. As a QA engineer you will help us design and develop test automation to ensure product quality and improve users’ experience. 4+ years of quality engineer experience with a solid background in writing automated tests.
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Communicate and document design decisions and collaborate closely with other team members in business and development, partnering to resolve implementation issues and ensure quality. Strong knowledge of cloud computing resources (e.g. AWS, Google Cloud, Azure.
$59.14 - $78.37 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Partner on continuous development and enhancement audit methodology and frameworks related to internal and external quality assurance programs, establish consistent standards for audit execution while ensuring compliance with IIA requirements.
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Northrop Grumman Marine Systems is seeking a Quality & Mission Assurance Manager 2 to lead Quality Engineering, and Mission Assurance activities in support of the Marine Systems Business Unit operations in Sunnyvale, CA. The manager should be knowledgeable in aerospace and/or military quality and mission excellence processes and requirements.
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Skills: Biotechnology, GMP, GLP, Cellular products, Batch records, Quality Control, Quality Assurance. Have you had a minimum of 5 years Quality Assurance experience in pharmaceutical or biologics.
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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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Title: quality assurance in Palo Alto, CA
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