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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 Quality Assurance Engineer, reports to the Quality Assurance Manager and is responsible for implementing the Quality program for Caltrain for individual capital Projects and for the maintenance program of the Peninsula Corridor Joint Powers Board (Caltrain.
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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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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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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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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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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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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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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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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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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.
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This new, security-first division was created to bring heightened focus and governance to our data protection policies and content assurance protocols to keep. Job Overview:As an Access Assurance Analyst, you will be part of the team responsible for Access Assurance within TikTok USDS. You will be responsible for supporting the team along with a team of cross-functional cyber, privacy, engineering, and data protection analysts to define, implement, manage, and measure controls to protect data in accordance with USDS policies and standards relevant to geographical regulations, contractual commitments, and confidentiality requirements.
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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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As a Quality Assurance Engineer, you will work under the guidance of the Quality Assurance Project Managers and Quality Assurance Deputy Director, to apply standard quality assurance.
$108,000 - $163,000 a yearFull-timeExpandApply NowActive JobUpdated 24 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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Title: assurance Company: Epm Scientific in Stanford, CA
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