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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 - $129,140 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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 Director of Clinical Quality Assurance (CQA) is a hands-on position responsible to 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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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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Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. Interact with key stakeholders such as Formulation and Process Development, Manufacturing, Engineering, Packaging, and Regulatory Affairs to ensure that Clinical/Commercial material is manufactured in accordance with established procedures, cGMPs, and appropriate regulations.
$99,790 - $129,140 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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The Staff Quality Assurance role for Beckman Coulter Diagnostics supports cross-functional core team members in the software product design and development lifecycle of the Microbiology Business Unit in West Sacramento, California.
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Minimum 12 years of GCP/GVP Quality Assurance experience. Alumis is hiring a Clinical Quality Assurance Sr. Director, reporting to the VP of Quality. This position requires expertise in Good Clinical and Pharmacovigilance Practices (GCP & GVP) and relevant US and EU regulations.
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Audit & Assurance Senior (Anywhere in US) Overview: We are a forward-thinking, full-service accounting firm providing modern solutions to businesses across the globe. We focus on comprehensive assurance, tax, and consulting services for our clients, and we provide our people and our community with the resources to lead meaningful and purposeful lives.
$150ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The ideal candidate will have extensive experience leading GMP quality assurance activities and deep understanding and demonstrated working knowledge of CFRs, ICH guidance documents, and other regulations that govern GMP compliance during clinical development and commercialization of small molecule drug product.
$252,000 - $308,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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We are seeking a dynamic and seasoned Quality Professional who can bring strategic expertise and strong leadership skills, while also maintaining a hands-on approach to further build the Quality function at HI-Bio. The VP, Quality Assurance will have end-to-end Quality responsibilities inclusive of leading GMP, GCP, and GLP functions.
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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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Interact with key stakeholders such as Formulation and Process Development, Manufacturing, Engineering, Packaging, and Regulatory Affairs to ensure that Commercial / Clinical Drug Products are manufactured in accordance with established procedures, cGMPs, and to appropriate regulations.
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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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Ensuring Compliance: The QA Manager ensures that all testing and quality assurance processes comply with industry standards and regulations. The ideal candidate is a quality assurance leadership expert with strong communication skills and previous experience as a detail-oriented QA engineer.
$158,000 - $219,000 a yearFull-timeExpandApply NowActive JobUpdated Today
Title: assurance Company: Epm Scientific in San Mateo, CA
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