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Requirements: BS degree in Chemistry, Biochemistry, Molecular Biology, Virology or related scientific disciplines or equivalent experience, + 15 years of experience, 5 years of experience must be in Quality Control or cGMP laboratories.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Demonstrated an ability to manage and influence Quality Control testing at contract laboratory facilities and ensure alignment with Gilead's GMP policies. Sr. Research Associate II, Biologics Quality Control.
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Adverum's core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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Basic knowledge of QMS (Quality Management System) and Core Quality tools such as Process Flow Chart, PFMEA (Process Failure Mode Effect Analysis), Control Plan, and Measurement System Analysis.
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What are the ongoing responsibilities of a Senior Valuation Analyst? What is the Senior Valuation Analyst responsible for? Demonstrated ability to utilize quantitative, statistical, and mathematical financial techniques for independent fair valuations of securities including prior experience in model development, risk, valuation, and model validation development and implementation for Structured Products, Foreign Exchange, Equity, Fixed Income and OTC derivatives.
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Job Summary:The Global Security Operations Center Analyst, assigned to one of Pinkerton's largest global clients, conducts in-depth research, open-source analysis, and social media review to monitor threats that may impact the safety and wellbeing of the client's executives, operations, and/or assets.
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Process Flow Diagrams, Process FMEAs, Process Control Plans, SPC, MSA, Process Capability) Fully literate in Microsoft computer applications such as Word, Excel, and PowerPoint Preferred Qualifications: 4+ years of experience in quality, supplier quality, or manufacturing in one of the following industries: Automotive, aviation, computer, or medical device Experience creating and improving quality systems Working knowledge of quality systems.
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Manage control of external suppliers and contract manufacturers to ensure the supply of quality materials. Collaborate with suppliers on the creation and maintenance of quality tools such as FMEAs, control plans.
$183,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Hands-on experience in software quality assurance and ability to emphasize and influence the stakeholders to apply software testing standards in SDLC. Support development and implementation of the technology and process roadmap for the IT Quality Engineering domain.
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You produce high-quality work with a comprehensive understanding to confidently address questions from stakeholders. Prior experience with financial planning tools (Planful, Anaplan, Adaptive Insights, etc.
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We are seeking a highly skilled Information Security Governance Third-Party Risk Analyst who will assess third-party risk as part of vendor evaluations. Job Title: ISG Third-Party Risk Analyst.
$80 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The People Analytics/HR Data Analyst is responsible for leading the people analytics functions at the client. The People Analytics/HR Data Analyst is responsible for leading the people analytics functions at the client.
$90 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Requirements:You have:Experience with Biologics Quality Control sub-functions and extensive knowledge of industry best practices and trends. Must be able to develop and improve complex concepts, techniques, and standards and new applications based on quality principles and theories.
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Serve as the site’s Quality Business Process Owner for QMS processes (e.g. Quality Risk Management, Data Integrity, Change Control. 4-6 years of experience in Quality Assurance/Systems, or related role within the biotech/pharmaceutical and/or cell/gene therapy industries.
$187,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Qualifications: Bachelor of Science degree or work experience equivalent to a minimum of 5-7 years of experience in a GMP quality (Mfg/QA/QC) environment, experience in drug substance. Review and approval of cGMP documentation, such as master batch records, executed production records, certificates of analysis, and any other quality related records, to support the disposition of Coherus products.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated Today
Title: quality control analyst Company: Ryco Biosolutions in Burlingame, CA
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