• MRI Tech Alzheimer's Imaging Department Part Time

    Banner Health (Phoenix, AZ)
    …disease therapies. Our work supports early-phase clinical trials as well as FDA -approved treatments such as lecanemab and donanemab. This is a truly exciting ... meaningfully to the fight against Alzheimer's disease by delivering the high- quality imaging data researchers need to develop life-changing therapies-and ultimately,… more
    Banner Health (12/24/25)
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  • Validation Engineer IV

    PCI Pharma Services (Bedford, NH)
    …as well as cross-functionally with Manufacturing, Engineering, Critical Utilities, Quality Assurance, and project management to achieve all project deliverables. ... Skills:** + Knowledge of Industry guidelines (ISPE, PDA), US and international regulations ( FDA , ICH, ISO, EMA) for validation of GMP facilities. + Possess strong… more
    PCI Pharma Services (12/24/25)
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  • Staff Software Build Engineer (Hybrid)

    Stryker (Redmond, WA)
    …engineers and cross-functional teams to ensure the timely delivery of high- quality software builds, complete with robust documentation and streamlined deployment ... your career. ​ **What You Will Do** + Collaborate with Engineering, Operations, Quality Assurance, and Project Management teams to define and execute software build,… more
    Stryker (12/24/25)
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  • Technical Trainer I - In-Life

    Charles River Laboratories (Ashland, OH)
    …systems. + Review documentation of functions performed as part of quality control requirements. + Use, maintain, and troubleshoot instrumentation and equipment. ... None + Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and… more
    Charles River Laboratories (12/24/25)
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  • Director, IT Applications

    Sumitomo Pharma (Boise, ID)
    …warehouse environment. + Ensure that all SAP solutions adhere to **GXP, FDA , and other regulatory requirements** applicable to the pharmaceutical industry, ... and enhancement initiatives, ensuring alignment with budget, timeline, and quality standards. **Implementation & Optimization** + **Direct and govern end-to-end… more
    Sumitomo Pharma (12/23/25)
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  • Associate Director - Tech@Lilly MQ, Engineering…

    Lilly (Indianapolis, IN)
    …geographically dispersed group of business and technical colleagues + Strong knowledge of GxP, FDA , and other regulatory requirements. + Ability to work in a ... : You will be part of Tech at Lilly MQ (Manufacturing and Quality ), an organization that drives manufacturing operational excellence and productivity efforts through… more
    Lilly (12/23/25)
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  • Physician - Clinical Pathology Section Chief

    Veterans Affairs, Veterans Health Administration (Aurora, CO)
    …Pathology (CAP), the Joint Commission (TJC), the Food and Drug Administration ( FDA ), VACO, and the American Association of Blood Banks (AABB). Ensures accurate ... the clinical laboratory is monitored continuously and results recorded in the Quality Assurance (QA) minutes. The Section Chief, Chemistry and Toxicology selects the… more
    Veterans Affairs, Veterans Health Administration (12/21/25)
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  • Principal Engineer, Body Control Subsystem…

    General Motors (Warren, MI)
    …should be an experienced leader who cares deeply about software and software quality . As a Principal Software Engineer, you will be responsible for broad oversight ... and ownership of safety and regulatory design compliance for all features in the Body...and engineering teams through effective executive communication + Maintain high- quality bar in projects from the start and champion… more
    General Motors (12/19/25)
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  • Contract Administrator, MI

    Fujifilm (Bismarck, ND)
    …are followed and consistent across all zones. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all ... follow-up, and administration with a focus to provide high quality and efficient support to all MI teams, including...with all applicable S. Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO… more
    Fujifilm (12/17/25)
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  • Research Services Clinical Science Professional…

    University of Colorado (Aurora, CO)
    …from research in an accurate and timely manner + Evaluate data sets for quality and completeness. Set up and or run statistical analyses. + Analyze data, including ... statistical analyses and qualitative assessments of data and data quality . Identify and help solve gaps in data collection....solve gaps in data collection. + Adhere to research regulatory standards + Maintain detailed records of studies to… more
    University of Colorado (12/17/25)
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