• Utilities and Facilities Technician

    Fortive Corporation (Irvine, CA)
    …maintenance, building utilities, or related technician role in a GMP, FDA -regulated, or cleanroom environment. + Experience maintaining and troubleshooting critical ... startup spirit. Our forward-looking companies lead the way in software -powered workflow solutions, data-driven intelligence, AI-powered automation, and other… more
    Fortive Corporation (08/19/25)
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  • Quality/Validation Engineer

    TEKsystems (San Diego, CA)
    …Flexibility to occasionally work 2nd shift. + Proficiency in statistical analysis software (eg, JMP, Minitab). + Familiarity with project management tools (eg, JIRA, ... such as medical devices, aerospace, or automotive. + Experience with ISO, FDA , or other compliance frameworks. + Proven success leading cross-functional validation… more
    TEKsystems (08/16/25)
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  • Coordinator of Patient Administration - San Diego

    ZOLL Medical Corporation (San Jose, CA)
    …that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients ... (https://www.zoll.com/products/supersaturated-oxygen-therapy/therox-sso2-system) Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to… more
    ZOLL Medical Corporation (08/16/25)
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  • Neuroscience Account Manager - Psychiatry - East…

    Lundbeck (Oakland, CA)
    …including accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products. ... customer influence network + Must be computer literate with proficiency in Microsoft Office software + Must live within 40 miles of territory boundaries + Driving is… more
    Lundbeck (08/15/25)
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  • Director, Quality Assurance, Digital Solutions

    Abbott (Sylmar, CA)
    …for a diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices, and digital health platforms. ... strategy for Digital Solutions + Ensure compliance with all applicable standards and regulations (eg, FDA 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, EU MDR) +… more
    Abbott (08/15/25)
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  • Executive Director of R&D Global Quality (Remote)

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …**Qualifications** + Bachelor's degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of ... be considered for employment. We will also not offer you money to buy equipment, software , or for any other purpose during the job application process. If you are… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Production Lead

    PRIDE Industries (Auburn, CA)
    …104, Part 5 - Sherman Food, Drug and Cosmetic Law: 2008, and FDA 's Quality System Regulations, preferred; * Knowledge of planning, forecasting, and scheduling in ... including knowledge of word processing, spreadsheet, database and presentation software ; * Basic mathematical ability including addition, subtraction, multiplication,… more
    PRIDE Industries (08/14/25)
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  • Reliability Engineer (Regulated Industry)

    Mentor Technical Group (South San Francisco, CA)
    …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... and problem-solving skills. + Proficiency in CMMS and asset management software , preferably SAP. + Excellent communication and collaboration skills. + Ability… more
    Mentor Technical Group (08/14/25)
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  • Project Manager

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …be responsible for managing Sustaining Engineering projects in accordance with FDA regulations and company standards. The Project Manager's primary duties include ... Sigma, Scrum) and processes + Proven experience using project management tools and software (ie Microsoft Project, Office 365, One Plan etc) + Strong interpersonal… more
    BD (Becton, Dickinson and Company) (08/14/25)
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  • Clinical Research Coordinator I (Part-Time)…

    Cedars-Sinai (Santa Monica, CA)
    …to Sponsor, FDA , and IRB requirements. + Ability to use software applications (MS Office Suite - Excel, Word, Outlook, PowerPoint) and operate technological ... devices (eg, computer, laptop, tablet, smartphone, etc.). + Establishes effective working relationships with cross-functional team(s). + Collaborates to solve problems and make decisions to achieve desired outcomes. + Cultivates and maintains strong customer… more
    Cedars-Sinai (08/14/25)
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