• Associate SAP Enterprise Technology Analyst Entry…

    Sacramento Municipal Utility District (Sacramento, CA)
    …the job include configuring SAP, and other enterprise applications, to support system modifications and enhancements; provide technical consultation to the business ... close supervision, performs the more basic business processes and technical support utilizing SMUD's various enterprise and other integrated technology solutions in… more
    Sacramento Municipal Utility District (08/08/25)
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  • Staff R&D Engineer - Sustaining

    Stryker (Irvine, CA)
    …venous and other vascular diseases through purpose-driven innovation. As a fast-growing medical device company, we develop breakthrough technologies that treat ... supports and leads project teams in the development of medical device products - this includes writing...management, per the Quality Management System. + Identify and support the creation of or improvements to procedures, policies,… more
    Stryker (08/29/25)
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  • Sr Analyst - Global Trade Compliance…

    Cardinal Health (Sacramento, CA)
    …pharmaceuticals) preferred + 2+ years of experience in classification within the medical device or pharmaceutical industry preferred + Customs Broker's license ... Origin Determinations and FTA eligibility requirements. + Familiarity with medical device and pharmaceutical regulations (eg, FDA...offers a wide variety of benefits and programs to support health and well-being. + Medical , dental… more
    Cardinal Health (08/22/25)
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  • Staff Software Quality Engineer

    J&J Family of Companies (Santa Clara, CA)
    …IEC62304), regulations (eg 21 CFR Part 820, 21 CFR Part 11, European Medical Device Regulation (MDR), and applicable guidance. + Provide Quality representation ... and validation. + 4 years' experience in a quality role within the medical device , aerospace/defense or similarly regulated industry. + Strong verbal and… more
    J&J Family of Companies (08/20/25)
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  • Quality Engineer, Design Control

    Hologic (San Diego, CA)
    …environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR 820, ISO 13485 as well as CE ... FDA, ISO, and other IVD regulations. You will also support the company's quality system activities and design comply...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
    Hologic (07/03/25)
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  • CQV Engineers/Specialists - Open Applications

    VTI Life Sciences (Los Angeles, CA)
    …ambitious engineers looking to accelerate their careers in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more
    VTI Life Sciences (06/24/25)
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  • Service Desk Agent

    Cayuse Holdings (Sacramento, CA)
    …and logging all customer interactions for escalated matters. + Mobile telephony and device support . + Video Conference Unit Troubleshooting. + IP Telephony setup ... user accounts and setting permissions. + Provide end user device management and support , including desktops, laptops,...**Our Commitment to you / overview of benefits** + Medical , Dental and Vision Insurance; Wellness Program + Flexible… more
    Cayuse Holdings (08/26/25)
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  • Service Desk Agent

    Cayuse Holdings (Sacramento, CA)
    …and log all customer interactions for escalated matters + Mobile telephony and device support + Video Conference Unit Troubleshooting + IP Telephony setup ... user accounts and setting permissions + Provide end user device management and support , including desktops, laptops,...**Our Commitment to you / overview of benefits** + Medical , Dental and Vision Insurance; Wellness Program + Flexible… more
    Cayuse Holdings (07/31/25)
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  • Product Quality Assurance Analyst III

    Abbott (Alameda, CA)
    medical devices, customer complaints, and product nonconformances. Prior experience in the medical device industry and/ or quality systems are required. + ... working knowledge of FDA Code of Federal Regulations as it applies to medical device manufacturing, including cGMP, ISO14971, as well as complaint handling… more
    Abbott (08/08/25)
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  • Director, Product Security MedTech

    J&J Family of Companies (Irvine, CA)
    …compliance, cybersecurity incident response and the processes and procedures that support these initiatives. Additional responsibilities will include, but not be ... secure communications (eg TLS/mTLS). + Oversee security integration across medical devices, software, mobile applications, embedded devices, and cloud environments… more
    J&J Family of Companies (08/28/25)
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