• Sr. Scientist Clinical Research

    Abbott (Santa Clara, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs or Clinical Science, Risk Management, Clinical… more
    Abbott (06/21/25)
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  • Staff Java Developer

    Abbott (Sylmar, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... skills and a passion for staying updated with the latest industry trends. + Medical device product development knowledge a plus + Ability to independently… more
    Abbott (08/08/25)
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  • Scientist II (Formulation Development)

    Astellas Pharma (South San Francisco, CA)
    …organize necessary activities, plan studies and obtain sufficient data. + Evaluate new medical devices or container-closures for local injection products + Lead ... world. We are committed to turning innovative science into medical solutions that bring value and hope to patients...for clinical use. + Conduct in-use stability and delivery device compatibility studies to ensure the quality more
    Astellas Pharma (08/08/25)
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  • Principal Systems Engineer

    Abbott (Pleasanton, CA)
    …integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (07/18/25)
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  • Specialist, Clinical Safety

    Terumo Neuro (Aliso Viejo, CA)
    …review, investigation, and assessment of adverse events. 5. Class III medical device safety experience. **External-Facing Title:** Specialist, Clinical Safety ... milestones and to provide regular progress updates. + Support clinical science and regulatory affairs functions by utilizing medical expertise to provide input… more
    Terumo Neuro (07/12/25)
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  • Senior Manager Medical Affairs

    Abbott (Santa Clara, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... work with investigators and internal cross-functional partners to ensure high- quality studies meeting medical /scientific/business needs. **What You'll Work… more
    Abbott (08/30/25)
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  • Director of API Manufacturing

    Kelly Services (South San Francisco, CA)
    …advance your career, join us as we pioneer progress in the biotechnology and medical device industries. **Workplace:** Hybrid, onsite in South San Francisco, CA, ... of CMC, you'll be instrumental in overseeing API process scale-up, regulatory strategy, and operational excellence required for clinical and commercial success.… more
    Kelly Services (08/29/25)
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  • Lead Electrical Engineer (Medium Voltage)

    WSP USA (San Diego, CA)
    …grounding touch and step potentials, short circuit study, protective device coordination, one-line diagram development, protective relaying, and substation ... and clients. + Develop and incorporate advanced technologies, monitoring devices , building materials, modeling techniques, design requirements, load calculations,… more
    WSP USA (06/24/25)
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  • Medical Equipment Technician

    Agiliti Health (Redlands, CA)
    … equipment management experts who proudly serve hospitals and healthcare facilities to ensure quality medical equipment is in the right place at the right time ... maintenance, calibration, and repair service on a variety of medical devices including medical beds,...promptly to ensure complete documentation for billing and required regulatory compliance. + Communicate with clinical staff on the… more
    Agiliti Health (08/08/25)
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  • R&D Software Engineer III

    ManpowerGroup (San Diego, CA)
    …preferred). + 10+ years of experience in software/system development, preferably in connected device or medical device environments. + Strong Agile ... understanding of OAuth 2.0, OpenID, TLS, and cybersecurity. **Preferred:** + Experience with medical device regulations (ISO 13485, IEC 62304, FDA 21 CFR Part… more
    ManpowerGroup (07/16/25)
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