• Sr Specialist, Clinical Trial Quality Assurance

    Terumo Neuro (Aliso Viejo, CA)
    …(SOPs), regulations, standards, good clinical practices, and guidelines applicable to the medical device industry to contribute to overall quality and regulatory ... standards, good clinical practices, and guidelines applicable to the medical device industry. + Identify gaps and...5. Advanced working knowledge of QA principles including Quality Risk Management (QRM), Critical Thinking, and Quality… more
    Terumo Neuro (06/17/25)
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  • Staff Engineer, Program/Project Management

    Celestica (San Jose, CA)
    …Skills + **DESIGN PM** : PMP Certified, Agile PM Methodologies, Managing Projects, Risk Management , Creating Project Plan, PM Tools, Contract Management , ... Creation, Test Plan Creation, PMP Certified, Agile PM Methodologies, Managing Projects, Risk Management , Creating Project Plan, PM Tools, Contract Management more
    Celestica (08/30/25)
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  • Principal Product Manager (Zero Trust Identity)

    Palo Alto Networks (Santa Clara, CA)
    …Identity Engine and User-ID, identifying a user on a network + Authorization: Management of users, groups, devices , and attributes across on-premise and cloud ... Identity security: user-based risk modeling with security Risk and posture management across Identity providers,...User-ID, identifying a user on a network + Authorization: Management of users, groups, devices , and attributes… more
    Palo Alto Networks (08/09/25)
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  • Regulatory Affairs Manager - Heart Failure…

    Abbott (Pleasanton, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Ability to work in a highly… more
    Abbott (06/16/25)
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  • Lead Test Automation Architect (Cloud, Web,…

    Abbott (Pleasanton, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... CA** location in the Heart Failure business within Abbott Medical Devices . In Abbott's Heart Failure (HF)...and implement comprehensive test automation strategies for Abbott's next-generation medical device software portfolio (Class II and… more
    Abbott (07/16/25)
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  • Quality Engineer

    Abbott (Temecula, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... serve people in more than 160 countries. **About Abbott** For years, Abbott's medical device businesses have offered technologies that are faster, more… more
    Abbott (06/24/25)
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  • Director, Human Factors Engineering

    Abbott (Milpitas, CA)
    …other scientific or engineering field. + 10-15 years of management and technical management experience in the medical device industry with minimum 5 ... the above disciplines. + Experience in medical device development especially in system engineering and/or risk... device development especially in system engineering and/or risk management + Working knowledge of cardiac… more
    Abbott (08/08/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + You ... fit if:** + You have 15+ years of R&D leadership developing and launching medical devices and a Bachelor's or advanced degree in Engineering (Biomedical,… more
    Philips (08/21/25)
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  • Sr Systems Verification Engineer

    Globus Medical, Inc. (Redwood City, CA)
    …3 years with a PhD - related experience with development or verification in the medical device industry. (class III medical device experience preferred). ... At Globus Medical , we move with a sense of urgency...and an understanding of embedded firmware strong desired. + Risk management ( risk analysis, FMEA,… more
    Globus Medical, Inc. (08/26/25)
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  • Regulatory Compliance - Senior Analyst

    Kelly Services (Irvine, CA)
    …* At least 5 years of experience in a Quality, Manufacturing or Engineering function in medical device industry * At least 5 years of experience in a Quality, ... Manufacturing or Engineering function in medical device industry * Experience with MDSAP...CFR Part 820 QSR, ISO 13485, Brazil GMP, Canada Medical Devices Regulations SOR 98-282, Japan's MHLW… more
    Kelly Services (08/22/25)
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