• Principal Quality Mfg Engineer, Selution

    Cordis (Irvine, CA)
    …Stay up-to-date with regulatory requirements, standards, and guidelines relevant to the medical device industry and ensure that manufacturing processes adhere to ... Biomedical Engineering, or a related field. + At least 8 years in medical device production development + Previous experience with product lifecycle (post… more
    Cordis (08/14/25)
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  • Project Manager, Medical Devices

    Abbott (Pleasanton, CA)
    …cross-functional project teams** to drive supplier quality initiatives, ensuring alignment with medical device regulatory standards (eg, FDA, ISO 13485). + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (08/14/25)
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  • Sr. Sourcing Specialist

    Caldera Medical (Westlake Village, CA)
    …by 2027! Who is Caldera Medical ? Caldera Medical is a growth stage medical device company dedicated to improving the quality of life for women. In 2018, ... Sourcing Specialist 100% ONSITE - Westlake Village, California Caldera Medical 's Mission - To Improve the Quality of Life...in quality, service, and cost. * Apply market insights, risk assessments, and cost analysis to sourcing decisions. *… more
    Caldera Medical (08/27/25)
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  • Senior Development Quality Manager

    Abbott (Menlo Park, CA)
    …agency regulations. **What You'll Work On** + Provide leadership in direct support of medical device manufacturing. + Management and development of Quality ... or mechanical engineering preferred. + Class III or II medical device experience (catheter experience preferred). +... reduction, and cost containment. + Deep understanding of risk management in design, manufacturing and post-market… more
    Abbott (08/20/25)
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  • Regulatory Affairs Manager - Heart Failure…

    Abbott (Pleasanton, CA)
    …and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Ability to work in a highly ... for US, EU (EU MDR), and other international geographies. + Experience with medical device software requirements and software regulations. + Ability to identify… more
    Abbott (06/16/25)
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  • Lead Product Manager, ATO, Identity Intelligence…

    DoorDash (San Francisco, CA)
    …at scale. + Launch real-time fraud defenses that leverage behavioral biometrics, device intelligence, and machine learning-based risk scores. + Unify fraud ... the platform. You'll partner cross-functionally with Engineering, Data Science, Risk Operations, and Customer Experience teams to build and...you because + You have 7+ years of product management experience, with a proven track record of owning… more
    DoorDash (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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  • Quality, Training, and Innovation Programs Manager

    CalSTRS (Sacramento, CA)
    …includes the teams responsible for the Employer Services Division's quality and risk management programs, internal and external training programs, and innovation ... and Development Staff Services Manager I, the Quality and Risk Management Staff Services Manager I, and...+ Flexible work hours + Remote work options + Medical benefits, including health, dental and vision insurance +… more
    CalSTRS (08/24/25)
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  • Foundry Technology Principal Engineer

    Skyworks (Irvine, CA)
    …fast-paced environment with a strong focus on global collaboration, minimal layers of management , and the freedom to make meaningful contributions in a setting that ... products. + Collaborate with internal design, product, reliability, and program management teams to define new technology introduction (NTI) scope, including… more
    Skyworks (08/27/25)
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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 Audits, health authorities and notified bodies * Working knowledge of … more
    Kelly Services (08/22/25)
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