• Director, Human Factors Engineering

    Abbott (Milpitas, CA)
    …design, user error analysis, usability and validation testing. + Extensive knowledge of entire medical device development process from needs definition ... + Ph.D. degree in one of the above disciplines. + Experience in medical device development especially in system engineering and/or risk management + Working… more
    Abbott (08/08/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Sacramento, CA)
    …to be an integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, ... responsible for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and… more
    Fujifilm (08/08/25)
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  • Technical Director, BAW Device

    Skyworks (Irvine, CA)
    Technical Director, BAW Device Development Apply now " Date:Aug 24, 2025 Location: Irvine, CA, US Company: Skyworks If you are looking for a challenging and ... 74982 Description Skyworks Solutions seeks a director of BAW device development who will lead a small...understanding of Bulk Acoustic Wave (BAW) devices and associated process technology. + Experienced in using Finite Element Modeling… more
    Skyworks (07/08/25)
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  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …utilizing expertise in the medical device product development life-cycle, Risk Management, Design/ Process Verification, and Validation. + Supporting ... track record of handling multiple programs and streams of work. + Experience with medical device development standards eg ISO 13485, FDA 21 CFR 820 +… more
    US Tech Solutions (07/18/25)
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  • Associate Sales Consultant - Medical

    IQVIA (San Bernardino, CA)
    …Sales Consultants_** to join our team of field employee's. **Associate Sales Consultant - Medical Device ** If you have ever wondered about the intricacies of ... surgical procedures or considered a career path in medical device sales, this is the role...healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments… more
    IQVIA (08/15/25)
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  • Medical Device Assembler

    Kelly Services (Irvine, CA)
    …to support production demand and new product development . **Position Summary:** As a Medical Device Assembler, you will play a key role in developing and ... Medical Device Assemblers...process instructions to build catheters to meet product development and launch commitments. + Meet catheter manufacturing yield… more
    Kelly Services (08/26/25)
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  • Senior Manager, Regulatory Affairs - Device

    AbbVie (Irvine, CA)
    …CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...the Regulatory Affairs functional areas, Operations, and Research & Development (R&D) organizations. Represents RA Device on… more
    AbbVie (08/27/25)
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  • Sr. Software Development Engineer, Emerging…

    Amazon (Sunnyvale, CA)
    …work in a high-ambiguity, dynamic problem space - - Exposure to cross-platform development , device integration, or consumer hardware - - Demonstrated ability to ... Description We are looking for an experienced and motivated Sr. Software Development Engineer to join Amazon's Smart Eyewear initiative on the Emerging Devices… more
    Amazon (08/16/25)
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  • Quality Specialist ( Medical Device

    Astrix Technology (Irvine, CA)
    **Quality Specialist ( Medical Device )** Quality Control Irvine, CA, US Pay Rate Low: 32.00 | Pay Rate High: 36.00 + Added - 26/08/2025 Apply for Job Exciting ... Quality Engineer Specialist development opportunity to work for a global leader dedicated...regulations (21 CFR 820/803), ISO 13485 + Experience with medical device complaint handling and regulatory reporting… more
    Astrix Technology (08/27/25)
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  • Quality Engineer (Electromechanical Medical

    AbbVie (Pleasanton, CA)
    …(QSR), ISO 13485, ISO 14971, MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & + ... Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year… more
    AbbVie (06/26/25)
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