• Sr Java Full Stack Engineer

    Abbott (San Diego, CA)
    …debuggers, unit test frameworks) + Knowledge of design controls and regulations for medical device development is a plus + Understanding of quality software ... visual modeling, multi-threading, formal development methodologies, and source code management + Medical device product development knowledge is a plus +… more
    Abbott (11/06/25)
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  • Driver Route NonCDL-Med

    WM (Vernon, CA)
    …a US based business-to-business services company and leading provider of compliance -based solutions that protects people and brands, promotes health and well-being, ... ago, we have grown from a small start-up in medical waste management into a leader across a range...addition, all vehicles are equipped with ELD (electronic logging device ) and GPS (global positioning system). **Schedule and Location:**… more
    WM (10/18/25)
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  • Staff R&D Engineer - Sustaining & Model…

    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 ... Staff R&D Engineer supports and leads project teams in the development of medical device products - this includes writing or verifying specifications, developing… more
    Stryker (10/04/25)
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  • Electric Program Manager

    Silicon Valley Power (Santa Clara, CA)
    …term strategic and operational plans, monitor related legislation, regulations, reporting and compliance and serve as the liaison to various stakeholder groups. The ... works closely with other Division personnel including Plant Engineer, Compliance Manager, and administrative staff and reports directly to...Account funds may be used to pay for qualified medical expenses after separation from the City and after… more
    Silicon Valley Power (11/19/25)
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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 ... team member on New Product Development projects to ensure compliance with design controls, as well as identify and...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
    Hologic (11/21/25)
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  • Equipment Calibration and Preventive Maintenance…

    Cordis (Irvine, CA)
    …organized work approach. **Preferred:** + Experience in Class IIb or III implantable medical device manufacturing. + Previous experience in a cleanroom or ... the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery… more
    Cordis (11/12/25)
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  • Multicraft Technician (Electrician & HVAC)

    Mentor Technical Group (Millbrae, CA)
    …knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... or equipment maintenance role in a regulated industry (pharmaceutical, biotech, or medical device preferred). + EPA Universal Certification (Section 608). +… more
    Mentor Technical Group (11/07/25)
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  • Quality Engineer

    Hologic (San Diego, CA)
    …you an aspiring quality professional looking to start or grow your career in the medical device industry? At Hologic, we are seeking a **Quality Engineer** to ... support validation efforts, risk management, and compliance within our Quality Management System. In this role,...**Experience:** + 0-2 years of experience in a diagnostic, medical device , biotech, or pharmaceutical company. +… more
    Hologic (10/02/25)
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  • Manufacturing Technician

    Kelly Services (Petaluma, CA)
    …for a **skilled Manufacturing Technician** with 3 to 5 years of experience in medical device or biopharma manufacturing. This role is ideal for someone who ... **What You Will Do** * Build, assemble, and test medical device components according to SOPs and...tasks * Keep production areas clean, organized, and in compliance with safety and GMP standards * Work closely… more
    Kelly Services (12/03/25)
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  • Assoc Endoscopic Repair Tech

    Fujifilm (Cypress, CA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field....held religious belief or other legally required exemption._ _In compliance with the ADA Amendments Act, should you have… more
    Fujifilm (12/02/25)
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