• Principal Process Engineer

    Medtronic (Northridge, CA)
    …Develop & utilize technical & wet lab skills associated with medical device coatings/deposition & relevant fabrication processes + Utilize design of experiments ... support Bill Of Materials (BOM) + Oversee & coordinate device build, sterilization, and testing + Resolve non-compliance issues...job, the employee is regularly required to be independently mobile . The employee is also required to interact with… more
    Medtronic (10/04/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    …duties as assigned or required. **To Be Successful in This Role** + **Medical Device Experience:** Minimum of 4 years of relevant experience in medical device ... a minimum of 2 years of experience in medical device regulatory affairs is a plus. + **Regulatory Knowledge:**...job, the employee is regularly required to be independently mobile . The employee is also required to interact with… more
    Medtronic (09/30/25)
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  • Principal R&D Engineer

    Medtronic (San Diego, CA)
    …for commercial launch. The individual will leverage strong knowledge of medical device regulations and experience with quality management systems to drive successful ... outcomes. The ideal candidate for this position has experience in medical device design, process development, and characterization testing and has a strong… more
    Medtronic (09/25/25)
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  • Principal Regional Field Educator, CAS

    Medtronic (CA)
    …tenured field team + Leads coordination of new-hire training with accountability to hiring manager (CSM or RM) + Responsible for new hire sign-off + Delivers new ... in the Cardiac Ablation, Cardiac Rhythm, or Implantable Medical Device Industry OR + Advanced Degree in Engineering or...this job, the employee regularly required to be independently mobile + Ability to travel with overnight stay up… more
    Medtronic (10/04/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (Los Angeles, CA)
    …and 4+ years of regulatory affairs experience, preferably with medical device submissions, registrations or advertising and promotional review. OR Advanced Degree ... and 2+ years of regulatory affairs experience, preferably with medical device submissions, registrations or advertising and promotional review. **Nice to Have**… more
    Medtronic (10/01/25)
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  • Senior Biomedical Engineer/Biocompatibility

    Medtronic (Northridge, CA)
    …ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive biocompatibility assessments, ... + Provide technical documentation concerning biological assessments of material and device safety per ISO 10993-1. Conduct biocompatibility impact assessment for… more
    Medtronic (09/25/25)
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  • R&D Engineering Intern - Summer

    Medtronic (Irvine, CA)
    …support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; ... analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. + Assumes responsibility for … more
    Medtronic (08/02/25)
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  • IT Asset Technician

    Cupertino Electric (San Jose, CA)
    …ensuring proper configuration and setup. **Lifecycle Management:** + Support laptop and mobile device refresh, upgrade, and replacement initiatives. + Perform ... **Posting Title:** IT Asset Technician **Reports To:** Manager , IT Asset Management **Location:** San Jose, California...are entered into the inventory system. + Deploy laptops, mobile devices, peripherals, and other IT equipment to employees,… more
    Cupertino Electric (09/02/25)
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  • Clinical Specialist CRM - Los Angeles / Downey

    Medtronic (Los Angeles, CA)
    …online and field-based training + Performs checks/interrogations of all CRM medical device systems post sign-off + Supports implants of all CRM products post ... + Thorough working knowledge of medical terminology and the medical device industry + Proven ability to build/maintain positive relationships with peers… more
    Medtronic (10/01/25)
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  • Principal MDR - Vigilance Specialist

    Medtronic (Los Angeles, CA)
    …transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse reaction data ... meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements by...with our team and the workplace environment. Your direct manager will be your point of contact to help… more
    Medtronic (09/30/25)
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