• Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance . These studies will be conducted at the Stanford ... disease areas including: Epilepsy, Neuorimmunology/Multiple Sclerosis, Alzheimers, Autonomic Disorders, Device Neurosurgery, Stem Cell Neurosurgery, Headache, Radiology, Parkinson's and… more
    Stanford University (08/07/25)
    - Related Jobs
  • Sr. Product Security Engineer (San Diego, CA…

    Abbott (San Diego, CA)
    …Your work will support threat modeling, risk assessments, vulnerability management, and regulatory compliance , helping ensure our products are secure and ... into the product lifecycle** , ensuring our devices meet regulatory requirements and protect patient safety. **What You'll Work...field. + 6+ years of experience in embedded systems, medical device development, or product cybersecurity. +… more
    Abbott (08/01/25)
    - Related Jobs
  • Staff Engineer Research and Development (Onsite)

    Cordis (Santa Clara, CA)
    …understanding of cardiovascular catheter technologies and procedures. + Applies comprehensive medical device engineering knowledge and a thorough understanding ... of concepts, principles, and technical capabilities to achieve design realization of medical devices. + Plans and develops engineering projects concerned with unique… more
    Cordis (07/24/25)
    - Related Jobs
  • Semiconductor Process Engineer

    Teledyne (Camarillo, CA)
    …development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals ... with the established manufacturing procedures and work instructions, and in compliance with environmental and safety regulations and AS9100 quality standard. +… more
    Teledyne (08/09/25)
    - Related Jobs
  • R&D Software Engineer III

    ManpowerGroup (San Diego, CA)
    …preferred). + 10+ years of experience in software/system development, preferably in connected device or medical device environments. + Strong Agile ... understanding of OAuth 2.0, OpenID, TLS, and cybersecurity. **Preferred:** + Experience with medical device regulations (ISO 13485, IEC 62304, FDA 21 CFR Part… more
    ManpowerGroup (07/16/25)
    - Related Jobs
  • Account Director/ Sr Account Director Business…

    ThermoFisher Scientific (Carlsbad, CA)
    …organizational expertise, and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a proven track record ... key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in...+ Awareness of regulatory landscape, including understanding regulatory bodies, compliance requirements, and any changes… more
    ThermoFisher Scientific (07/03/25)
    - Related Jobs
  • Clinical Research Manager - JJMT Electrophysiology

    J&J Family of Companies (Irvine, CA)
    …+ Experience with budget planning, tracking and control is required. + Medical Device experience is required. **Preferred Education & Skills/Experience:** + ... to execute and manage company sponsored clinical trials, ensuring monitoring compliance with timelines and study milestones for JNJ MedTech - Electrophysiology… more
    J&J Family of Companies (08/29/25)
    - Related Jobs
  • Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …data, administration of neuropsychological testing batteries, maintenance of study regulatory compliance , and patient recruitment. Extensive training will ... in pursuing graduate or medical school, and/or interested in bioinformatics or medical device industry. This CRCA position is a full-time position and a… more
    Stanford University (08/19/25)
    - Related Jobs
  • Staff Quality Auditor

    Abbott (Alameda, CA)
    …10 yrs of work experience will be considered. + Min 10 years of experience in the medical device industry + Min 8 years auditing per ISO and/or FDA standards. + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (06/29/25)
    - Related Jobs
  • Staff Software Quality Engineer

    J&J Family of Companies (Santa Clara, CA)
    …IEC62304), regulations (eg 21 CFR Part 820, 21 CFR Part 11, European Medical Device Regulation (MDR), and applicable guidance. + Provide Quality representation ... and validation. + 4 years' experience in a quality role within the medical device , aerospace/defense or similarly regulated industry. + Strong verbal and… more
    J&J Family of Companies (08/20/25)
    - Related Jobs