• Manager, Strategic Accounts- Shockwave- Remote-…

    J&J Family of Companies (San Francisco, CA)
    …moral character while professionally representing the company. + Comply with all corporate compliance, FDA , medical device , quality standards and ethics. ... + Must not be debarred by FDA for work in any Medical Device business. + Ability to work in a fast-paced environment while managing multiple priorities.… more
    J&J Family of Companies (08/30/25)
    - Related Jobs
  • Quality Engineer II (Onsite)

    Cordis (Santa Clara, CA)
    …of education and experience preferred + Expertise in the FDA and International Medical Device Quality System Regulations and ISO 13485 + Six Sigma, ... + Ability to comprehend principles of engineering, chemistry, polymers, physiology, and medical device use. **REQUIRED KNOWLEDGE, SKILLS, ABILITIES** + Excellent… more
    Cordis (08/07/25)
    - Related Jobs
  • Quality Engineer (Electromechanical…

    AbbVie (Pleasanton, CA)
    …discipline. Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, ... GD&T + performing daily assigned tasks in compliance with FDA 's Quality System Regulation (QSR), ISO 13485,...MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes… more
    AbbVie (06/26/25)
    - Related Jobs
  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification, ... NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA ,... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management… more
    US Tech Solutions (07/18/25)
    - Related Jobs
  • Staff Engineer, Quality (New Products)

    Terumo Neuro (Aliso Viejo, CA)
    …and data analysis. 3. Demonstrated command and knowledge of FDA and ISO medical device quality system requirements. 4. Proven experience in statistical ... quality engineering projects to support the manufacturing of medical devices. Work with Manufacturing and R&D in leading...design verification, and design validation. 2. Strong knowledge of medical device design control process. 3. Ability… more
    Terumo Neuro (06/19/25)
    - Related Jobs
  • Medical Device Assembler

    Aerotek (Irvine, CA)
    ** Medical Device Assembler** Job Description + Join our team as an Assembler responsible for the production of high- quality medical devices, primarily in ... working with chemicals + 1+ year of experience in medical device manufacturing + Experience with or...Join a forward-thinking team poised for growth with anticipated FDA approval in the US next year. Be a… more
    Aerotek (08/29/25)
    - Related Jobs
  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to… more
    AbbVie (06/19/25)
    - Related Jobs
  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Pleasanton, CA)
    FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...work collaboratively with a team to design and develop medical products from initial concept through the transfer to… more
    AbbVie (06/19/25)
    - Related Jobs
  • Director Program Management ( Medical

    Danaher Corporation (West Sacramento, CA)
    …Microbiology Team via PPG, and functional leaders. + Drive achievement of Quality , Cost, and Delivery (QCD) metrics. + Identify risks and implement countermeasures ... preference for 2-5 years in program/project management. + Experience in FDA -regulated/IVDR environments strongly preferred. + PMP or equivalent certification highly… more
    Danaher Corporation (08/28/25)
    - Related Jobs
  • Medical Devices Software Quality

    US Tech Solutions (San Bruno, CA)
    …standards and corporate requirements. **Regulatory Compliance:** 1. Ensure compliance with US FDA Quality System Regulations, ISO 13485, and integration of best ... practices from the medical device industry. **Documentation and Support:** 1....software development lifecycle, including familiarity with SDLC processes and Quality Management Systems (QMS) compliant with US FDA more
    US Tech Solutions (07/18/25)
    - Related Jobs