• 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, ... (eg, Statistical Analysis, NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory ... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management… more
    US Tech Solutions (07/18/25)
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  • Senior Specialist, Drug/ Device Combination…

    Merck (Sacramento, CA)
    medical devices and combination products globally. * Experience in design controls, device risk management, medical device , complex combination product ... are the cornerstone of decisions and expectations * Lead technical investigations of medical device and combination product needs for commercial products *… more
    Merck (08/29/25)
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  • 1st Shift Medical Device Assembler

    Aerotek (Irvine, CA)
    **Job Title: 1st Shift Medical Device Assembler** Job Description We are seeking a dedicated Assembler I to join our team on a 12-18 month contract. This role ... processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +...or equivalent. Additional Skills & Qualifications + Experience in medical device assembly. + Cleanroom experience. +… more
    Aerotek (08/29/25)
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  • Medical Device Assembler

    Aerotek (Irvine, CA)
    ** Medical Device Assembler I - 1st Shift** **Job Description** We are seeking a dedicated Assembler I who will be responsible for assembling and testing ... processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +...the shift. **Additional Skills & Qualifications** + Experience in medical device assembly. + Cleanroom experience is… more
    Aerotek (08/23/25)
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  • 2nd Shift Medical Device Assembler

    Aerotek (Irvine, CA)
    **Job Title: 2nd Shift Medical Device Assembler** **Job Description** Join a dynamic team as a 2nd Shift Assembler where you'll play a crucial role in the ... School Diploma or equivalent. + Familiarity with cleanroom environments is beneficial. + Medical device assembly experience is preferred. **Why Work Here?** Be… more
    Aerotek (08/21/25)
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  • Medical Device Production Training…

    Kelly Services (Santa Clara, CA)
    …Training Specialist** . This is a temp-hire contract with one of our Global Medical Device Robotics & Digital Solutions clients, located in **Santa Clara, CA.** ... this group you will be eligible for 50% paid Medical & Dental, a 401K plan, and a variety...Coordinates the performance of audits to assess compliance with quality and regulatory requirements. Demonstrates Leadership Imperatives… more
    Kelly Services (08/08/25)
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  • 2nd Shift Medical Device Assembler

    Aerotek (Irvine, CA)
    …+ HS Diploma or Equivalent. Additional Skills & Qualifications + Experience in medical device assembly is preferred. + Cleanroom experience is advantageous. + ... a crucial role in the assembly and testing of medical devices. This position requires flexibility with shift hours...processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +… more
    Aerotek (08/29/25)
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  • Project Manager, Device Engineering

    Gilead Sciences, Inc. (Foster City, CA)
    …goals, and results to team members across functions and departments, including device development, packaging, quality , regulatory affairs and manufacturing. ... + Experience in the pharmaceutical or biotechnology industry is preferred + Medical device or combination product experience is preferred + PMP certification is… more
    Gilead Sciences, Inc. (08/29/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory ... 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)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Pleasanton, CA)
    …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory ... 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)
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