• Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... 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)
    …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... 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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  • Associate Principal Scientist, Device

    Merck (Rahway, NJ)
    …Factor Engineering, Inventory Control System, Inventory Management, Mechanical Testing, Medical Device Quality Systems, Negotiation, Project Management, Quality ... with a strong background in digital/data automation to support the Device Development & Technology (DD&T) organization within the Pharmaceutical Sciences and… more
    Merck (09/12/25)
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  • Clinical Data Science- Lead Biostatistician

    J&J Family of Companies (Irvine, CA)
    …or related quantitative field. + Minimum of 6 years of relevant experience in clinical research within Medical Device or Pharmaceuticals, with demonstrated ... will help patients on their journey to wellness. **About the Role:** The ** Clinical Data Science - Lead Biostatistician** will serve as a technical expert within… more
    J&J Family of Companies (09/13/25)
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  • Cardiac Device Monitor

    HonorHealth (AZ)
    …and urgent care services, a cancer care network, outpatient surgery centers, clinical research, medical education, a foundation, an accountable care ... websites, analysis and management of transmission, entering in the electronic medical record (EMR), maintaining the data integrity with the system, patient… more
    HonorHealth (08/02/25)
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  • Product Surveillance Tech I ( Medical

    US Tech Solutions (North Chicago, IL)
    …Code complaint information according to procedures. + Assess incoming documentation, including clinical forms and medical information, for complaint data and ... with one to two years previous experience** in customer service or clinical setting or equivalent combination of education and experience. + **Customer service… more
    US Tech Solutions (07/18/25)
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  • Lead Clinical Data Analyst

    J&J Family of Companies (Warsaw, IN)
    …or related discipline (required), with at least 6 years of system support in clinical research within Medical Device or Pharmaceuticals + Experience with ... as well as other relevant processes + Represent the Medical Devices Sector on Enterprise or cross-sector Clinical... Medical Devices Sector on Enterprise or cross-sector Clinical System teams (as needed) + Assist with the… more
    J&J Family of Companies (09/03/25)
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  • Senior Medical Device Software…

    Medtronic (Newton, MA)
    …user-friendly interfaces that enhance the usability and functionality of our advanced medical devices. The Senior Software Engineer will be a key player in ... components. Experience with regulatory compliance and security protocols specific to medical software (eg, HIPAA, FDA regulations) is preferred but not required.… more
    Medtronic (08/29/25)
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  • Staff Clinical Engineer

    GE HealthCare (Cleveland, OH)
    …degree highly preferred + 10+ years of relevant industry experience; strong clinical knowledge required; medical device development experience preferred ... imaging software to standardize your workflow and simplify increasingly complex clinical scenarios. Leading global healthcare organizations use MIM(R) to give… more
    GE HealthCare (09/06/25)
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  • Director Reg Affairs - Structural Heart…

    Actalent (St. Paul, MN)
    Director of Regulatory Affairs Structural Heart | Medical Device | Relocation Offered Job Description We are seeking an experienced Director of Regulatory ... proven track record in leading regulatory strategy and submissions for Class III medical devices. + Hands-on experience with IDE Products / PMA submissions, FDA… more
    Actalent (09/12/25)
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