• Principal Enterprise Architect

    Fujifilm (Springfield, IL)
    **Position Overview** The Principal Enterprise Architect is the technical liaison between development and the various Medical Informatics departments. Principal ... IT infrastructure design and deployment, medical imaging industry in general and clinical environment workflow. In addition to technical expertise, HCUS relies on… more
    Fujifilm (09/24/25)
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  • Senior Principal , Regulatory Affairs…

    Danaher Corporation (Deer Park, IL)
    …diagnostics specifically Companion Diagnostics and digital pathology in the clinical oncology environment. The Senior Principal , Regulatory Affairs ... secure product approvals. + Collaborate cross-functionally and globally with Clinical Affairs, R&D, QA, and Business Development to align regulatory plans with,… more
    Danaher Corporation (10/07/25)
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  • Principal Regional Field Educator, CAS

    Medtronic (IL)
    …plan for educational programs for new and tenured sales representatives and clinical specialists to drive electrophysiology (EP) product procedure across the ... on clinical value + Collaborates to roll out new product training initiatives; new products' indications, troubleshooting/tips and tricks, safety updates -… more
    Medtronic (10/04/25)
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  • Principal Mechanical Engineer, R&D - NPD

    Stryker (Cary, IL)
    As a Principal Mechanical Design Engineer on Stryker's Sage New Product Development team, you will play a pivotal role in designing innovative medical devices ... clinical requirements. + Apply advanced engineering principles to solve cross-functional product challenges and drive innovation across new product more
    Stryker (08/13/25)
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  • Principal Software Engineer

    GE HealthCare (Chicago, IL)
    …more personalized, and more accessible for everyone. From driving the overall clinical research and patient-centric innovation strategy to delivering new digital ... **Job Description Summary** As a Principal Engineer, you will play a pivotal role...organization. You will collaborate closely with architects and technical product managers to translate overarching system architecture and … more
    GE HealthCare (09/23/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (Mettawa, IL)
    …academia required or in a related area such as quality, regulatory, publications, clinical research, or product support/R&D. + 2 years relevant industry ... talent pipeline and considered for future opportunities. About the role: The Principal Medical Writer is responsible for providing writing support and advanced… more
    AbbVie (07/14/25)
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  • Principal Research Scientist I PDS&T

    AbbVie (North Chicago, IL)
    …+ Tech transfer activities for parenteral DP from development scale up to clinical /commercial scale. + Support drug product manufacture at GMP facilities from ... technical projects at all stages of development are included, from phase II clinical through commercial. + Lead cross-functional PDS&T product teams and… more
    AbbVie (09/27/25)
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  • Senior Principal Vascular Therapy…

    Medtronic (Chicago, IL)
    …to the development of a strong team effort **Self-Development and Product Knowledge:** + Develop and maintain comprehensive technical/ clinical knowledge ... you can begin a life-long career of exploration and innovation , while helping champion healthcare access and equity for...+ Develop and execute market development plans to expand product reach and enhance adoption. + Effectively manage expenses… more
    Medtronic (09/18/25)
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  • Principal Strategic Medical Writer…

    AbbVie (Chicago, IL)
    …Tok (https://www.tiktok.com/@abbvie) . Job Description Responsible for leading and writing clinical and regulatory documents for drug and/or device development in ... support of company objectives. Responsibilities: *Independently prepares most clinical and regulatory documents needed for the development of AbbVIe drugs and/or… more
    AbbVie (10/04/25)
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  • Principal Strategic Medical Writer - Device

    AbbVie (Chicago, IL)
    …(https://www.tiktok.com/@abbvie) . Job Description Purpose Responsible for leading and writing clinical and regulatory device and drug documents in support of ... participates in writing documents from study start-up to those that support product approvals (eg briefing books, IND, protocol, CSR, NDA sections, and regulatory… more
    AbbVie (10/04/25)
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