• Principal Member of Technical Staff…

    Oracle (Tallahassee, FL)
    …you will be a key contributor to the development of and governing the software architecture and compliance framework for regulated medical devices. This role ... adoption of compliant SDLC processes and tooling. Deep understanding of medical device software regulations and standards along with a proven experience defining… more
    Oracle (11/25/25)
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  • Software Development Engineer…

    Philips (Gainesville, FL)
    …interventional procedures. **Your role:** + Design and develop **high-quality, feature-driven software ** for advanced medical imaging systems using modern ... in medical imaging or other regulated environments. + Experience developing software for ** medical imaging systems** , including modalities, image fusion,… more
    Philips (12/24/25)
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  • Staff Software Design Quality Engineer

    Stryker (Orlando, FL)
    …(FDA, TGA, EUMDR, IT). + Engage in design and development activities for both medical and non- medical software , including SaMD, MDDS, and AI/ML solutions. ... **Staff Software Design Quality Engineer** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or … more
    Stryker (10/30/25)
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  • Staff Software Quality Engineer, Post…

    Stryker (Orlando, FL)
    …performance, and drive continuous improvement for both regulated and non-regulated software medical products after market release. **Workplace Flexibility & ... Software Quality Engineer, Post Market** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD)/ Software more
    Stryker (01/06/26)
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  • Senior Software Quality Engineer, Design…

    Stryker (Orlando, FL)
    …is hiring a **Senior Software Quality Engineer, Design Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical ... Device (SiMD) or Software in a Medical Device (SiMD) to execute on Digital Health projects...device regulations (820, IEC 62304/82304, 60601), with experience in Software as a Medical Device (SaMD), … more
    Stryker (01/09/26)
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  • CPQ, Medical Informatics Marketing Manager…

    Fujifilm (Tallahassee, FL)
    …enterprise quotes. + Understand the specialized requirements for quoting regulated medical software , hardware, and consulting; ensuring accurate compliance, ... **Position Overview** The CPQ Product Marketing Manager, Medical Informatics (MI), manages our go-to CPQ market...CPQ platform enhancements and relevant trends in healthcare enterprise software solutions. + Ensure that the CPQ platform decisions… more
    Fujifilm (12/30/25)
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  • Principal SaMD Quality & Compliance Manager - AI…

    Oracle (Tallahassee, FL)
    …strategically and tactically. Preferred Experience + Background in digital health, AI/ML medical software , or imaging platforms. + Experience with CE Mark ... and mature our quality systems and regulatory readiness for AI-enabled Software as a Medical Device (SaMD) and digital health solutions. This role sits within… more
    Oracle (01/10/26)
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  • Medical Receptionist

    Robert Half Office Team (Miami, FL)
    …and patient-focused attitude + Proficiency in Microsoft Office (Outlook, Word, Excel) and medical software + Strong organizational skills and attention to detail ... Description We are seeking a professional and compassionate Medical Receptionist to manage front desk operations in... Receptionist to manage front desk operations in a medical office. This role is ideal for someone who… more
    Robert Half Office Team (01/10/26)
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  • Clinical Product Manager - Medical Device…

    Oracle (Tallahassee, FL)
    …Knowledge of ISO 14971, IEC 62366, EU MDR/IVDR, and FDA guidance related to medical device software (SaMD). . Strong understanding of clinical risk, safety ... audits (EU MDR, FDA 510(k), etc.). . Experience working with AI-driven medical device applications or software as a medical device (SaMD). . Familiarity with… more
    Oracle (12/22/25)
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  • Clinical Product Manager - Medical Device…

    Oracle (Tallahassee, FL)
    …Knowledge of ISO 14971, IEC 62366, EU MDR/IVDR, and FDA guidance related to medical device software (SaMD). . Strong understanding of clinical risk, safety ... audits (EU MDR, FDA 510(k), etc.). . Experience working with AI-driven medical device applications or software as a medical device (SaMD). . Familiarity with… more
    Oracle (11/25/25)
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