• Technical Program Manager - BADGE Kiosk Hardware

    Oracle (Tallahassee, FL)
    …and scalable processes. + Serve as the escalation authority for device performance, software/firmware issues, and field incidents. + Author roadmaps, investment ... cases, automation strategies, and device standardization documents. **KEY RESPONSIBILITIES:** + Develop, communicate, and...deliver against project milestones and SLAs, ensuring performance and compliance at every stage. + Drive adoption of IoT… more
    Oracle (11/25/25)
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  • Sr Medical Science Liaison, Selution (Mid…

    Cordis (FL)
    …treatments for coronary and peripheral artery diseases. With four Investigational Device Exemptions (IDEs) approved and actively enrolling patients (Coronary ISR, ... SFA, and Peripheral BTK), Cordis is leading the way in delivering transformative medical solutions. At Cordis, we're teammates, not just employees. We embrace an… more
    Cordis (10/17/25)
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  • Sr Medical Science Liaison (Remote)

    Cordis (Miami Lakes, FL)
    …of field based MSL experience and/or 3-5 years of work experience in the medical device or pharmaceutical industry required + Knowledge of the US Healthcare ... Oversee and manage externally sponsored research studies in full compliance with internal procedures. Support the transformation of the...System / medical device industry, including relevant regulations (FDA),… more
    Cordis (10/17/25)
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  • Senior Software Quality Engineer, Design Assurance

    Stryker (Orlando, FL)
    …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD) or Software in a Medical Device (SiMD) ... maintained engineering documentation, including Design History Files, in accordance with medical device regulatory standards. + Demonstrated strong understanding… more
    Stryker (10/22/25)
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  • Staff Software Design Quality Engineer

    Stryker (Orlando, FL)
    …Engineer** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... strong technical skills + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more
    Stryker (10/30/25)
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  • Field Clinical Specialist

    Terumo Medical Corporation (Miami, FL)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... commitment to patient safety and product quality by maintaining compliance with all TMC Quality Systems requirements. This includes...Prior experience as a Field Clinical Specialist with a medical device company is preferred. It is… more
    Terumo Medical Corporation (11/19/25)
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  • Manager, Medical Education (Remote)

    Cordis (Miami Lakes, FL)
    … education, clinical education, or field clinical roles within the medical device or procedural healthcare industry (combined education/experience considered). ... people who keep saving lives. **Responsibilities** **Job Summary** The Medical Education Manageris responsible fordesigning, implementing, and evaluatingcliniciantraining programs… more
    Cordis (10/04/25)
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  • Director, Medical Education (Remote)

    Cordis (Miami Lakes, FL)
    …6+ years of experience in medical education leadership within the medical device industry, with significant exposure to cardiovascular technologies. + ... people who keep saving lives. **Responsibilities** **Job Summary:** The Director of Medical Education will lead and design the next era of world-class cardiovascular… more
    Cordis (10/08/25)
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  • CPQ, Medical Informatics Marketing Manager…

    Fujifilm (Tallahassee, FL)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... enterprise quotes. + Understand the specialized requirements for quoting regulated medical software, hardware, and consulting; ensuring accurate compliance ,… more
    Fujifilm (10/29/25)
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  • Regulatory Affairs Manager

    Dentsply Sirona (Sarasota, FL)
    …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... partners for registrations in their respective countries to ensure compliance globally and acts as an internal champion for...13485, EU MDR). + Experience with software as a medical device , AI and/or medical more
    Dentsply Sirona (09/18/25)
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