• Principal Vascular Therapy Development Rep…

    Medtronic (Austin, TX)
    …degree + 7+ years B2B or Healthcare Sales with 4+ years experience selling Medical device or medical capital equipment **NICE TO HAVE- DESIRED/PREFERRED ... to company policies and procedures + Adheres to financial, regulatory , quality compliance standards and requirements. **Influence...+ Thorough working knowledge of medical terminology, medical procedures and the medical device more
    Medtronic (08/08/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Austin, TX)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/11/25)
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  • Senior Clinical Consultant II, International

    Fujifilm (Austin, TX)
    …I. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The resource will assist with the development...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
    Fujifilm (08/08/25)
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  • Research Coordinator II

    Houston Methodist (Houston, TX)
    …to gain access to an investigational medical product (drug, biologic, or medical device ) for treatment outside of clinical trials when no comparable or ... methods specified in the study protocol and performing general administrative and regulatory duties supporting the study. This position will also support the… more
    Houston Methodist (07/22/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Austin, TX)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
    Fujifilm (07/24/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Austin, TX)
    …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... program Awareness of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute the shopfloor transaction… more
    Cognizant (07/18/25)
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  • Research Program Project Manager

    Houston Methodist (Houston, TX)
    …ESSENTIAL FUNCTIONS** + Coordinates with CMP staff for the emerging GLP device studies. + Assists in the preparation and coordination of business development ... of the department's major projects/grants. Assists in writing SOP's and other regulatory requirement documentation. + Maintains and provides in-services for the HM… more
    Houston Methodist (08/11/25)
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  • CT Technologist Full Time w/Rotating Call…

    Community Health Systems (Longview, TX)
    …(CT) imaging procedures to assist in the diagnosis and treatment of medical conditions. This role ensures high- quality cross-sectional images for radiologist ... shielding and proper scanning techniques to ensure compliance with regulatory standards. + Performs quality control checks...information in the radiology information system (RIS) and electronic medical record (EMR). + Uses the I-Stat device more
    Community Health Systems (06/20/25)
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  • Technician 1

    Abbott (Plano, TX)
    …and predictable attendance. **Preferred Qualifications** + Technical Diploma. + Prior medical device component inspection experience. + ASQ CMI certification. ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (07/24/25)
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  • Lead Project Engineer

    Fujifilm (Austin, TX)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... consistently high level of customer satisfaction. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that… more
    Fujifilm (08/13/25)
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