• Associate Director, Regulatory Affairs

    United Therapeutics (Austin, TX)
    …daughter's pulmonary arterial hypertension( **PAH)** . Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... ), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans… more
    United Therapeutics (08/10/25)
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  • Principal Vascular Therapy Development Rep…

    Medtronic (Houston, TX)
    …degree + 7+ years B2B or Healthcare Sales with 4+ years experience selling Medical device or medical capital equipment **NICE TO HAVE- DESIRED/PREFERRED ... timely and sound decisions. + Thorough working knowledge of medical terminology, medical procedures and the medical device industry. + Excellent customer… more
    Medtronic (08/23/25)
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  • AFM Scientist

    ARTIDIS (Houston, TX)
    …tissue/cell nanomechanics, sample preparation, and quantitative data analysis. + Familiar with medical device operations, ISO 13485, FDA guidelines, CE ... and optimize measurement protocols, and ensure the highest standards of data quality , reproducibility, and regulatory compliance. You will work closely with research… more
    ARTIDIS (08/16/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Austin, TX)
    …United States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... 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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  • Director, Regulatory Operations

    Stryker (Flower Mound, TX)
    …regulatory requirements, including ISO, FDA , and International requirements (ie, Medical Device Regulation) + Demonstrated expertise in regulatory systems in ... May serve as Person Responsible for Regulatory Compliance (PRRC) under the EU Medical Device Regulation + May take responsibility for handling regulatory agency… more
    Stryker (08/22/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Austin, TX)
    …and II + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...Provides on-going support to resolve application related and image quality concerns on both a product and system level.… more
    Fujifilm (08/11/25)
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  • Senior Technical Clinical Consultant (PACS,…

    Fujifilm (Austin, TX)
    …management. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
    Fujifilm (06/19/25)
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  • Staff Software Engineer

    Abbott (Irving, TX)
    …reviews, andquality assurancepractices. **Preferred Qualifications:** + Experience in themedical device industryor other regulated environments (eg, FDA , ISO ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (07/26/25)
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  • Research Coordinator - Surgery

    Houston Methodist (Houston, TX)
    …as per protocol including participant records, drug documentation, reconciling study drug/ device accountability; monitors documentation for quality and accuracy. ... proper procedures to research coordinator and research coordinator assistant. ** QUALITY /SAFETY ESSENTIAL FUNCTIONS** + Oversees and maintains accurate source… more
    Houston Methodist (08/13/25)
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  • Lead Project Engineer

    Fujifilm (Austin, TX)
    …or processes. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical...with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical… more
    Fujifilm (08/13/25)
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