C. R. Bard, Inc.

  • Regulatory Affairs Specialist II (MDR)

    Posted Date 10 months ago(2/6/2018 10:47 AM)
    Industry / Category
    Medical Device/ Regulatory Affairs
    Job ID
    Career Level
    Salt Lake City, UT/ Vascular Access Devices - MDS
    US-UT-Salt Lake City
  • Overview

    BARD has now joined BD is a global medical technology company that is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We lead in patient and healthcare worker safety, and technologies that enable medical research and clinical laboratories. Our innovative solutions help advance medical research and genomics, enhance the diagnosis of infectious disease and cancer, improve medication management, promote infection prevention, equip surgical and interventional procedures, optimize respiratory care and support the management of diabetes. 


    Vascular Access Devices, a sub-business unit of Medication Delivery Solutions, focuses on developing, manufacturing, and distributing high-quality medical devices used by clinicians throughout the worldwide healthcare industry to access a patient’s vasculature. Our devices assist in the delivery of chemotherapy, blood products, antibiotics, and nutrition.

    Summary of Position with General Responsibilities

    This position implements C.R. Bard domestic and international regulatory affairs (RA) procedures.  This position may also act as a liaison to Corporate Law Department, providing requested information.

    Essential Job Functions

    The following duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all-inclusive.  The omission of a specific duty or responsibility will not preclude it from the position.

    • Serves as RA representative on project teams.
    • Coordinates the collection of data and information for regulatory submissions; writes the required regulatory submissions for new BAS products.
    • Performs RA reviews for BAS labeling change requests.
    • Coordinate the preparation of International Dossiers with the Product Teams and disseminate the dossiers to the appropriate parties.
    • Travel as required (approximately 5%).

    Basic Qualifications

    • Bachelor’s Degree in Life or Engineering Science, Business, or equivalency.
    • Four (4) years regulatory affairs experience or equivalency, or three (3) years with post-graduate degree.
    • Regulatory experience with premarket notification submissions to FDA and 510(k) compliance.
    • Demonstrated communication and human relation skills.

    The incumbent must demonstrate the potential ability to perform the essential functions of the job as outlined in the duties and responsibilities.

    Additional Desirable Qualifications Skills and Knowledge

    • Understanding of US, CE, and international medical device regulations.
    • High scientific, analytical evaluation skills.
    • Good written and oral communication skills.
    • Ability to work well within cross-functional teams.

    Physical Demands

    This position is in an office environment and requires the incumbent to perform general office functions.

    Work Environment

    The ideal candidate must be able to work in a team oriented, fast paced environment.  Bard Access Systems is an affirmative action, equal opportunity employer that values and actively seeks diversity in the workforce.


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