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    Duties

    Summary

    This position is located in the Department of Health and Human Services (HHS), Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of In Vitro Diagnostics and Radiological Health (OIR) located in Silver Spring, Maryland.

    Additional selections may be made within the same geographical area FDA-wide.

    Learn more about this agency

    Responsibilities

    • Participate in the development and implementation of comprehensive plans and strategies for the internal and external integration of day to day and long-range projects, actions and activities for the assigned organization;
    • Assist in the resolution of complex program or administrative issues or problems. Independently resolves well-precedented issues;
    • Review routine device submissions, supplements and amendments to ensure that they comply with regulation requirements;
    • Give formal or informal training to the staff in implementing revised procedures.
    • Prepare special reports, presentations, and summaries for the Director and Deputy Directors and other office staff.

    Travel Required

    Not required

    Supervisory status

    No

    Promotion Potential

    11

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/511878400. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.