• Help



    The position is located in the United States (U.S). Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Office of Regulatory Science (ORS). ORA's mission is to protect consumers and enhance public health by maximizing compliance of FDA regulated products and minimizing risk associated with those products. ORA is responsible for inspecting products and manufacturers, conducting sample analyses of regulated products, and reviewing imported products offered for entry.

    Learn more about this agency


    • Writes reports stating the results and conclusions documenting the nature of any regulatory violation.
    • Skill in oral and written communication to prepare and present analyses; provide guidance; solicit information; draft position papers; defend proposals; and prepare materials to support work.
    • Analyzes difficult, novel and complex samples.
    • Reviews background materials, agency reports and pertinent regulations.
    • Has knowledge of chemistry theories, practices, and established methodology sufficient to analyze complex and unprecedented samples and as needed to develop and modify analytical methods.
    • Holds responsibility for quality control and quality assurance data.
    • As assigned, accompanies Agency personnel on inspections and acts as a technical advisor.
    • Responsible for assuring that the analysis and methods development work maintains the environmental integrity of the work site and products analyzed.

    Travel Required

    25% or less - You may be expected to travel for this position.

    Supervisory status


    Promotion Potential


  • Job family (Series)

    1320 Chemistry

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/613797900. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.