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    Duties

    Summary

    This vacancy is also being announced concurrently with vacancy announcement FDA-CDER-18-MP-10238623 under merit promotion procedures. Please review that announcement to see if you are eligible for consideration under merit promotion procedures. Applicants must apply separately for each announcement in order to be considered under both options.

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

    Learn more about this agency

    Responsibilities

    • Develop program and projects to identify, assess, and prioritize the public health significance and patient risk associated with drug quality and safety concerns.
    • Plan, develop, and direct strategies and actions that are patient-focused and risk-based to secure the safety, efficacy, and quality of the nation's drug supply.
    • Lead working groups of scientific, regulatory and legal experts within the Center and across the Agency to develop new or revised regulations and draft the resulting rulemaking.
    • Prepare reports and/or written analyses regarding FDA policies and positions on difficult complex matters.

    Travel Required

    Not required

    Supervisory status

    No

    Promotion Potential

    15

This job originated on www.usajobs.gov. For the full announcement and to apply, visit www.usajobs.gov/GetJob/ViewDetails/504413600. Only resumes submitted according to the instructions on the job announcement listed at www.usajobs.gov will be considered.