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This position is located in the Department of Health and Human Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Denver District Office located in Denver, CO.
The FDA's Office of Regulatory Affairs is the lead office for all FDA Field activities as well as providing FDA leadership on imports, inspections, and enforcement policy. ORA supports FDA Product Centers by inspecting regulated products and manufacturers, conducting sample analysis on regulated products, and reviewing imported products offered for entry into the United States. ORA also develops FDA-wide policy on compliance.
Who May Apply: Open to all United States Citizens.
This announcement may be used to fill additional vacancies.
The incumbent will perform the full range of analytical chemistry procedures, including radiochemistry procedures, on a variety of samples, including the difficult, complex or unusual samples submitted by agency personnel in connection with regulatory monitoring and enforcement activities. Duties could also include research and development of analytical methods.
Before analyzing a sample, reviews the background material submitted with the sample, agency reports on similar samples or situations and pertinent regulations.
Determines the approach, methods, and procedures to use to obtain the information requested, taking into consideration the requirements established by Agency regulations and Federal law.
Writes a report that identifies the sample, shows the methods and procedures used, any modifications data, the results and their interpretation, and whether the sample appears to be in violation of any agency regulation.