The U.S. Food and Drug Administration (FDA) is seeking five experts on medical device manufacturing practices to participate in FDA’s Device Good Manufacturing Practice Advisory Committee (DGMPAC) next year. This position would be the public expert advocate on this committee.
The DGMPAC reviews proposed regulations for good manufacturing practices governing the methods used in, and the facilities and controls used for, the manufacture, packing, storage, and installation of devices, and makes recommendations on the feasibility and reasonableness of the proposed regulations. Learn more on the FDA website.
Applicants will be required to submit their CV and go through a conflict of interest process. For more information, please contact Jarrod Collier Jarrod.Collier@fda.hhs.gov by December 3, 2021.