Get more replies from employers
Send a job-specific resume in minutes.
U.S. Food and Drug Administration (FDA)
FDA-CDER-2026-0101
9/30/2026 3:00:00 PM Eastern Time Zone
All documents must be in English or include an official English translation.
Applications will be reviewed on a rolling basis.
Center for Drug Evaluation and Research (CDER), Office of Pharmaceutical Quality (OPQ), Office of Pharmaceutical Quality Research (OPQR), Silver Spring, Maryland.
As a postdoctoral fellow, you will join a project to research the glycan release from glycoprotein drugs with chemo-enzymatic methods and characterize glycan structures with state‑of‑the‑art technologies, including high‑performance liquid chromatography (H(U)PLC) and mass spectrometry (MS).
Under the guidance of the mentor, you will learn and develop technologies for feasible analysis of glycosylation of therapeutic glycoprotein drugs, including monoclonal antibody drugs, fusion proteins, enzyme‑replacement therapies, plasma products, etc., in manufacturing control and characterization.
Tongzhong Ju (Tongzhong.Ju@fda.hhs.gov)
This opportunity is available to U.S. citizens, lawful permanent residents (LPR), and foreign nationals with valid immigration statuses that are acceptable for program participation.
Participants do not become employees of FDA, DOE, or the program administrator, and there are no employment‑related benefits.
ORISE Fellows, including spouse and minor children, must report any significantly regulated organization (SRO) relationship or prohibited investment fund financial interest. Failure to divest or terminate the relationship results in ineligibility for FDA placement. For additional requirements, see FDA Ethics for Nonemployee Scientists.
The qualified candidate should have received a doctoral degree in a relevant field, or be currently pursuing a doctoral degree with completion before September 29, 2026. The degree must have been received within five years of the appointment start date.
Ashley