Job Overview

Summary

About the Agency

Become a part of the Department that touches the lives of every American! At the Department of Health and Human Services (HHS) you can give back to your community, state, and country by making a difference in the lives of Americans everywhere. It is the principal agency for protecting the health of citizens. Join HHS and help to make our world healthier, safer, and better for all Americans.

This is an Interdisciplinary announcement and may be filled in one of the following series: 0401 (Biologist), 0403 (Microbiologist), or 0415 (Toxicologist).

This position is located at the Department of Health and Human Services (HHS), Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of In Vitro Diagnostics and Radiological Health (OIR), located in Silver Spring, MD.

This vacancy is also being announced concurrently with vacancy announcement FDA-CDRH-MP-17-10012090LH under merit promotion procedures. Please review that announcement to see if you are eligible for consideration under merit promotion procedures. NOTE: Applicants must apply separately for each announcement in order to be considered.

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

Duties

As an Interdisciplinary Scientist in the Office of In Vitro Diagnostics and Radiological Health, you will be responsible for:

  • Acting as a senior reviewer of in vitro diagnostics, medical devices, and/or radiation emitting products in regards to safety and effectiveness;
  • Evaluating medical device submissions in order to report recommendation dispositions to supervisor;
  • Reviewing scientific data related to pre- and post-market notification submissions, radiation emitting products, and/or related supplements and amendments;
  • Enforcing a wide variety of medical devices or radiological health products regulations to provide authoritative guidance to both internal and external groups;
  • Planning and developing audit programs designed to assess conformance with medical regulations or radiological health device standards;
  • Collaborating with other scientists and regulated industry to improve medical device safety or standards for medical devices or radiological health products.

Travel Required

  • Occasional Travel
  • You may be expected to travel domestically for this position up to 5% of the time.

Relocation Authorized

  • No