Job Overview


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 position is located in the Department of Health and Human Services, Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of Device Evaluation (ODE), Division of Surgical Devices (DSD) in Silver Spring, Maryland.

This vacancy is also being announced concurrently with vacancy announcement HHS-FDA-MP-13-897570 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.

Who May Apply:  Open to all United States Citizens.

This position has supervisory/managerial responsibilities. A one-year supervisory/managerial probationary period is required upon selection/placement.  This may be waived if you have successfully completed the supervisory/managerial probationary period.

This position is also advertised concurrently with HHS-FDA-DE-13-901325, Supv. Interdisciplinary Scientist, HHS-FDA-DE-13-895669, Supv. Interdisciplinary Engineer.  NOTE:  You must apply separately for each announcement in order to be considered.

In addition to base pay, Title 38 Physician/Dentist (PDP) will also be paid.

This announcement may be used to fill additional vacancies.

Announcement amended to extend the closing date.


If selected for this position, you will:

  • Serve as the Division Director and provide executive leadership in managing and directing a scientific, professional, and technical support staff of approximately 50 people;
  • Coordinate the work of subordinate staff and other office personnel involved in the development and execution of general surgery and plastic and reconstructive surgery devices device classification, premarket approval, and research programs;
  • Serve as a top technical expert and advisor and is recognized as a national authority and leader in the medical and reconstructive surgery devices as they relate to investigational device exemptions, premarket notifications, and applications for premarket approval;
  • Develop and coordinate all of the surgical device programs and policies of the Food and Drug Administration;
  • Participate in Inter-Agency task groups as an expert in surgical and reconstructive devices and also participates in technical working groups in other Agencies, such as, the National Institutes of Health;
  • Represent the U.S. Government on issues pertaining to general surgery and plastic and reconstructive surgery devices at meetings with foreign manufacturers, health care professionals and government officials, and at international meetings.