Become a Leader in Public Health: Deputy Office Director at the FDA
The Food and Drug Administration (FDA) is the cornerstone of consumer protection and public health in the United States. If you are a high-level legal or regulatory professional with a passion for public service, the Center for Drug Evaluation and Research (CDER) offers a unique opportunity to shape the future of medical product safety. We are currently seeking a Deputy Office Director (Supervisory Regulatory Counsel) to join our team in Silver Spring, Maryland.
Job Responsibilities
As a Deputy Office Director, your primary duties will include:
- Policy Oversight: Supporting the ODSIR Director in managing drug import, export, and recall programs.
- Supply Chain Integrity: Implementing standards under the Drug Supply Chain Security Act (DSCSA).
- Incident Response: Leading the response to urgent public health crises, including drug shortages and counterfeit threats.
- Leadership & Representation: Serving as a primary representative in meetings with state and federal agencies and industry leaders.
Requirements
To qualify, applicants must meet specific professional and educational benchmarks:
| Requirement Type | Specification |
|---|---|
| Education | J.D. or LL.M. from an accredited institution |
| Experience (w/ Degree) | 4 years of relevant regulatory experience |
| Experience (w/o Degree) | 11 years of relevant regulatory experience |
| Citizenship | Must be a U.S. citizen |
Salary Overview
This position is filled under the Title 21 streamlined hiring authority, which provides a competitive salary structure. The current range is $194,932 to $308,053 per year, commensurate with experience and qualifications.
Benefits
- Federal health, dental, and vision insurance.
- Participation in the Federal Employees Retirement System.
- Generous annual leave and sick leave accrual.
- Potential for student loan repayment and relocation incentives.
Application Tips
Submit a comprehensive two-page resume that details your accomplishments, duties, and salary history. Ensure all transcripts are included, and pay close attention to formatting—secured PDFs may cause system errors. Most importantly, ensure your questionnaire responses are original.
This role is more than a job; it is a commitment to the safety of our nation. If you meet the criteria and are ready to tackle complex regulatory challenges, we encourage you to apply by the July 24, 2026, deadline.
Why This Deputy Office Director (Supervisory Regulatory Counsel) Job Matters
Shape the future of public health and drug safety at the FDA as a Deputy Office Director. Lead critical compliance initiatives at the intersection of law, policy, and medicine.
Deputy Office Director (Supervisory Regulatory Counsel) Job Overview
The Food and Drug Administration (FDA) is seeking a visionary Deputy Office Director (Supervisory Regulatory Counsel) to join the Center for Drug Evaluation and Research (CDER). Based in Silver Spring, Maryland, this high-impact role oversees the integrity of the U.S. drug supply chain, managing complex regulatory enforcement, import/export policies, and emergency response to public health threats. You will play a pivotal role in shielding patients from substandard or counterfeit drug products while collaborating with senior federal and state leadership.
Requirements for Deputy Office Director (Supervisory Regulatory Counsel)
- Possess a Juris Doctor (J.D.) or Master of Laws (LL.M.) degree from an accredited institution.
- Demonstrate at least 11 years of comparable regulatory experience in interpreting laws, regulations, or policies.
- Must meet one of the following experience thresholds: A law degree combined with 4 years of regulatory experience, OR 11 years of specialized regulatory experience.
- Submit official or unofficial transcripts demonstrating education requirements.
- Must be a U.S. citizen.
- Ability to obtain and maintain a High-Risk security clearance.
Preferred Qualifications for Deputy Office Director (Supervisory Regulatory Counsel)
- Proven track record in policy development related to drug supply chain security.
- Strong expertise in the Federal Food, Drug, and Cosmetic Act.
- Experience in cross-agency collaboration and coordinating with federal law enforcement or regulatory partners.
- Demonstrated ability to lead during urgent public health crises or drug shortage scenarios.
Federal Benefits & Perks
- âś“Comprehensive federal health insurance and retirement plans (FERS).
- âś“Generous paid vacation and sick leave.
- âś“Access to professional development and leadership training programs.
- âś“Flexible work environments, including potential telework eligibility.
- âś“Relocation or recruitment incentives may be available for qualified candidates.
đź’ˇ How to Apply Deputy Office Director (Supervisory Regulatory Counsel) Job & Insider Tips
Application Steps for Deputy Office Director (Supervisory Regulatory Counsel) Job
- Ensure you have a registered account at Login.gov.
- Prepare a detailed, two-page resume that outlines your complete employment history, salary, and duties.
- Collect all relevant academic transcripts and professional licensure documents.
- Complete the online questionnaire via the FDA application portal.
- Submit your application package before the closing date of July 24, 2026.
đź’ˇ General Tips
- Ensure your resume includes specific dates, hours worked, and salary for every role listed.
- Double-check that all digital files are in non-secured formats so they are readable by the system.
- Be prepared for potential follow-up requests, including writing samples or references.
- Utilize the FDA Applicant Help Desk if you encounter technical difficulties.
- Avoid using AI tools for your application questionnaire; the FDA requires certification of original work.
Frequently Asked Questions
Is a law degree strictly required for this position?
Not necessarily. You may qualify if you possess 11 years of directly comparable regulatory experience in law and policy interpretation, even without a J.D. or LL.M.
What is the pay scale for this position?
This position is hired under Title 21 Pay Table 2, Band F, with a salary range of $194,932 to $308,053 per year.
Job from Food And Drug Administration
The FDA is responsible for protecting public health by ensuring the safety, efficacy, and security of human and veterinary drugs, medical devices, and the nation’s food supply. Working within the Office of Compliance, you will contribute to a legacy of science-based regulation and enforcement that impacts the daily lives of millions of Americans.