Zimmerman Associates, Inc. (ZAI) is seeking a Lead Regulatory Data Specialist to support the Center for Tobacco Products (CTP), Office of Compliance and Enforcement (OCE), at the U.S. Food and Drug Administration (FDA). This role is responsible for leading and managing a team of regulatory data specialists while supporting data preparation, workflow development, and documentation in accordance with regulatory standards.

Duties / Functional Responsibilities:

• Leads, supervises, and manages a team of regulatory data specialists
• Creates workflows that map to regulatory standards
• Prepares data for output to a variety of printed and electronic media
• Maintains accurate and up-to-date documentation of project status
• Works closely with the project/task manager to ensure and document standard operating procedures (SOPs) that support data quality and production efficiency

Required Qualifications:

• None specified

Preferred Qualifications

• Minimum of four (4) years of experience
• Bachelor’s degree

Zimmerman Associates, Inc. is an Equal Opportunity Employer. In accordance with federal and state laws, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, veteran status, or any other legally protected status.