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Laboratory Director

Employer
US FDA Office of Regulatory Affairs
Location
Jefferson, Arkansas
Salary
Starting at $177,123
Closing date
May 27, 2023

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Field of specialization
Analytical, Biochemical, Biological, Food, Microbiological
Work Function
Management-Laboratory
Job Type
Full time

Job Details

The Arkansas Human & Animal Food Laboratory (ARLHAF) serves the ORS, the ORA and its field organization based on ORA’s scientific program needs and capabilities. The laboratory conducts laboratory testing and analysis of samples to assess their compliance with applicable laws and regulations enforced by the FDA and to determine the extent to which findings provide evidence of violative conditions and practices.
Duties/Responsibilities:
• The Laboratory Director manages all phases of the multi-disciplinary Human and Animal Food laboratory programs and analyses aimed at effective accomplishment of the Agency’s consumer protection mission. The Laboratory Director is responsible for planning, organizing, staffing, directing, controlling, and budgeting of resources and operations to attain maximum accomplishment of the ORS, ORA, and FDA Human and Animal Food programmatic objectives.
• Participates fully in formal and informal policy and planning activities to formulate the overall program operating goals, objectives, and milestones for the ARLHAF in support of Southwest region and the FDA. Reviews short and long-range operations, workplans and programs, as well as makes substantive recommendations on changes that will improve laboratory services and the quality of customer services.

Develops, approves, and modifies operating procedures and practices within the ARLHAF, ensuring the most effective application, while recommending required revisions of multi-regional and nationwide operating procedures and policies aimed at enhancing the quality of customer service so that work products are fit for the intended use of the customers and stakeholders.
• Ensures that program evaluation review techniques, quality assurance and quality management systems, strategies, measures, and economical operating practices are in place to promote the effective execution of work plans, conformance to policy and safe working practices.
• Programmatic responsibilities include analysis of regulatory samples, development of analytical methods, providing scientists for consumer protection mission, including determining compliance of regulated products and enterprises with the Federal Food, Drug, and Cosmetic Act, related regulations, and legislation, and advancing FDA science.

Company

Introduction
The Food and Drug Administration (FDA) is the regulatory, scientific, public health, and consumer protection agency responsible for ensuring that all human and animal drugs, and medical devices are safe and effective, that cosmetics, foods, food additives, drugs and medicated feeds for food producing animals, and radiation emitting devices are safe, and that all such products marketed in the United
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States are adequately, truthfully and informatively labeled and safely and properly stored, transported, manufactured, packaged and regulated. FDA’s programs are national in scope and effect, and the agency’s activities have a direct and significant impact on multi-billion-dollar industries, in addition to protecting the health and safety of American Consumers. The work of the Agency is carried out by a staff of more than 18,000 scientists, physicians, regulatory and other personnel stationed throughout the United States and abroad.
The Office of Regulatory Affairs (ORA) is at the forefront of building a public health safety net for today’s complex, global regulatory environment. ORA professionals work in a range of program areas and locations, with 227 offices and 13 laboratories throughout the United States. As the lead office for all FDA field activities, ORA serves as the agency’s direct connection with regulated industry through a) inspections of firms and plants producing FDA-regulated products, b) investigations of consumer complaints, emergencies and criminal activity, c) enforcement of FDA regulations, d) sample collection and analysis, and e) review of imported products.
To view our ORA Vision, Mission, and Values please visit: https://www.fda.gov/about-fda/office-regulatory-affairs/ora-vision-mission-and-values.

Company info
Website
Telephone
240-402-1049
Location
12420 Parklawn Drive
Room 2113
Rockville
MD
20852
US

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