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Summary

Duties

• The duties described are for the full-performance level. At developmental grade levels, assignments will be of more limited scope, performed with less independence and limited complexity.
• The duties may include, but are not limited to:
• Anticipates, develops and implements short and long range regulatory policies for veterinary biologics .
• Develops, reviews, and provides comments on new and revised rules, regulations, and procedures governing the importation, licensure, and testing of veterinary biologics.
• Plans, organizes, and participates in execution of national programs to establish testing standards to assay veterinary biologics prior to release and develop methods to evaluate biological products.
• Cooperates with other staffs and field personnel for the purpose of assuring that the biologics program is being effectively administered.
• Serves as a consultant and advisor to Federal and State officials, various professional and industry organizations, and the general public concerning program objectives.
• Maintains necessary comprehensive and authoritative familiarity with scientific and commercial developments in the field of veterinary medicine, various scientific fields, and vaccine manufacturing.
• Collaborates views of clinical veterinarians, livestock/biologics industries, State-Federal authorities, and domestic and foreign organizations in administration of the Virus-Serum-Toxin Act.
• Reviews current regulations and policies and as well as proposed revisions to ensure they are up-to-date, applicable, and in conformance with the Virus-Serum-Toxin Act.

see official job posting on USAJobs.gov for more information.