• Assists in the preparation of International Registration Dossiers and obtaining RUO/Export Only Agreements from foreign countries to market products in Europe, Asia, Latin America and Canada• Responsible for the regulatory review of product labels and literature on company website• Assists in copying, collating, verifying, and compilation of documents required for Field Action Corrections or Removals• Assists in the preparation of documents for third party audits (FDA, State of California, Notified Body) of the Quality Management System• Files training records and document change requests for department• Conducts regulatory research to find current FDA and International Guidances and Regulations in order to compile them for quarterly management review• Participates in internal audits for the company