Rebecca Mannion Email & Phone Number

Monitoring regulatory changes and inspection trends • Client research and data compilation • Antimicrobial market trends and direction • Managing GLP contract laboratory product chemistry and toxicity studies • Utilize NPIRS and EPA databases for competitive surveillance • EPA submission strategy • Audit manufacturing sites for GMP and EPA Books and Records compliance

Sturtevant, Wi

Provided analysis, advice, expertise and project management for North American registrations (EPA FIFRA; FDA Cosmetic, Drug and Medical Device; and Health Canada NNHPD and Bureau of Chemical Safety) and third-party certifications (Kosher, Halal). I negotiated with government agencies on projects, as well as areas of policy as needed, to obtain approvals of new products and amendments with business objectives in mind.I participated in industry trade associations to keep current with changing regulations and guidance, as well as provided input to advance business viewpoint.I submitted and maintained registrations for 30+ antimicrobial and biocidal productsI provided strategic direction to the Registered Products staff to ensure that activities and programs met all applicable regulatory requirements as well as supported the business.I supported to local countries for international registration of North American products. I acted as the registration advisor and Quality Assurance Unit (QAU) manager to the Good Laboratory Practices (GLP) program.

Sturtevant, Wi

Submitted applications and amendments to the US EPA to obtain and maintain registrations. Advised product managers and business partners on registration issues. Managed commercialization projects. I obtained approvals or negotiated next steps for amended products.I assisted with export and import of antimicrobial products without any warnings/citations.I acted as the registration advisor and QAU manager to the GLP program.

Sturtevant, Wi

Updated EPA registered product labels per Federal and state guidelines, as well as those of basic registrants, to obtain approvals. Submitted applications and amendments to the state of California Department of Pesticide Regulation. Tracked registration activities of the department and maintained filing system.I updated export labels and provided information for import. I provided registration documents for global export of NA Registered Products. I acted as QAU Administrator and Auditor in the GLP program ensuring quality data developed to support antimicrobial products, with no violations, findings, or issues.I coordinated with formulators to obtain supplemental registrations and easily gained state registration.

Sturtevant, Wi

Registered new pesticide products and renewed licenses of existing products in the US. Tracked the registration status and fees required/paid. Maintained state/sales shipping restrictions in business operating systems. Submitted notifications and amendments to states as changes occurred to existing products. I completed renewals on time with no fines or late fees, and projected budgets accurately.I reviewed EPA registered product labels for compliance and state approval.

Racine, Wi

Contractor - S.C. Johnson Wax, Product Toxicology Wrote adverse effects summaries from product placement studies for the toxicologists and governmental reporting purposes. Maintained spreadsheet of results of air care product placement studies for department database.Contractor - JohnsonDiversey, Inc., North America Regulatory & ComplianceTracked raw materials, requested evaluation forms and reviewed for compliance. Built data entries in business management system for raw materials with regulatory information and formulas.Administrative Assistant/Bookkeeper – Leifheit & Co.Handled bookkeeping including calculating payroll, balancing cash disbursements, and calculating reimbursements of expenses and other clerical duties.