REMOTE – REGULATORY AFFAIRS SPECIALIST (ENTRY)
Planet Pharma · Chesterfield, MO · 2 days ago
On-siteLegalFull-time
Tasks And Responsibilities
- Support the team in the management of state regulatory activities necessary to obtain and maintain registrations including, FIFRA Sections 3, 24(c), 2(ee), 18, 5 for crop protection products.
- Communicate with State regulatory agencies regarding submissions, approvals, renewals and etc.
- Maintain and update regulatory databases and other internal tracking systems.
- Scan regulatory mail and other supporting documents, and file electronically.
- Track and Process payment of state registration fees, including but not limited to, new product registration fees, annual state renewal fees, tonnage and etc.
- Review product labels for accuracy and consistency.
- Maintain compliance by interpreting and evaluating federal and state registration requirements as they apply to our products.
- Provide regulatory support and service to both internal and external stakeholders.
- Respond to inquiries for regulatory information from internal and external stakeholders.
- Scan regulatory and supporting documents, file in databases and/or mail to designated recipients.
- Other assignments, as required.
Requirements
- BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience
- Strong attention to detail is required.
- Highly developed written and oral communication skills
- Proficiency in the Microsoft Office suite
- Database Management experience
- Strong problem-solving skills
- Ability to multitask and manage multiple projects
- Ability to work independently and in a team environment
- Experience with document comparison tools is a plus.