What are the responsibilities and job description for the Regulatory Affairs Specialist (Mid) position at Planet Pharma?
Job Description
Target Pay Rate: 38-43.49/hr **salary will be commensurate with experience?
Tasks And Responsibilities
Target Pay Rate: 38-43.49/hr **salary will be commensurate with experience?
Tasks And Responsibilities
- Manage the state regulatory activities necessary to obtain and maintain registrations including, FIFRA Sections 3, 24(c), 2(ee), 18, 5 for crop protection products;
- Compile and submit required data and documents necessary for registration across all States.
- Manage and submit monthly, biennial and annual renewals for assigned products.
- Communicate with State regulatory agencies regarding submissions, approvals, renewals and etc.
- Maintain, update and extract data from regulatory databases.
- Review product labels for accuracy and consistency.
- Track and Process payment of state registration fees, including but not limited to, new product registration fees, annual state renewal fees, tonnage and etc.
- 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.
- BA/BS in a field of science, business, or a related degree plus 4 years of regulatory experience
- Experience interpreting and complying with laws & regulations to support regulatory submissions/approvals.
- Strong attention to detail is required.
- Highly developed written and oral communication skills.
- Advanced knowledge of the Microsoft Office suite.
- Experience successfully managing information in databases.
- Ability to multitask and manage multiple projects in a fast-paced environment.
- Ability to work both independently and in a team environment.
- Experience with document comparison tools is a plus.
