Regulatory Affairs Specialist

Date Posted: 11/04/2025 Hiring Organization: Rose International Position Number: 490953 Industry: Biotech/Healthcare Job Title: Regulatory Affairs Specialist Job Location: Chesterfield, MO, USA, 63017 Work Model: Hybrid Work Model Details: 3 days a week onsite Shift: M-F first shift Employment Type: Temporary FT/PT: Full-Time Estimated Duration (In months): 6 Min Hourly Rate ($): 35.00 Max Hourly Rate ($): 40.00 Must Have Skills/Attributes: Regulatory, Regulatory Affairs, Regulatory Compliance Experience Desired: Experience with document comparison tools (2 yrs) Required Minimum Education: Bachelor’s Degree C2C is not available Job Description Drug screen & criminal background check will be required EDUCATION / EXPERIENCE REQUIREMENTS • BA/BS in a field of science, business, or a related degree plus 2 years of professional working experience. REQUIRED SKILLS • Strong attention to detail. • Highly developed written and oral communication skills. • Proficiency in Microsoft Office suite. • Database management experience. • Strong problem-solving skills. • Ability to multitask and manage multiple projects effectively. • Ability to work independently as well as collaboratively within a team environment. • Experience with document comparison tools is a plus. POSITION SUMMARY We are seeking a dedicated and detail-oriented individual to join our team for a six-month role with the potential for extension based on performance. In this position, you will play a crucial role in managing state regulatory activities related to crop protection products. Your responsibilities will include communicating with regulatory agencies, maintaining databases, processing registration fees, and ensuring compliance with federal and state requirements. This is an excellent opportunity for someone looking to contribute to a dynamic team while gaining valuable experience in regulatory affairs. RESPONSIBILITIES • Support the team in managing state regulatory activities necessary for obtaining and maintaining registrations including FIFRA Sections 3, 24(c), 2(ee), 18, and 5 for crop protection products. • Communicate with state regulatory agencies regarding submissions, approvals, renewals, and other related matters. • Maintain and update regulatory databases and internal tracking systems. • Scan regulatory mail and supporting documents, filing them electronically. • Track and process payment of state registration fees, including new product registration fees and annual renewal fees. • Review product labels for accuracy and consistency. • Ensure 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 documents, file them in databases, or mail them to designated recipients. • Perform other assignments as required. Only those lawfully authorized to work in the designated country associated with the position will be considered. Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements. Benefits: For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay Equity: For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Location: Chesterfield, Missouri, US

Posted Date: 11/17/2025