Product Stewardship & Reg Analyst

Corteva Agriscience•Indianapolis, IN

16h

About The Position

Corteva Agriscience is seeking a Product Stewardship & Regulatory Analyst (ROS) to join their team. The ROS will be a key member of regulatory teams responsible for assembling and delivering high-quality regulatory documents and submission packages for various submission types for federal and state regulatory submissions for FIFRA and non-FIFRA products. This role requires strong communication skills for interaction with the EPA, state regulatory personnel, and internal departments such as commercial, supply chain, and R&D. The position emphasizes organization, attention to detail, accuracy in data entry, and proofreading to ensure timely and high-quality regulatory actions aligned with registration strategies. The ability to multitask, manage, and adapt to shifting priorities and timelines is crucial as the ROS will manage multiple products. The ROS will also serve as a subject matter expert for internal and external technical capabilities. Key responsibilities include the development, amendment, and maintenance of product labels and labeling in the U.S., coordinating labeling projects with stakeholders, and overseeing the creation and maintenance of Confidential Statements of Formula (CSFs) according to federal guidance. The ROS is responsible for the regulatory submission process, including document preparation and progress tracking.

Requirements

Minimum of an associate degree with at least 5 years of relevant experience in an agricultural chemical industry or other highly regulated industry.
Demonstrated experience in project management within and cross-functional to immediate team to implement complex processes.
Ability to exercise discretion and independent judgment with federal and state regulatory agencies.
The ability to multitask and manage competing priorities are essential due to time sensitive deadlines.
Strong attention to detail and accuracy in proofreading and data entry to produce high quality submission packages.
Strong written and verbal communication skills are required.
High-level of interpersonal effectiveness and teamwork.
Strong computer skills, including proficiency in Microsoft Office are required.
Knowledge of and demonstrated experience with databases and web-based tools.

Nice To Haves

Bachelor’s degree preferred.
Background in agricultural chemical or biological product development or sales, legal, regulatory sciences, or environmental health is useful.

Responsibilities

Work independently and as part of multiple project teams across internal businesses and functions to coordinate and prioritize numerous activities, adapting to shifting priorities and deadlines.
Provide oversight of the entire submission process, from regulatory document creation to submission preparation and execution.
Develop and direct submission processes for label creation and maintenance, addressing regulatory submission feedback, complying with electronic submission processes, and improving internal best practices.
Lead the regulatory process in specific areas of expertise, ensuring consistency, efficiency, and compliance in submission documentation, label creation, CSFs, renewals, payment processing, and tracking/reporting.
Support U.S. Regulatory Team Leaders in assembling documents for regulatory submissions to Federal and State government agencies.
Lead communications and responses with state agencies regarding FIFRA and non-FIFRA submission and reporting requirements.
Resolve state regulatory submission issues and document changes unique to each state.
Oversee direct interactions and correspondence with state officials as needed.
Plan, update, implement, track, and ensure accuracy of regulatory actions and registration strategies in a database.
Respond to communications and actions received from states in functional mailboxes.
Lead the product renewal process at both Federal and State agencies.
Lead or actively participate in regulatory improvement and operational excellence projects.
Create, update, and maintain EPA data matrices.
Validate shipment of products within and to states, ensuring compliance with registration requirements.
Create workflows, dashboards, and reports to facilitate communication of submission status and planning discussions.
Provide internal process leadership and coordination for labels/labeling for a diverse portfolio of products.
Maintain expert knowledge of label-related regulations and policies.

Benefits

Numerous development opportunities offered to build your skills.
Health benefits for you and your family on your first day of employment.
Four weeks of paid time off and two weeks of well-being pay per year, plus paid holidays.
Excellent parental leave which includes a minimum of 16 weeks for mother and father.
Future planning with our competitive retirement savings plan and tuition reimbursement program.

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