Join a dynamic regulatory team responsible for managing regulatory matters related to Stepan’s biocide portfolio.
Manage Stepan’s Biocide Formulator Audit Program and associated regulatory agency audits.
Complete audits with internal resources or via third-party audit companies.
Manage the interface with third-party audit companies and prepare materials for formulators.
Participate in label reviews and collectively ensure compliance with EPA FIFRA regulations.
Support Stepan’s Biocide Network and License Approval Process.
Develop and implement compliance programs, conducting audits, managing risk and effectively training personnel.
Requirements
Must have 3
5 years of regulatory experience with a chemical company.
Must have FIFRA registration experience; experience with Antimicrobials is beneficial.
Ability to interact effectively with business leaders, government agencies and trade associations.
Excellent teamwork and interpersonal skills.
Strong competency in project management, negotiation, and communication.
Strong business acumen, problem solving and decision-making skills.
Ability to communicate complex technical regulatory issues with diverse audiences and personnel, including internal stakeholders and regulatory authorities.
Ability to work with cross-functional teams and effectively manage multiple projects, including the creation of project plans and timelines while organizing and tracking complex information.