Regulatory Affairs Manager, North America

Verdesian Brand•Cary, NC

2d•Onsite

About The Position

Verdesian Life Sciences is seeking a Regulatory Affairs Manager, North America, for its corporate office in Cary, North Carolina. The position provides regulatory oversight for company products, projects, and technologies, and supports the commercialization of crop, animal nutrition, and aquaculture products through registrations, compliance activities, and global regulatory strategy. The manager works with Sales, Marketing, R&D, and Business Development to support market access and regulatory compliance worldwide.

Requirements

Bachelor's degree in Agriculture, Animal Nutrition, Biology, Chemistry, or a related scientific discipline.
At least 5 years of regulatory affairs experience.
Strong scientific background and understanding of regulatory processes.
Experience developing and maintaining procedures and documentation.
Strong organizational, analytical, and communication skills.
Ability to manage multiple projects and deadlines simultaneously.
Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.
Experience with regulatory data generation related to product chemistry, toxicology, ecotoxicology, human exposure, environmental fate, or residue chemistry.
Experience working within EPA, PMRA, EU, OECD, or similar regulatory frameworks.
Knowledge of ISO, EU, and OECD standards.

Nice To Haves

Advanced degree.
Bilingual language capabilities.

Responsibilities

Prepare, review, and submit regulatory filings for assigned projects.
Support domestic and international product registrations and ongoing compliance activities.
Review product labels, promotional materials, SDS documents, specifications, and technical data for regulatory compliance.
Interpret and communicate regulatory changes and their business impact.
Collaborate with regulatory agencies, consultants, customers, and international regulatory representatives.
Manage relationships with external regulatory consultants and service providers.
Advise internal teams on regulatory requirements, labeling standards, export requirements, and compliance concerns.
Develop and improve regulatory systems, processes, and procedures to support global business growth.
Maintain records and documentation necessary to obtain and sustain product approvals.
Investigate product complaints and coordinate appropriate regulatory responses when necessary.
Participate in industry associations and regulatory forums on behalf of Verdesian Life Sciences.
Support regulatory projects and perform other duties as assigned.