Regulatory Affairs Manager, North America

Verdesian Life Sciences; Cary (NC); Hybrid; USD 110,000 - 160,000; Full time

Job summary

Verdesian Life Sciences is seeking a Regulatory Affairs Manager, North America to oversee regulatory activities for its portfolio from the Cary, NC office. You will coordinate product registrations, ensure compliance for crop, animal nutrition, and aquaculture products, and work with Sales, Marketing, R&D, and Business Development to ensure smooth market access worldwide.

The role emphasizes preparing submissions, maintaining regulatory documentation, and interpreting evolving requirements

Qualifications

• Bachelor's degree in Agriculture, Animal Nutrition, Biology, Chemistry, or related field; advanced degree preferred.
• Minimum of 5 years of regulatory affairs experience.
• Strong organizational, analytical, and communication skills.

Responsibilities

• Prepare, review, and submit regulatory filings for assigned projects.
• Support domestic and international product registrations and ongoing compliance.
• Review labels, SDS, specifications and data for regulatory compliance.
• Interpret regulatory changes and communicate business impact.
• Collaborate with agencies, consultants, customers, and regulatory representatives.
• Maintain regulatory records to obtain and sustain product approvals.
• Develop and improve regulatory systems and processes.

Skills

Regulatory affairs

Project management

Communication skills

Analytical

MS Office

Education

Bachelors in life sciences

Advanced degree preferred

Tools

MS Office Suite

Job description

Regulatory Affairs Manager, North America

• Posted : October 20, 2026
• Full-Time
• Hybrid

Locations

Showing 1 location

Cary, NC 27513, USA

Description

Verdesian Life Sciences is seeking an ideal candidate to fill the role of Regulatory Affairs Manager, North America in the corporate office in Cary, North Carolina.

The Regulatory Affairs Manager provides regulatory oversight for Verdesian Life Sciences products, projects, and technologies. This position supports the commercialization of crop, animal nutrition, and aquaculture products through product registrations, regulatory compliance activities, and global regulatory strategy. The role works closely with cross-functional teams, including Sales, Marketing, R&D, and Business Development, to ensure successful market access and compliance worldwide.

• 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 changing regulatory requirements 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 regarding regulatory requirements, labeling standards, export requirements, and compliance concerns.
• Develop and improve regulatory systems, processes, and procedures to support global business growth.
• Maintain regulatory 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 other duties as assigned.

Qualifications

Required

• Bachelor's degree in Agriculture, Animal Nutrition, Biology, Chemistry, or a related scientific discipline; advanced degree preferred.
• Minimum of 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.

Required

• 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.

Verdesian Life Sciences is an equal opportunity employer to all, regardless of age, ancestry, color, disability, military or veteran status, national origin, political affiliation, race, religious creed, sex, and sexual orientation.

Behaviors

Required

Team Player

Works well as a member of a group

Detail Oriented

Capable of carrying out a given task with all details necessary to get the task done well

Leader

Inspires teammates to follow them

Innovative

Consistently introduces new ideas and demonstrates original thinking

Functional Expert

Considered a thought leader on a subject

Motivations

Required

Ability to Make an Impact

Inspired to perform well by the ability to contribute to the success of a project or the organization

Self-Starter

Inspired to perform without outside help

Goal Completion

Inspired to perform well by the completion of tasks

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.