Regulatory Affairs Specialist, North America

Ridley International Ltd•Mankato, MN

72d

About The Position

The North America Regulatory Specialist is responsible for supporting regulatory compliance and product registration activities throughout North America. This position ensures that Alltech s products, facilities, and documentation meet applicable federal and state regulatory requirements for animal feed and pesticide products. The Specialist works cross-functionally with internal departments and external regulatory agencies to maintain Alltech s strong compliance standing and support ongoing market access across the region.

Requirements

Strong knowledge of North American regulatory frameworks and standards related to animal feed and pesticide products
Excellent written and verbal communication skills
High attention to detail and commitment to accuracy
Ability to effectively interact with all levels of employees and customers
Analytical and critical thinking skills
Talent to manage multiple projects and deadlines
Proficient in Microsoft Office and relevant software
Strong work ethic with the ability to multitask
Excellent organizational skills and ability to maintain confidentiality
Bachelor s degree in Animal Science or related field (or equivalent industry experience). Master s degree preferred.
5+ years experience in animal science or nutrition, quality assurance or regulatory compliance within an animal food manufacturing environment.

Nice To Haves

Fluency in a foreign language would be an asset.

Responsibilities

Support the preparation and submission of new product registration applications across North America
Provide technical support to answer scientific related questions from regulators, customers and sales.
Provide support for facility licensing requirements throughout North America
Maintain existing product and facility registrations to ensure continued compliance
Conduct regulatory research and review applicable federal and state laws and regulations
Maintain cooperative working relationships with internal teams, external partners, and regulatory authorities.
Provide technical review of product documentation and labeling
Assist in preparing and executing regulatory registration strategies and plans
Track and manage regulatory projects and deadlines to ensure timely submissions and renewals.
Organize and verify product development information to ensure regulatory compliance of ingredients, formulations, and labels
Assist in resolving regulatory challenges and responding to inquiries from regulatory agencies and customers.
Maintain accurate and organized records related to international regulatory activities
Attend various training programs to obtain and maintain expertise in applicable issues