Human Health Regulatory Affairs Intern

Chr. Hansen • West Allis, WI

1d • Onsite

About The Position

Interested in building a career in regulatory affairs while contributing to products that meet the highest standards of compliance and quality? Join the Americas Regulatory Affairs team for a hands-on internship supporting the documentation, coordination, and research that help keep regulated products compliant and market-ready. In this internship, you will contribute to team projects while gaining experience in regulatory operations, content review, compliance monitoring, and data integrity.

Requirements

• Currently enrolled in an associate, bachelor's, master's, or doctoral program in Microbiology, Food Science, Chemistry, Regulatory Affairs, or a related scientific discipline.
• Minimum cumulative GPA of 3.0.
• Relevant coursework or project experience involving food, dietary supplements, ingredients, consumer health products, or another regulated category.
• Proficiency with Microsoft Office; familiarity with workflow or document-management tools is a plus.
• Strong attention to detail, organization, and written communication.
• Ability to interpret scientific or technical information, manage priorities, and collaborate across teams.
• Curiosity, initiative, sound judgment, and commitment to confidentiality and data integrity.

Responsibilities

• Coordinate regulatory requests, projects, deadlines, and supporting information.
• Maintain regulatory systems, databases, records, and document repositories; verify and clean data.
• Draft regulatory documents and organize product, claims, substantiation, and submission files.
• Review marketing, website, and e-commerce content for alignment with approved regulatory language.
• Monitor regulatory and competitor developments and summarize relevant trends and risks.
• Support audit readiness and track workload and project metrics.

Benefits

• Practical experience in a professional Regulatory Affairs environment.
• Exposure to regulatory documentation, compliance monitoring, and audit readiness activities.
• Opportunities to collaborate with experienced regulatory professionals and cross-functional business partners.
• Hands-on learning in claims review, content assessment, project coordination, and regulatory operations.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: Associate degree