Human Health Regulatory Affairs Intern

Novonesis; West Allis (WI); On-site; USD 28,000 - 36,000; Full time

Job summary

Novonesis in West Allis, WI offers a hands-on Regulatory Affairs internship to support documentation, coordination, and research ensuring product compliance and market readiness. You will gain experience in regulatory operations, content review, and data integrity while contributing to team projects.

The role emphasizes data management, draft regulatory documents, and monitoring regulatory developments, with on-site work for ~10 weeks in West Allis, WI.

Qualifications

• 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.

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.

Skills

Attention to detail

Organization

Written communication

Data interpretation

Cross-team collaboration

Curiosity

Education

Bachelor's in Microbiology/ Food Science/ Chemistry/ Regulatory Affairs

Tools

Microsoft Office

Job description

Interested in a career that matters?Are you 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.The Role & Your ImpactIn this internship, you will contribute to team projects while gaining experience in regulatory operations, content review, compliance monitoring, and data integrity.Key responsibilities include: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.What You’ll Need to Be SuccessfulRequired QualificationsCurrently 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.Essential CompetenciesStrong 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.What We OfferPractical 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.Ways of Working / Working ConditionsFull-time internship assignment lasting approximately 10 weeks.Located on-site at our West Allis, WI facility.CompensationExpected salary: $23/hrRelevant InformationProgram Dates: May 24, 2027 to July 30, 2027Position Type: Temporary position payrolled through a third-party providerApplication Deadline: October 30, 2026Our purpose guides the wayIn Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. If our purpose resonates with you, we encourage you to apply.Opportunities for everyoneWe are committed to an inclusive recruitment process and equal opportunity for all applicants. Therefore we ask you to apply without a cover letter or photo and instead include a few sentences in your CV explaining your motivation for applying.We make all employment decisions based on business needs and welcome candidates with a wide range of backgrounds, including ethnicity, religion, gender, sexual orientation, age, disability, or veteran status.Explore other openingsIf this position isn’t the right fit, you may still find other opportunities with us. You’re welcome to explore open roles or create a job agent to stay connected with future opportunities at novonesis.com/Career