About the role
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 Impact
In 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 Successful
Required 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.
Essential Competencies
- 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.
What We Offer
- 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.
Ways of Working / Working Conditions
- Full-time internship assignment lasting approximately 10 weeks.
- Located on-site at our West Allis, WI facility.
Compensation
Expected salary: $23/hr
Relevant Information
Program Dates: May 24, 2027 to July 30, 2027
Position Type: Temporary position payrolled through a third-party provider
Application Deadline: October 30, 2026
Our purpose guides the way
In 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 everyone
We 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 openings
If 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 (http://novonesis.com/Career)