Human Health Regulatory Affairs Intern

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.

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.

Required Qualifications

• Currently enrolled in an associate bachelors masters 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.

• 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.

• Full-time internship assignment lasting approximately 10 weeks.
• Located on-site at our West Allis WI facility.

Expected salary: $23/hr

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 humanitys biggest challenges. Since we began more than a century ago this has been our guide. Its how weve gotten so far. And its how well 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.

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