Americas Regulatory Affairs Intern

VylorVylorDes Moines, Iowa, United States
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Posted

9/11/2026

Employment

Intern

Range

Check website

Work style

Hybrid

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AI summary

Core responsibilities

The intern will support regulatory activities, including biotechnology product registrations, dossier preparation, and compliance in North America. They will also gather market intelligence, update product documentation, and collaborate with cross-functional teams on regulatory advocacy initiatives.

Requirements overview

Candidates must be currently enrolled in an accredited college or university with a minimum cumulative GPA of 3.0, preferably in a biological field. Strong attention to detail, effective data management skills, and the ability to work collaboratively are essential for this role.

Key skills

Regulatory affairsBiotechnologyData managementMarket intelligenceRegulatory submissionsComplianceDossier preparationDocument organizationRegulatory database managementProduct labelingSafety data sheetsRegulatory advocacyCommunication skillsLearning agilityAttention to detailCollaboration

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Education requirements

postgraduate degree

About Vylor

Industry

Biotechnology Research

Employees

138

Type

Public Company

Size

10,001+ employees

Vylor is an advanced seed and genetics company emerging from a planned separation from Corteva Agriscience in Q4 2026. Anchored in elite germplasm and cutting‑edge biotechnology, Vylor leverages next‑generation science, such as gene editing and molecular breeding, to strengthen its core business and expand into new opportunities. The company will scale innovation through leading routes to market and a growing global licensing platform.

Job categories

AgricultureScience & ResearchLegal

Description

Join Vylor—Powering the Future of Agriculture​ At Vylor, we’re advancing agriculture through breakthrough science—combining elite germplasm, cutting-edge biotech, and next-generation expertise in gene editing and molecular breeding. Our portfolio includes trusted industry brands like Pioneer®, Brevant®, and Hoegemeyer®, delivering performance farmers rely on.​ Join us to help scale innovation globally and shape what’s next in crop science. We have an exciting opportunity for a Regulatory Affairs Intern to join our team at our Johnston, IA location. In this role, you will support regulatory activities related to biotechnology product registrations and compliance in North America. You will gain hands-on experience working with regulatory submissions, data management, market intelligence, and regulatory advocacy while collaborating with cross-functional teams. What You’ll Do: Support North America regulatory submissions, including 4th Generation Corn Lep trait and soybean stack submissions. Assist with regulatory administration, dossier preparation, document organization, and regulatory database updates. Gather market intelligence data and analyze public comments related to newly published biotech events. Review and update product labels, Customer Safety Forms (CSFs), and Safety Data Sheets (SDSs). Support regulatory advocacy initiatives and other regulatory affairs projects as assigned. What Skills You Need: Minimum cumulative GPA of 3.0. Current enrollment at an accredited college or university; post-graduate preferable related, but not limited, to a biological degree Strong attention to detail and ability to manage and organize data effectively. Ability to work collaboratively with a variety of stakeholders and cross-functional teams. Strong learning agility, initiative, and willingness to take on new challenges. Excellent written and verbal communication skills. Are you a good match? Apply today! We seek applicants from all backgrounds to ensure we get the best, most creative talent on our team. Corteva announced to separate our current advanced seed and genetics business to establish a standalone company, operating as Vylor, Inc. The process of the planned separation is anticipated to be completed the fourth quarter of 2026, subject to legal requirements and board approval. Should you accept this position, it is anticipated that, following conclusion of the separation, you would be an employee of Vylor, Inc. and your employment would be governed by Vylor, Inc. employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by Vylor, Inc. at an appropriate time and subject to any necessary consultation processes. Vylor is an equal opportunity employer. We are committed to embracing our differences to enrich lives, advance innovation, and boost company performance. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, military or veteran status, pregnancy related conditions (including pregnancy, childbirth, or related medical conditions), disability or any other protected status in accordance with federal, state, or local laws.

Requirements

  • Regulatory affairs
  • Biotechnology
  • Data management
  • Market intelligence
  • Regulatory submissions
  • Compliance
  • Dossier preparation
  • Document organization
  • Regulatory database management
  • Product labeling
  • Safety data sheets
  • Regulatory advocacy
  • Communication skills
  • Learning agility
  • Attention to detail
  • Collaboration

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