2026 Regulatory Affairs Co-op (6 Months, July 2026 Start)

Haleon

Warren, NJ, USA
Hourly: $24.50; bonus/equity: not specified; benef...
Start date july 1, 2026
Full-time 40 hours per week
On-site work in new jersey
This role offers an opportunity to support process improvements and ensure compliance within the Regulatory Affairs team at a world-leading consumer healthcare company

Job Summary

  • This role offers an opportunity to support process improvements and ensure compliance within the Regulatory Affairs team at a world-leading consumer healthcare company.
  • The incumbent will be responsible for maintaining accurate product registrations, managing document metadata, and categorizing FDA correspondences in the electronic data management system.
  • Candidates will gain visibility into FDA submission documentation, including New Drug Applications (NDAs) and Investigational New Drugs (INDs), while contributing to identifying emerging regulatory trends.

Matching Summary

This role offers an opportunity to support process improvements and ensure compliance within the Regulatory Affairs team at a world-leading consumer healthcare company.

Salary

Hourly: $24.50; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Start date July 1, 2026
  • Full-time 40 hours per week
  • On-site work in New Jersey
  • US work authorization required

Nice-to-have

  • Experience with Microsoft Word and Excel
  • Prior experience with eDMS systems
  • Strong analytical and organizational skills
  • Ability to present insights to teams

Key Requirements

  • Enrolled in bachelor's degree program
  • Graduating between December 2026 and May 2028
  • Major in Science, Biology, Pharmacy, or related field
  • Minimum cumulative GPA of 3.0 preferred
  • Must not require future visa sponsorship

Work Rights

Must be eligible to work in the US

Tailored Resume

Cover Letter