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

Haleon

Warren, NJ, USA
Hourly: $24.50; bonus/equity: not specified; benef...
Fda submission documentation knowledge
Electronic data management system maintenance
Microsoft excel and word proficiency
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 co-op associate will be responsible for tracking and categorizing FDA eCTDs, managing registration metadata, and analyzing historical submission data to identify emerging trends.
  • Candidates will gain visibility into FDA submission structures, including Investigational New Drugs and New Drug Applications, while working on-site in Warren or Berkeley Heights, NJ.

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

  • FDA submission documentation knowledge
  • Electronic Data Management System maintenance
  • Microsoft Excel and Word proficiency
  • Full-time availability Monday-Friday
  • Accurate metadata management skills

Nice-to-have

  • Experience with eDMS systems
  • Ability to present insights to teams
  • Interest in regulatory compliance trends
  • Strong organizational and analytical skills

Key Requirements

  • Enrolled in Science, Biology, Pharmacy degree program
  • Graduation between December 2026 and May 2028
  • Eligible to work in the US without future sponsorship
  • Must start July 1, 2026
  • Cumulative GPA of 3.0 preferred

Work Rights

Must be eligible to work in the US

Tailored Resume

Cover Letter