Global Reg Affairs Intern
Johnson & Johnson · Raritan, NJ
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Johnson & Johnson seeks a regulatory affairs intern for a 10-week summer program in their Global Regulatory Affairs division. The role offers hands-on experience in pharmaceutical development, drug labeling, manufacturing controls, and regulatory strategy while working with mentors on real-world projects.
What they're looking for
- Pursuing or earned advanced degree in scientific, technology, or engineering field
- Strong academic track record required
- Legally authorized to work in U.S. without visa sponsorship
- Able to work full-time (40 hours per week) for 10-week internship
- Leadership demonstrated through campus or community activities
- Experience or interest in graphic design, journalism, or creative writing preferred
What you'll be doing
- Work on development programs and strategies for compounds in various stages
- Gain exposure to drug development processes, regulatory laws, and guidance documents
- Apply creative problem-solving to develop insights and business solutions
- Collaborate with other interns on cross-functional projects addressing real challenges
Compensation$23.50-$52.50 per hour based on program year, discipline, degree, and experience
Privacy & handoff
This role links to Johnson & Johnson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.