Regulatory Affairs Internship at Johnson & Johnson USA
Launch your regulatory and life science career with a prestigious Regulatory Affairs Internship at Johnson & Johnson. This fully remote Internship Opportunity for life science Students in the USA offers hands-on experience in global regulatory submissions, compliance, and healthcare innovation. Ideal for students seeking a high-impact Internship in USA, this role combines regulatory strategy, data analytics, and real-world MedTech exposure.
About the Company
Johnson & Johnson is a global leader in healthcare innovation, operating across pharmaceuticals, medical devices, and consumer health. With a reach of over one billion people daily, Johnson & Johnson is committed to advancing science, equity, and patient outcomes worldwide through cutting-edge research and ethical leadership.
Regulatory Affairs Internship Details:
- Intern Title: Regulatory Affairs Intern
- Requisition Number: R-052864
- Function: Career Programs
- Sub-Function: Non-LDP Intern / Co-Op
- Category: Intern / Co-Op (Non-LDP, C)
- Work Pattern: Fully Remote
- Primary Location: Irvine, California, United States of America
- Application Deadline: January 29, 2026 (may be extended)
Position Overview
Johnson & Johnson MedTech is recruiting Regulatory Affairs Interns for Summer 2026. This internship provides hands-on exposure to regulatory strategy, global product submissions, regulatory lifecycle management, and data analytics within a leading healthcare organization.
Interns will collaborate with Regulatory Affairs professionals, cross-functional teams, and global partners while gaining foundational experience in regulatory compliance across medical devices, pharmaceuticals, and healthcare products.
Key Learning & Responsibilities
- Assist with compilation of requirements for global regulatory submissions
- Support acquisition, organization, and management of regulatory files
- Attend project team meetings with Regulatory Affairs leads and contribute to strategic discussions
- Learn regulatory competencies supporting product registration and lifecycle compliance
- Evaluate current regulatory processes and propose efficiency improvements
- Perform data analytics using Regulatory Information Management (RIM) systems
- Develop reports, dashboards, and presentations
- Support U.S. and Global Regulatory Policy understanding and shaping activities
Qualifications For Regulatory Affairs Internship
Currently enrolled full-time in:
- An undergraduate program (completed at least 2 years), or
- A graduate program (M.S., Ph.D., or M.D.)
Major in a relevant field such as:
- Biomedical, biochemical, life sciences
- Medical or scientific writing
Availability & Eligibility
- Available full-time (40 hours/week) during Summer 2026 (June–July)
- Legally authorized to work in the United States
- Must not require visa sponsorship now or in the future
(CPT, OPT, or STEM OPT candidates typically do not qualify unless eligible for alternative long-term status)
Skills & Competencies
- Proficiency in Microsoft Office:
- Excel (advanced skills including pivot tables and graphs)
- Word and PowerPoint
- Strong written and verbal communication skills
- Familiarity with SharePoint, Teams, and other IT systems preferred
- Ability to work independently and collaboratively
- Curious, flexible, and adaptable mindset
- Proactive, innovative, and confident in sharing ideas
