Global Reg Affairs Intern

Johnson & Johnson Innovative Medicine • Raritan, NJ

6d • $24 - $53 • Hybrid

About The Position

Johnson & Johnson is seeking a high energy, inventive, self-starter intern for its 2027 Global Regulatory Affairs (GRA) program. This immersive summer internship offers individuals passionate about healthcare an exciting opportunity to gain hands-on, real-world experience in the pharmaceutical industry. Interns will work on projects designed to enhance leadership, problem-solving, and critical thinking skills, while also gaining cross-functional exposure and networking opportunities. The program provides experience in various disease-therapeutic areas and associated regulatory functions, including Product Labeling, Chemistry, Manufacturing and Controls, and Policy and Intelligence, supported by knowledgeable mentors to build a strong career foundation.

Requirements

• Earned or is currently pursuing an advanced degree in a scientific, technology, or engineering-related field from an accredited academic institution (e.g., biomedical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy, or other healthcare science).
• Strong academic track record.
• Able to work independently and collaboratively as part of a group, demonstrating curiosity and flexibility.
• Possess a “can do” approach, and courage to speak your voice and suggest innovative ideas.
• Available to work full-time (40 hours per week) during the internship.
• Must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g., H1-B status) now or in the future.
• Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long-term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.

Nice To Haves

• Experience/interest in graphic or visual design, journalism, creative writing, or creative arts.
• Demonstrated leadership in campus/community activities.

Responsibilities

• Work on programs and strategies for compounds in development and/or marketed products.
• Gain experience and exposure in drug development intended to address unmet medical needs in markets globally through an understanding of laws, guidance documents, and regulatory requirements for drugs and combination products.
• Use creative problem solving skills to develop new ideas and insights, including takeaways about yourself as a leader.
• Partner with other regulatory interns with diverse skills and experiences in building solutions for real-life business challenges through hands-on projects.

Benefits

• Company sponsored employee medical benefits
• Sick time benefits (up to 40 hours per calendar year; up to 56 hours per calendar year for employees residing in Washington State)
• Consolidated retirement plan (pension)

What This Job Offers

• Job Type: Full-time
• Career Level: Intern