Global Regulatory Affairs Fellow — Hybrid Program

Biopharma Careers; Raritan (NJ); On-site; USD 92,000 - 148,000; Full time

Job summary

Johnson & Johnson in the United States seeks a Global Regulatory Affairs Scholar for Spring House/ Raritan/Titusville locations. This two‑year fellowship offers rotations across disease areas, with mentorship from regulatory professionals and exposure to labeling, policy, and CMC functions.

The role develops leadership, problem-solving and cross-functional collaboration, with relocation support and a pathway to regulatory affairs careers at a world‑leading health company.

Qualifications

• Bachelor's degree from a 4-year program or pursuing an advanced degree with planned graduation by May 2027.
• Early professional experience in regulatory affairs.
• Strong academic track record and interest in regulatory development.

Responsibilities

• Develop understanding of global drug development lifecycle and regulatory strategies.
• Learn FDA regulations, guidelines, and submission requirements.
• Tackle real-world projects to build leadership, collaboration and problem-solving skills.
• Participate in meetings and support responsibilities across teams.
• Own a capstone project and present results to senior leaders.

Skills

Analytical Reasoning

Regulatory Knowledge

Communication

Teamwork

Education

Bachelor's degree (B.S. or B.A.)

Pursuing advanced degree (PhD/PharmD)

Job description

Johnson & Johnson in the United States seeks a Global Regulatory Affairs Scholar for Spring House/ Raritan/Titusville locations. This two‑year fellowship offers rotations across disease areas, with mentorship from regulatory professionals and exposure to labeling, policy, and CMC functions.

The role develops leadership, problem-solving and cross-functional collaboration, with relocation support and a pathway to regulatory affairs careers at a world‑leading health company.