Global Regulatory Affairs Scholar | Two-Year Fellowship

Johnson & Johnson Co.; Raritan (NJ); Hybrid; USD 76,000 - 122,000; Full time

Benefits offered by this job

Hybrid work model

US relocation assistance

Job summary

Johnson & Johnson invites applications for a Global Regulatory Affairs Scholar position in Spring House, PA, or Raritan/Titusville, NJ. The two-year fellowship provides hands-on development with regulatory professionals, multiple rotations across disease-therapeutic areas, and exposure to related regulatory functions.

Under mentorship, you'll tackle real-world projects, grow leadership and cross-functional skills, and complete a capstone project presented to senior leaders.

Qualifications

• Bachelor's degree from a 4-year university program.
• Pursuing an advanced degree (Master’s level) in a scientific, technology or engineering related field with graduation planned by May 2027.
• Early professional experience in regulatory affairs.

Responsibilities

• Develop a broad understanding of the global drug development lifecycle and related strategies for engaging health authorities.
• Learn the laws, guidance and regulatory requirements for drugs and combination products while staying aligned with the organization’s goals.
• Tackle real-world projects that build leadership, influence stakeholders, and enhance collaboration and problem-solving.
• Grow your professional network and cross-functional exposure while working with different teams.
• Own a complex capstone project and present results to GRA senior leaders and other internal partners.

Skills

Analytical Reasoning

Leadership

Regulatory Knowledge

Scientific/Engineering Background

Education

Bachelor's degree in a scientific field

Master’s degree in science/engineering (preferred)

Job description

Johnson & Johnson invites applications for a Global Regulatory Affairs Scholar position in Spring House, PA, or Raritan/Titusville, NJ. The two-year fellowship provides hands-on development with regulatory professionals, multiple rotations across disease-therapeutic areas, and exposure to related regulatory functions.

Under mentorship, you'll tackle real-world projects, grow leadership and cross-functional skills, and complete a capstone project presented to senior leaders.