Global Regulatory Affairs Fellow – Scholar Program

Johnson & Johnson Co.; Hopewell Township (NJ); Hybrid; USD 92,000 - 148,000; Full time

Benefits offered by this job

Hybrid work

Relocation assistance

Pension plan

Job summary

Johnson & Johnson is seeking a Global Regulatory Affairs Scholar in Spring House, PA, Raritan or Titusville, NJ. This two-year experiential fellowship provides recent graduates with hands-on development across regulatory functions, with mentorship and multi-rotations across disease areas.

You will work on real projects, build leadership, and present capstone results to senior leaders, while gaining cross-functional exposure and networking opportunities.

Qualifications

• Bachelor’s degree from a 4-year university program.
• Pursuing or completed an advanced degree (PhD/PharmD) in a science/engineering field with graduation planned by May 2027.
• Strong academic track record with leadership experience in campus/community activities.

Responsibilities

• Develop broad understanding of the global drug development lifecycle and engagement with health authorities.
• Learn regulatory requirements for drugs and combination products while aligning with company goals.
• Tackle real-world projects to build leadership, influence stakeholders, and enhance collaboration and presentation skills.
• Grow professional network and cross-functional exposure by working with different teams.
• Participate in internal and external meetings to support responsibilities.
• Own a complex capstone project and present results to GRA senior leaders and partners.

Skills

Analytical reasoning

Leadership

Communication

Teamwork

Data reporting

Detail-oriented

Regulatory affairs management

Regulatory compliance

Regulatory development

Regulatory environment

Risk assessments

Education

Bachelor's degree

Advanced degree (PhD/PharmD)

Job description

Johnson & Johnson is seeking a Global Regulatory Affairs Scholar in Spring House, PA, Raritan or Titusville, NJ. This two-year experiential fellowship provides recent graduates with hands-on development across regulatory functions, with mentorship and multi-rotations across disease areas.

You will work on real projects, build leadership, and present capstone results to senior leaders, while gaining cross-functional exposure and networking opportunities.