Global Regulatory Affairs Scholar

Johnson & Johnson Co.; Spring House (PA); On-site; USD 76,000 - 122,000; Full time

Benefits offered by this job

Vacation -120 hours/yr

Parental Leave - 480 hours/yr

401(k) retirement plan

Job summary

Johnson & Johnson in Spring House, PA, with eligible locations in Raritan, NJ and Titusville, NJ, seeks a Global Regulatory Affairs Scholar for a two-year experiential fellowship. Rotations across disease areas and regulatory functions, including labeling, policy, and CMC, provide hands-on development.

You will work under mentorship, tackle real-world projects, expand your professional network, and present capstone results to senior leaders.

Qualifications

• Strong academic track record required.
• Preferred knowledge of FDA regulations and submission requirements.
• Interest in regulatory affairs with leadership potential.

Responsibilities

• Understand the global drug development lifecycle and health authority engagement strategies.
• Learn laws, guidance, and regulatory requirements for drugs and combination products.
• Contribute to real-world projects to develop leadership and stakeholder skills.
• Grow cross-functional exposure and collaborate with different teams.
• Participate in internal and external meetings to support responsibilities.
• Own a capstone project and present results to senior leaders.

Skills

Analytical Reasoning

Business Writing

Collaboration

Communication

Data Reporting

Detail‑Oriented

Regulatory Awareness

Regulatory Management

Regulatory Compliance

Regulatory Environment

Education

Bachelor's degree in science/engineering

Advanced degree in science/engineering

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

Professional

All Job Posting Locations

Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job Description

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Global Regulatory Affairs Scholar, located in Spring House, PA, Raritan or Titusville, NJ. This role is eligible for one-way US relocation assistance.

Global Regulatory Affairs Scholar Program Overview

The Global Regulatory Affairs (GRA) Scholar Program at Johnson & Johnson is a two-year experiential fellowship that provides recent university graduates with advanced, hands‑on professional development at one of the world’s leading health care companies. Under the mentorship of J&J regulatory professionals, GRA Scholars complete multiple rotations across different disease‑therapeutic areas, and related regulatory functions, such as Product Labeling, Policy and Intelligence, and Chemistry, Manufacturing and Controls.

You Will Be Responsible For

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

Qualifications / Requirements

Education

Earned a bachelor's degree (B.S. or B.A.) from a 4‑year university program. Earned or is currently pursuing an advanced degree (Master’s level) in scientific, technology or engineering related field from an accredited academic institution with a planned graduation by May 2027. Examples include, biomedical engineering, data analytics/applied statistics, quantitative modeling in biology, pharmacy or other healthcare science. This position is strictly suited for candidates with early professional experience who are looking to develop their careers in regulatory affairs.

Experience and Skills Required

Strong academic track record is required.

Preferred

• Some fundamental understanding of pharmaceutical drug development. Knowledge of current Food and Drug Administration (FDA) regulations, guidelines, and submission requirements is desired.
• Proven leadership capabilities in an organizational setting (campus/community activities) is desired.
• Able to work independently, as well as, be part of a group, with curiosity and flexibility.
• Be self‑motivated, possess a “can do” approach, and courage to speak your voice and suggest innovative ideas.
• Be a creative problem solver, with an interest in exploring the international context of healthcare systems and technology contexts.

Ineligibility for severance.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

Preferred Skills

Analytical Reasoning, Business Behavior, Business Writing, Collaboration, Communication, Confidentiality, Data Reporting, Data Savvy, Detail‑Oriented, Execution Focus, Legal Support, Medicines and Device Development and Regulation, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Risk Assessments

The anticipated base pay range for this position is :

$76,000.00 - $121,900.00

Additional Description For Pay Transparency

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Benefits

• Vacation -120 hours per calendar year
• Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
• Holiday pay, including Floating Holidays -13 days per calendar year
• Work, Personal and Family Time - up to 40 hours per calendar year
• Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
• Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
• Caregiver Leave - 80 hours in a 52-week rolling period10 days
• Volunteer Leave - 32 hours per calendar year
• Military Spouse Time-Off - 80 hours per calendar year

For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits