New · posted Oct 25
Johnson & Johnson · Pharmaceuticals
Global Regulatory Affairs Scholar
- Raritan, NJ +2 more
- Hybrid
- Full-time
- Associate & Specialist
The role
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.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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.
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.
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.
What you need
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.
Preferrednice to have
- 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.
Preferred Skillsnice to have
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
Pay and benefits
$76,000 – $121,900 a year
Employer providedThe anticipated base pay range for this position is
$76,000.00 - $121,900.00
Retirement pension and 401(k) savings plan
Vacation, sick time and holiday pay
Parental leave
One-way US relocation assistance
Caregiver and bereavement leave
Volunteer leave
Where you'll work
Raritan, NJ +2 moreHybridOpen in Maps (opens in a new tab)
Also posted for: Titusville, NJ · Spring House, PA
More jobs in Raritan, NJ +2 moreWorking conditions
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
Experience and Skills Required: Strong academic track record is required.
From the posting
About Johnson & Johnson
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
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word
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)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off 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
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.
Job intelligence
The context around this role
Live data · October 26, 2026
Salary intelligence
How the pay compares
This role's midpoint is 8% above the US median for Regulatory Affairs roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US32 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $76,000 | — | $121,900 |
| All US (middle half) | $83,750 | $91,750 | $95,500 |
This role: Johnson & Johnson's own published range. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, October 26, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory Affairs
The general path across 310 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership6
- Regulatory submissions3
- GMP and compliance2
- Lab testing and methods1
- Documentation and SOPs1
- Quality systems and risk1
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 36
- Open roles
- 35
- Distinct roles
- 18
- Locations
By discipline
- Quality23 64%
- Regulatory12 33%
- Compliance & Safety1 3%
By level
- Associate & Specialist13 36%
- Senior & Principal12 33%
- Manager7 19%
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Global Regulatory Affairs Scholar at Johnson & Johnson
Applications close October 30. $76K–$122K a year, employer provided.