Global Regulatory Affairs Scholar

Johnson & Johnson Co.; Raritan (NJ); Híbrido; USD 76.000 - 122.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work model

US relocation assistance

Descripción de la vacante

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.

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Analytical Reasoning

Leadership

Regulatory Knowledge

Scientific/Engineering Background

Educación

Bachelor's degree in a scientific field

Master’s degree in science/engineering (preferred)

Descripción del empleo

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.

#LI-Hybrid 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.

Required Skills: 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)). 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

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 https://www.jnj.com/.