Post-Doctoral - Global Regulatory Affairs Scholar

Johnson & Johnson Innovative Medicine is recruiting for Post-Doctoral - Global Regulatory Affairs Scholar.

The position can be located on-site/hybrid in the US (Titusville, NJ; Spring House, PA; Raritan, NJ).

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 https://www.jnj.com/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.

Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.

Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.

Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Global Regulatory Affairs (GRA) is looking for a high energy, inventive, self-starter who is passionate about exploring a career in healthcare.

This position is crafted for candidates who recently graduated, or currently pursuing an advanced degree program (PharmD or PhD).

What's it like to be a Regulatory Affairs Post-Doctoral Scholar?

GRA is a key strategic partner supporting global R&D initiatives at Janssen.

Gain a broad understanding of the global drug development process and related health authority engagement strategies.

Through hands-on, real world experiences, work on projects that improve your leadership, problem solving, and creative and critical thinking skills.

Network and gain cross-functional exposure.

The two-year GRA Scholar Program - known as a fellowship in other companies - starts in Summer 2025.

You will experience different disease-therapeutic areas, and associated regulatory areas, such as Product Labeling, Chemistry, Manufacturing and Controls, Policy and Intelligence.

Attend internal and external cross-functional meetings in support of the role's responsibility.

Work with knowledgeable mentors and develop skills to build a strong career foundation!

You will:


* Gain experience and exposure to groundbreaking programs and strategies for compounds in development and/or marketed products intended to address unmet medical needs in markets globally.

Learn the laws, guidances, and regulatory requirements for drugs and combinatio...