Regulatory Affairs Summer Intern

Company: Disability Solutions
Location: Raritan
Posted on: September 29, 2024

Job Description:

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/.At Johnson & Johnson Innovative Medicine, we use heart, science and ingenuity to create transformational medicines to improve the health of humanity. Every day, we work to advance scientific research and commercial innovation, to deliver solutions that provide value to patients, physicians and healthcare systems around the world. With a diverse company culture, we celebrate the uniqueness of our employees and are committed to inclusion. We collaborate with the world for the health of everyone in it.Global Regulatory Affairs (GRA) is looking for a high energy, inventive, self-starter intern for its 2025 program. We offer an exciting immersive summer internship experience for individuals who are passionate about exploring a career in healthcare.What's it like to be a Regulatory Affairs Summer Intern?Gain hands-on, real world experience through an extensive overview of the pharmaceutical industry. Work on projects that improve your leadership, problem solving, and critical thinking skills. Network and gain cross-functional exposure. Experience different disease-therapeutic areas, and associated regulatory areas including Product Labeling, Chemistry, Manufacturing and Controls, Policy and Intelligence. Work with knowledgeable mentors and develop skills to build a strong career foundation!During your 10 week internship, you will:

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• Work on programs and strategies for compounds in development and/or marketed products.
• Gain experience and exposure in drug development intended to address unmet medical needs in markets globally through an understanding of laws, guidances, and regulatory requirements for drugs and combination products.
• Use creative problem solving skills to develop new ideas and insights, including takeaways about yourself as a leader.
• Partner with other regulatory interns with diverse skills and experiences in building solutions for real-life business challenges through hands-on projects.\r\r

Keywords: Disability Solutions, Vineland , Regulatory Affairs Summer Intern, Other , Raritan, New Jersey