Intern (W/M/D) In Regulatory Affairs

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

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Job Description:

Internship

Job Title: Intern (w/m/d) in Regulatory Affairs

Location: Zug, Switzerland

Start: 01.08.2025

Johnson & Johnson is currently seeking an intern to join our Regulatory Affairs Team located in Zug

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.

Join us to advance the future of human health and take the first steps toward building a career with a purpose.

Position Overview - Tasks & Responsibilities:

As our Intern, you will be trained as Regulatory Affairs Manager in a Swiss affiliate. You will become an integral part of our dynamic Regulatory Affairs Team. Your experience will be diverse with tasks that include: :

• Supporting of Regulatory Affairs Manager in lifecycle-related submissions for pharmaceuticals, including CMC variations, label updates, PSUR submissions, renewals and safety signal notifications.
• Reviewing of product information, patient leaflets and packaging materials to ensure they meet our high standards.
• Print approvals of packaging materials to maintain consistency and compliance.
• Collaborating closely and actively with local and regional teams.
• Ensuring compliance with all applicable regulations and guidelines.

If you are passionate about making a difference in the pharmaceutical industry and eager to learn from experienced professionals, we want to hear from you!

Qualifications - Education and Experience:

• A completed PhD/master’s degree in pharmacy or natural science (or a related field)

Qualifications - Skills:

• A high level of passion and a keen interest in the pharmaceutical industry
• Desire to grow and develop in a new environment
• Proficient in German and English, both written and spoken, French and/or Italian are a plus
• Exceptional attention to detail and ability to manage multiple projects simultaneously
• Team spirit, creativity, proactivity

Our Offering:

• 12 months full time internship in an international healthcare company to grow your professional experience, start date 1st August 2025
• Training as Regulatory Affairs Manager
• Be part of a world-leading company
• Great team and excellent sense of belonging
• Flexible working conditions with the opportunity of 40% remote work if the job allows