Regulatory Affairs Intern at Johnson & Johnson

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.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Zug, Switzerland

Job Description:

Job Title:

Intern (w/m/d) Regulatory Affairs

Location:

Zug, Switzerland

Start:

September 2026

Johnson & Johnson is currently seeking an intern to joinour Regulatory Affairs Team located in Zug Position Overview

Tasks & Responsibilities:

As our Regulatory Affairs Intern, you will support the Swiss Regulatory Affairs (RA) team in bringing innovative medicines to patients by contributing to compliant maintenance of marketing authorizations and regulatory documentation. Fully embedded in the team, you will gain hands-on exposure to the Swiss regulatory landscape, support Swissmedic-related activities, and contribute to product lifecycle management of pharmaceuticals in collaboration with cross-functional partners. Your tasks will include:

• Support lifecycle activities for assigned products (e.g., dossier updates/variations and related documentation) and help track deliverables to meet agreed timelines.

• Maintain regulatory files and trackers, ensuring information is complete, accurate, and audit-ready.

• Support the review of labeling and packaging materials for compliance with Swiss requirements and internal standards.

• Build and maintain working knowledge of relevant regulatory guidelines (e.g., Swissmedic guidance) to support day-to-day RA activities.

• Support compliance activities by following local and global procedures and helping ensure records are maintained in line with requirements.

• Support translations (English to German) and/or review of translations for labeling documents, as needed.

Qualifications

Education and Experience:

• Completed bachelor’s degree or currently enrolled in a master’s program in pharmacy, life sciences, natural sciences, or a related field.

• Genuine interest in regulatory and compliance topics; prior training or first practical exposure (e.g., QA/RA, GMP, documentation) is a plus.

Qualifications

Skills:

• Strong interest in Regulatory Affairs and the pharmaceutical industry.

• Fluent German and very good English; French and/or Italian is an advantage.

• Clear written and verbal communication skills; ability to collaborate effectively across functions.

• Good working knowledge of MS Office (Word, Excel, PowerPoint).

• Structured, analytical approach with the ability to identify issues and propose practical solutions.

• Reliable, proactive, and well organized, with strong attention to detail and comfort working with documentation and deadlines.

Our Offering:

• A 6-month full-time internship in an international healthcare company to grow your professional experience, start date: September 2026.

• Hands-on Regulatory Affairs experience in a world-leading company researching and developing innovative medicines.

• A supportive team environment with a strong sense of belonging.

• Flexible working conditions, including up to 40% remote work (subject to role requirements).

Please mention in your application if you learned about this opportunity through the Health Science Club.Required Skills: Preferred Skills: