Job Title: Intern (w/m/d) Regulatory Affairs
Location: Zug, Switzerland
Start: September 2026
Johnson &Johnson is currently seeking an intern to join our 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.