Position Snapshot

• Location: Lonay (Vaud, Switzerland)
• Activity rate: full-time
• Type of contract: 6-month fixed-term internship contract

Key Responsibilities

The Regulatory Affairs Trainee supports the preparation, review, and submission of regulatory documentation and helps coordinate ongoing registration activities. The role contributes to QMS remediation actions following process updates and ensures all related documentation is correctly revised. It also includes participating in the regulatory review of marketing and promotional materials and coordinating with internal stakeholders to implement required changes. Additionally, the trainee manages regulatory documentation in the eQMS, performs technical file reviews, and maintains organized and compliant regulatory records.

What Will Make You Successful

Knowledge & Skills

• Knowledge in Medical Device Industry and Regulatory Affairs
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