Internship - Regulatory Affairs (6 months), Lonay

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

Proficiency in MS Office tools (Word, Excel, PowerPoint)

Fluent in English (written and spoken)

Ability to work effectively in cross-functional teams

Well-organized, able to manage multiple tasks, and work independently under tight deadlines

Precision in reviewing technical documentation

Education&Qualifications

Currently pursuing a Bachelor’s or Master’s degree in a field related to life sciences, pharmacy, or related field (Bachelor’s degree preferred)

What We Offer

Work-life balance: flexible working hours and home office where appropriate, plus generous annual leave

Ongoing training: access to multiple training programs (e.g., LinkedIn Learning, FranklinCovey, Harvard online) and development opportunities

Benefits: premium accident insurance, attractive Pension Fund, discounts programs, Employee Assistance Program, and regular team activities

Sustainable development: Merz Group is investing at every site to achieve carbon neutrality by 2035

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