Regulatory Specialist (6-9mo) - Medical Devices

Panda International is seeking a Regulatory Specialist for a fixed-term contract in Lausanne, Switzerland, from February to October 2026. This role involves supporting regulatory activities throughout the product lifecycle, working closely with Clinical, Quality, R&D, and Operations teams while focusing on EU MDR and FDA regulatory activities.

The ideal candidate will have 1–3 years of experience in medical device regulatory affairs and familiarity with technical documentation and submissions. Fluency in English is required, and knowledge of French is a plus. Interested candidates can contact directly via email or phone.