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Global MDR Regulatory Affairs Specialist – Medical Devices

Academic Work Switzerland SA | etoy, Switzerland | Posted June 22, 2026

Position Overview

Academic Work Switzerland SA is seeking a Regulatory Affairs Specialist in Etoy, Switzerland, to oversee regulatory compliance and product lifecycle for medical devices. This role involves collaboration with R&D and Marketing teams globally.

The ideal candidate has experience in regulatory affairs within the medical device industry, advanced knowledge of Medical Device Regulation (MDR), and fluent English communication skills.

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