Regulatory Affairs Lead – Medical Devices
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Nemera, based in Lyon, is seeking a Regulatory Affairs Manager to lead regulatory and compliance activities for ENTD, Ophthalmic and Inhalation devices across multiple markets. You will report to the Global Regulatory & Compliance Manager and work with development, quality, and manufacturing teams to shape regulatory strategy and lifecycle submissions.
The role requires 8+ years in regulatory affairs within the pharmaceutical or medical device field, strong people leadership, and fluency in