EMEA Regulatory Affairs Lead – Medical Devices

CooperVision is seeking a Principal Regulatory Affairs Specialist to lead regulatory direction across the UKI, BeNeLux and Nordic clusters, from concept to launch and post market. You will manage submissions, maintain regulatory files, and interact with government bodies to ensure compliance with UK, EU, ACE and MENA requirements.

Strong technical writing and cross‑functional leadership are essential for this role.

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