Senior EU Regulatory Affairs Specialist (MRP/DCP)

High5, based in Reading, is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for EU medicinal products in a hybrid role. You will manage submissions (MRP/DCP), respond to Health Authority questions, and oversee post-approval commitments and variations.

Ideal candidates have 6+ years in EU regulatory affairs, strong communication skills, and a track record in lifecycle management and non-prescription procedures.

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