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Senior EU Regulatory Affairs Specialist (MRP/DCP
Job Description & How to Apply Below
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.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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