EU Regulatory Affairs Director: Biologics

Blackfield Associates is seeking a Regulatory Affairs Director to enhance EU regulatory capabilities within a global CDMO. This role involves providing strategic guidance and managing regulatory operations for large molecule drug substances and biologics.

The ideal candidate will have 15+ years of regulatory affairs experience, a strong background in biologics development, and proven leadership in matrix environments. This full-time, permanent role is remote-based in the UK, requiring travel (~30%).

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