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Global Reg CMC Lead for Biologics & Enzyme Therapies
Posted 3 days 4 hours ago by Proclinical
Permanent
Full Time
Other
London, United Kingdom
Job Description
Proclinical is seeking a Regulatory Affairs CMC Consultant to lead regulatory strategy and operations for global biologics development and registration. The role involves guiding cross-functional teams, contributing to high-quality submissions, and ensuring compliance with global regulatory requirements.
You will work on biologic products including enzyme replacement therapies, engaging with regulatory authorities to support submissions and post-approval activities, while staying current with
