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
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Global Reg CMC Lead for Biologics & Enzyme Therapies in London employer: ProClinical
Join a globally recognised biopharmaceutical organisation that prioritises innovation and collaboration in the field of protein science and biologic drug development. With a strong commitment to employee growth, you will have access to continuous learning opportunities and be part of a supportive team dedicated to delivering life-changing therapies. Located in a vibrant area, this role not only offers meaningful work but also a dynamic work culture that values your contributions and fosters professional development.
