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CMC Regulatory Manager: Phase 3 Readiness & Global Supply

Apsida Life Science | , , united kingdom, United-Kingdom | Posted June 20, 2026

Position Overview

Apsida Life Science is seeking a skilled professional in the United Kingdom to support CMC program execution in a clinical‑stage biotechnology context. The role involves managing CMC timelines, procurement of clinical supplies, and ensuring compliance with GMP regulations.

The ideal candidate will have at least 5 years of experience in related fields and a Bachelor’s degree in relevant disciplines. This position offers an opportunity to work at the intersection of science and project management.

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