, you'll lead the CMC Office, driving operational strategy and governance across our development portfolio of small molecules, biologics and emerging modalities. You'll be the conduit between internal teams and external partners, ensuring our medicines are developed efficiently, safely, and to the highest quality standards.
Key responsibilities:
Lead the CMC Office to deliver portfolio outcomes across diverse modalities.
Own external development governance with CDMOs and preferred suppliers.
Represent CMC on Asset/Core teams and drive integration from early development to commercial readiness.
Standardise processes and KPIs across Pharma Development, Technical Operations, and GxP partners.
Develop and deliver training programmes to elevate CDMO engagement.
Influence cross-functional stakeholders and ensure accountability across complex projects.
Knowledge, skills & experience:
Significant experience in CMC Pharmaceutical development with a strong focus on technical outputs and end-to-end exposure from early development to commercial readiness
Master's or PhD in a relevant life sciences subject or equivalent experience
Knowledge of small molecules or biologics is highly preferred
Project management experience, qualification or capability
If you're a collaborative leader with deep CMC expertise and a drive to shape the future of pharmaceutical development, we'd love to hear from you.
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