This role will offer you:

• An opportunity to join a world leader within Cell Therapy and be influential in the direction of the company.

You will be responsible for:

• Lead matrixed teams internally and with CDMOs to support GMP production, including production of plasmid DNA, viral vector, and cell drug product (as required).  
• Identify opportunities for continuous improvement and innovation initiativeto enhance manufacturing efficiency, productivity, and quality.
• Develop and lead cross-functional virtual site teams (VSTs) that include representatives from MSAT, Quality, QC, and Supply Chain and are accountable for product supply from CDMOs
• Proactively identify potential manufacturing risks and challenges and develop contingency plans to address issues that may arise during production.
• Plan, track, and manage manufacturing timelines, deliverables, and budgets for multiple projects simultaneously.

You will bring the following:

• BSc, MSc or PhD in a Scientific or Engineering discipline along with significant industry experience managing external partners.
• Strong knowledge of Cell and Gene Therapy manufacturing processes preferred, biopharma experience essential.
• Familiarity with regulatory standards and quality systems in the biopharmaceutical industry.
• Strong project management, organization, collaboration, and conflict resolution skills and experience.