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:

• Strategic leadership across four main areas; Technology Transfer, Manufacturing Support, Continuous improvement and Innovation.
• Identify opportunities for process improvements, automation, and innovation to enhance manufacturing efficiency, productivity, and quality.
• Collaborate closely with CMC and Quality teams to ensure compliance with cGMP regulations and standards.
• Provide technical expertise and support to manufacturing teams, troubleshooting complex issues, and driving process improvements.
• Foster cross-functional partnerships with R&D, Process Development, Analytical Development, Quality Assurance, Regulatory Affairs, Supply Chain, and Manufacturing to drive efficient and seamless operations.

You will bring the following:

• BSc, MSc or PhD in a Scientific or Engineering discipline along with significant industry experience leading MSAT functions.
• Strong knowledge of Cell and Gene Therapy manufacturing processes.
• Knowledge of risk management strategies in biopharmaceutical production.
• Familiarity with regulatory standards and quality systems in the biopharmaceutical industry.