Manager Produkcji

Production Manager Permanent
Reporting to the Head of Production, the post holder will be responsible for the manufacture of GMP grade clinical product for cell therapy clinical trials. The post holder will provide management and leadership to any new or current Production supervisors, scientists and technicians within the team. They will oversee the day-to-day operations of the manufacturing process and work in close partnership with the other departments. In addition, they will also be responsible for ensuring the smooth introduction and technology transfer of all new processes to Production, the performance of the department from a quality and operational perspective and ensure the most effective use and utilisation of the staff and assets at their disposal. The post holder will exercise overall responsibility for good housekeeping, high standards of cleanliness and compliance to GMP procedures in all areas.

Responsible for the manufacture of cell-based therapies for clinical use. Oversee the day-to-day management of all production operations, ensuring that suitable resource and expertise is employed to deliver the service in line with business objectives and regulatory guidelines.
Manage direct reports, assign tasks, monitor performance on a frequent basis and support their personal development including instilling the necessary attitude and behaviours for the achievement of production efficiency and continuous improvement. Organising the team to ensure project milestones are met. Where project milestones cannot be met, responsible for the communication of such instances to line management.
Ensure all manufacturing activities are undertaken in accordance with the registered product requirements and to current regulatory and quality standards.
From a production perspective be responsible for ensuring the appropriate technology transfer of new platforms and products and/or new manufacturing processes and techniques is agreed upon and is implemented successfully to deliver improvement in either safety, quality, capacity or capability of the department. Perform problem solving/trouble shooting of cell culture production processes by identifying issues and implementing procedures in accordance with GMP and relevant regulatory standards and in accordance with QMS.

Familiarity with environmental monitoring systems and experience in organising APS is preferred.
Experience in management and progression of quality records including deviations, change controls and quality risk assessments.