Supervise and ensure staffs are working in accordance with cGMP standard and Standard Operating Procedures. Ensure that the operation is well maintained and all processes are performed in accordance with cGMP. Ensure that the inventory of supplies is accurately maintained with the supporting documentation. Ensure that all personnel are adequately trained and that training records are maintained. Ensure the Singapore facility has sufficient capacity and resource to support daily activities, including critical support. Responsible for all operational duties and process improvement in the operations. Responsible for conducting investigations, change control, risk assessment, and ensure business continuity. Responsible for running Tier process and metrics reporting. Responsible for facility and operations projects management.
Oversee and be responsible for managing all aspects of clinical trials supplies packaging, including supply forecast, batch record production, label production, and execution of the packaging exercise.