Once trained you will be expected to; work to standards dictated to by Good Manufacturing practice, (GMP) and UKAS 15181 and 17025. use all available IT, and LIMS answer the phone and handle clinical enquirers passing to more senior staff as required, maintain the day to day operation of the department by performing preventative routine daily and weekly maintenance, cleaning equipment, running Quality Assurance, partaking in External Quality Assurance, and re validating (re verification) of equipment once repaired or after Engineer preventative maintenance. monitoring stock levels across sites, maintaining a clean and tidy department as described to by GMP. Accepting deliveries Arranging for transfer of items and confirmation of send/receipt across sites. maintaining your training records monitoring temperatures of our monitored and temperature controlled equipment and department areas by using Tutela and local procedures. reporting all Non-conformance on our Quality Management System using Q Pulse. Please see job description & person specs for full details