85 Collaborate to URS definition for calibration needs and ensure process parameter data are available (set point, ranges, resolution, tolerances…) during design phases. Ensure link with Frankfurt legacy plant Calibration SME to advise on some decision making and collect feedback for best integration.
85 Design calibration strategy: Define registration process according to Sanofi Global standards (criticality assessment, maximum permissible error calculations…),
85 Define execution process including labelling, certificates management, compliance status.
85 Lead “blue reviews” based on P&ID and instrumentation documentation with process, MSAT, manufacturing and quality teams to validate compliance parameters.
85 Build and deliver calibration plan with measuring chains inventory, compliance parameters and adapted control frequencies. This for instruments, laboratory equipment and technical checks activities (Environmental control in HVAC systems, thermal mapping…) Ensure implementation of stand-alone calibration software tool. for C&Q phase (initial calibration registration) and its migration to iShift program for routine (periodic calibration) mode with support of CMMS key-user.
85 trajectoiTransfer and implement calibration plans with Beijing local maintenance team and to manage execution plan for initial controls with local resources