MES Editor

The MES Editor role contributes to the digitalization of production processes within a pharmaceutical environment by converting operational workflows into digital batch records and ensuring correct configuration within PAS-X. This position involves supporting various MES initiatives and collaborating closely with production, quality, engineering, and project teams to maintain an efficient and compliant production environment. The role requires applying GMP guidelines and change control procedures while implementing specific production processes such as CIP, SIP, and leak tests.