A global healthcare leader committed to discovering and developing innovative medicines that improve and extend people’s lives You will be responsible for: Develop, configure, and optimize PAS-X workflows, including Master Batch Records (MBRs) and equipment integration. Manage MES PAS-X deployments, ensuring alignment with production processes and regulatory standards. Work closely with cross-functional teams, including manufacturing, IT, quality, and supply chain, to support PAS-X initiatives. Provide technical support for PAS-X systems, identifying and resolving issues to maintain operational continuity. Create user manuals and provide training for production teams on PAS-X system use and updates. Required Qualifications Looking for people with PAS-X MES experience for Lifecycle management – editing mbr’s, dealing with change control, sometimes change in recipes for different products etc. General hands on maintenance of the PAS-X system. Experience within the pharmaceutical industry is a must but only need a minimum of around 2 years experience. Hands on experience with PAS-X MES Education Bachelor’s degree in Engineering, Computer Science or a related field