MES Recipe Author

Role/Job Title: MES Recipe AuthorFind out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now.Work Location: Newbridge, IrelandMode of Working: Office basedAny other working conditions (travel/on call/shifts): Travel to sites in Ireland based on requirementThe Role MES Recipe Author for pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)Your responsibilities: (Up to 10, Avoid repetition) Execution and coordination of responsibilities that include Master Recipe creation, master data creation, maintenance and control of MES activities (Recipe and workflow designer, PMC, PEC, PRC and Data manager Clients).Process mapping (visio), Recipe designing, Testing, Dry runs and Business verification of the created recipes.Understanding of pharmaceutical manufacturing processes (Solid oral dose and packaging preferred)Possesses expertise in Good Documentation and Good Testing PracticesBuilding, Testing and verifying of recipes which require Integration (SAP, gLIMS, catalyst etc).Coordination with core and site teams for new site-specific requirements.Ability to work with site SMEs to turn paper batch records into EBRs in Rockwell Pharmasuite utilizing existing functionalityAbility to work with site SMEs to turn existing EBRs in legacy systems (P2C2, PMX, etc.) into Rockwell Pharmasuite EBRs utilizing existing functionalityAbility to design Building Blocks that can be reused in multiple processesAbility to work in a fact paced agile team environmentPreparing and conducting UAT, Change management, Validation Documentation, User trainingYour ProfileEssential skills/knowledge/experience: (Up to 10, Avoid repetition) Expert in PharmaSuite and specific functionalities.Participates in fit gap analysis & Process Modeling & process standardization xjdpvnf with Area lead & Process SMEWorks with lead RA to develop BB requirementsProvide times, user story point estimates, and status for all stories assigned to themAuthors and performs documents supporting validation of EBRsConfigures EBR in Development, Stage, & Production EnvironmentAddress Site specific questions, use cases and ER from Site EBR and POWorks across the teams to put requirement together for ER developmentProvide HyperCare and Go-live supportExperience: 9+ YearsIf you want, I can also create a standard submission format template

Created: 2026-03-18