Description
A Global Biotech organisation currently requires an experienced MES Engineer to work at their facility in Ireland.They are looking for someone who can develop, configure and test electronic Master Batch Records (eMBRs) from prototype to final design.
Responsibility:
-EBR Prototype development to support Design Reviews and key liaison with Production, Technical and Quality functions
-Preparation of eMBR design documentation
-Assistance with drafting and executing of eMBR Pre-Production (OQ) and Production (PQ) and Post-Production (Change Request) protocols and test scripts
-Training of EBR End-users (Supervisors, Operators, Technical/QA/Support staff)
-Equipment integration design, configuration and testing to allow EBR interaction with shop floor equipment
-Liaison with corporate MES core-team to troubleshoot and develop new ways of working
-Ongoing change management of eMBRs based on end-user feedback
Experience Required:
-MES experience with focus on workflow, S95 & S88 standards and integration from the control layer to ERP via MES in pharma & bio-pharma industries
-Managing and delivering MES project as per required milestones
-On-call EBR production support to assist in prompt issue resolution where required
-Continuous improvement attitude to improve operations Education
-Degree in Science, Engineering or IT or equivalent experience
-Three to Five years extensive MES experience within a manufacturing environment
An excellent long term contract opportunity working for a World Leading Biotech organisation.