Description
MES Engineer required to join a global biotech company for an initial 6 month contract.Role and responsibility:
* Development, configuration and testing of electronic master batch records (eMBRs) from prototype to final design
* 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
* 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
If this is you please apply today.