A Day In The Life Of A MES PAS-X Specialist
The main purpose of this role is to provide system excellence for the MBR (Manufacturing Batch records) & MES (Manufacturing Execution System) within operations, this will cover all areas within PFS (Pre-filled Syringes) and BFS (Blow Filled Seal), to update and design new configuration within the MES system to align correctly with the SOP’s (Standard Operating Procedures) for the governance and manufacture of the medicines produced at Teva. To update and control all master data within the MES. To develop and update the MES where required to support ongoing development of the operations site.
Key Responsibilities:
Update MBRs in MES system for existing and new products based on approved production documents.
Update MBRs with functionality based on site requirements.
Evaluate product change controls and impact on MES / MBR.
Validation for upgrades and SOP/ WI updates
Update / creates SOP / WI for MES.
Support training of new and existing staff.
Have an active involvement in promoting site safety culture raising safe and unsafe conditions or acts through the correct channels.
Support route cause analysis for fault finding.
Who We Are Looking For
Do you have?
Degree in relevant field is preferred but not essential (engineering, IT, Scientific)
Experience of using an ERP system
Current/previous user of SAP manufacturing processes
Practical knowledge about MES PAS-X, Operations and Design.
Relevant Pharma experience or another highly regulated industry, in relation to business processes.
Understanding IT system lifecycle in GxP environment and IT system validation process.
Are you?
Good communicator / motivator / team player.
Able to deliver high performance standards.
If so – we would value hearing from you!
