International Pharmaceutical Manufacturer are Seeking to Recruit an MES PAS-X Specialist, on a Full-Time, Permanent Basis, at their Steriles Facility in Cheshire

The Main Purpose of this Role is to Provide System Excellence for the Manufacturing Batch Records, (MBR’s) and Manufacturing Execution System, (MES), within Operations to Update and Design New Configuration within the MES System to Align Correctly with the Standard Operating Procedures, (SOP’s) and to Update and Control All Master Data within the MES

ROLE

• Update Manufacturing Batch Records, (MBR’s) in Manufacturing Execution System, (MES), for Existing and New Products, Based on Approved Production Documents
  
  
• Update MBR’s 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
  
  
• Active Involvement in Promoting Site Safety Culture, Raising Safe and Unsafe Conditions or Acts through Channels
  
  
• Support Route Cause Analysis for Fault Finding
  
  REQUIRED
  
  
• Degree in Engineering, Scientific or IT
  
  
• Experience of Using an Enterprise Resource Planning, (ERP), System
  
  
• Experience of System Analysis Program Development (SAP), Manufacturing Processes
  
  
• Experience of Manufacturing Execution Systems, (MES)
  
  
• Knowledge of PAS-X, is Desirable
  
  
• Experience of Working within a Highly Regulated Industry eg Pharma or Related Sector
  
  
• Understanding Quality Guidelines and Regulations, Environment and IT System Validation Process, (GxP)