Beschreibung
Project is related to implementing EBR solutions for Pharma manufacturing using Rockwell FTPS MES software , creation of solution blueprint, development / modification of EBR solution library, creation of recipe master batch records, integration of MES with Automation Later including Scada, Historian and with ERP systems such as SAP
About role -- MES Validation Lead
Roles & Responsibilities
• Prepare overall MES validation plan
• Experience of creating risk register / RAID log
• Creation of IQ test cases for devices ( Weighing scales, scanners, Printers, etc.) and performing device IQ
• Creation of OQ test scripts; support business users to create PQ Test scripts
• Carry out IQ and OQ test activities
• Log defects found during test execution and track until closure
• Expeirence of working on any Pharma MES implementation validation activities,
• Validation of MES on one of the following platforms: Rockwell FTPS MES software / Werum Pas-X / Siemens OpCenter in Pharma
• Carry out end to end Testing of the MES solution
• Good knowledge of GMP (Good Manufacturing practices of Pharma) and Validated environment of Pharma Manufacturing