We are seeking an experienced MES Engineer with strong expertise in Werum PAS-X and Core 3 configuration to support the delivery enhancement and support of MES solutions within a regulated pharmaceutical/biotech manufacturing environment.
The successful candidate will work closely with manufacturing quality validation and automation teams to design and implement robust MES solutions that support electronic batch records process execution and digital manufacturing initiatives.
Key Responsibilities
Design configure and support Werum PAS-X MES solutions within GMP manufacturing environments
Develop and maintain PAS-X Core 3 functionalities including:
Master Batch Records (MBRs)
Electronic Batch Records (EBRs)
Workflow configuration
Materials and resource management
Process parameter integration
Collaborate with cross-functional stakeholders including Manufacturing QA Validation Automation and IT
Support MES deployment activities including commissioning qualification and validation
Execute testing activities including FAT SAT IQ/OQ support and user acceptance testing
Troubleshoot MES issues and provide ongoing operational support
Participate in change control deviation investigations and CAPA activities
Ensure compliance with GMP GAMP5 and 21 CFR Part 11 requirements
Support integration activities between MES and adjacent systems such as SAP LIMS DeltaV or SCADA platforms
Create and maintain technical and functional documentation
Required Experience
Bachelors degree in Engineering Computer Science Life Sciences or related discipline
Strong hands-on experience with Werum PAS-X MES
Proven experience working with PAS-X Core 3
Experience in pharmaceutical or biotech manufacturing environments
Strong understanding of GMP-regulated systems and validation lifecycle
Experience with electronic batch record design and execution
Familiarity with ISA-95 concepts and manufacturing process integration
Experience supporting commissioning and qualification activities
Excellent problem-solving and stakeholder communication skills
Preferred Experience
Experience with PAS-X upgrades or greenfield MES deployments
Knowledge of integration technologies and interfaces
Experience with SAP integration
Familiarity with serialization recipe management or automation systems
Exposure to DeltaV Siemens Rockwell or other automation platforms
MES Engineer Werum PAS-X (Core 3)We are seeking an experienced MES Engineer with strong expertise in Werum PAS-X and Core 3 configuration to support the delivery enhancement and support of MES solutions within a regulated pharmaceutical/biotech manufacturing environment.The successful candidate wil...
MES Engineer Werum PAS-X (Core 3)
We are seeking an experienced MES Engineer with strong expertise in Werum PAS-X and Core 3 configuration to support the delivery enhancement and support of MES solutions within a regulated pharmaceutical/biotech manufacturing environment.
The successful candidate will work closely with manufacturing quality validation and automation teams to design and implement robust MES solutions that support electronic batch records process execution and digital manufacturing initiatives.
Key Responsibilities
Design configure and support Werum PAS-X MES solutions within GMP manufacturing environments
Develop and maintain PAS-X Core 3 functionalities including:
Master Batch Records (MBRs)
Electronic Batch Records (EBRs)
Workflow configuration
Materials and resource management
Process parameter integration
Collaborate with cross-functional stakeholders including Manufacturing QA Validation Automation and IT
Support MES deployment activities including commissioning qualification and validation
Execute testing activities including FAT SAT IQ/OQ support and user acceptance testing
Troubleshoot MES issues and provide ongoing operational support
Participate in change control deviation investigations and CAPA activities
Ensure compliance with GMP GAMP5 and 21 CFR Part 11 requirements
Support integration activities between MES and adjacent systems such as SAP LIMS DeltaV or SCADA platforms
Create and maintain technical and functional documentation
Required Experience
Bachelors degree in Engineering Computer Science Life Sciences or related discipline
Strong hands-on experience with Werum PAS-X MES
Proven experience working with PAS-X Core 3
Experience in pharmaceutical or biotech manufacturing environments
Strong understanding of GMP-regulated systems and validation lifecycle
Experience with electronic batch record design and execution
Familiarity with ISA-95 concepts and manufacturing process integration
Experience supporting commissioning and qualification activities
Excellent problem-solving and stakeholder communication skills
Preferred Experience
Experience with PAS-X upgrades or greenfield MES deployments
Knowledge of integration technologies and interfaces
Experience with SAP integration
Familiarity with serialization recipe management or automation systems
Exposure to DeltaV Siemens Rockwell or other automation platforms