About the role
Key Responsibilities
- Develop and author MES recipes in line with business and manufacturing requirements.
- Configure and maintain MES solutions to support operational excellence and lean manufacturing objectives.
- Participate in MES testing, commissioning, and computer system validation activities.
- Create and maintain MES design documentation and validation deliverables.
- Build and manage MES system components including equipment, materials, inventory, and reporting functionality.
- Support MES administration and integration with third-party systems such as SAP, LIMS, and DeltaV.
- Troubleshoot system issues and implement continuous improvement initiatives.
- Collaborate with manufacturing, quality, validation, and engineering teams to deliver projects successfully.
Required Experience
- Minimum 5 years' experience working as an MES Engineer.
- Bachelor's or Master's degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related discipline.
- Strong experience with MES system design, configuration, and implementation within pharmaceutical or biotechnology environments.
- Experience developing and maintaining MES recipes and workflows.
- Understanding of GMP-regulated manufacturing environments.
- Experience supporting system validation and testing activities.
- Knowledge of process control systems and manufacturing information systems.
- Experience with Emerson Syncade MES, SAP, LIMS, and DeltaV integrations.
- Experience with Microsoft SQL Server and Visual Basic.
Why to apply:
- Opportunity to work with a leading pharmaceutical manufacturer.
- Exposure to large-scale MES projects and advanced manufacturing technologies.
- Collaborative and high-performing engineering environment.
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