Senior MES Syncade Engineer – GMP Automation & Interfaces

SimoTech; Cork; On-site; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Autonomy in role

Skills development opportunities

Exposure to large corporate clients

Job summary

SimoTech is hiring an experienced MES Engineer to support a Cork campus for a global pharmaceutical client on site. The role requires 5+ years with Emerson Syncade, strong GMP knowledge, and proven ability to design, implement and test MES recipes and interfaces.

You will contribute to MBR design, system integration with DCS/SCADA/ERP where needed, and participate in cross-functional teams to ensure regulatory compliance and operational efficiency.

Qualifications

• 5+ years' experience as an MES Engineer within the life sciences industry
• Broad technical experience in MES system design, configuration and testing
• Experience with Emerson Syncade within a pharmaceutical API environment
• Strong understanding of GMP manufacturing processes and MES lifecycle

Responsibilities

• Map and develop MES recipes for manufacturing processes
• Lead recipe design sessions with Business Process SMEs
• Test and control MES recipe changes and MBR development
• Configure and test MBRs from design to deployment
• Design interfaces between Syncade MES and third-party systems
• Collaborate with Automation, Lab Systems, ERP and Quality teams on MES
• Support ongoing MES development and improvements to processes
• Train EBR end-users and update SOPs as needed
• Troubleshoot MES interfaces and issues

Skills

MES Engineer

GMP

Communication

Education

Bachelor's degree in engineering, computer science, life sciences, or similar

Job description

SimoTech is hiring an experienced MES Engineer to support a Cork campus for a global pharmaceutical client on site. The role requires 5+ years with Emerson Syncade, strong GMP knowledge, and proven ability to design, implement and test MES recipes and interfaces.

You will contribute to MBR design, system integration with DCS/SCADA/ERP where needed, and participate in cross-functional teams to ensure regulatory compliance and operational efficiency.