MES Engineer

Next Generation; Dublin; Vor Ort; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

Next Generation in Dublin is seeking an experienced MES Engineer to contribute to pharmaceutical manufacturing systems. The role focuses on MES configuration, implementation, troubleshooting and system support within a GMP-regulated biopharma environment.

Candidates should have hands-on MES knowledge, exposure to platforms like Emerson Syncade, Werum PAS-X or Siemens Opcenter, and strong problem-solving and cross-functional collaboration skills for digital manufacturing projects.

Qualifikationen

• Experience in MES, Manufacturing Systems, Automation or related engineering disciplines.
• Experience in GMP-regulated pharmaceutical/biopharmaceutical environments.
• Knowledge of MES and electronic batch records (EBR).
• Experience with MES configuration, implementation, troubleshooting or system support.
• Familiarity with MES platforms such as Emerson Syncade, Werum PAS-X, Siemens Opcenter or equivalent.
• Understanding of manufacturing processes, automation systems and digital manufacturing technologies.
• Experience with SAP, DeltaV, LIMS or system integration would be advantageous.
• Knowledge of CSV, GMP documentation and change control would be beneficial.
• Exposure to MES recipe development, system upgrades, NPI or continuous improvement projects.
• Strong problem-solving, communication and cross-functional collaboration skills.

Kenntnisse

MES

Manufacturing Systems

Automation

GMP Environment

EBR / MES data

Configuration & Troubleshooting

CSV / GMP docs

Continuous Improvement

Cross-functional Collaboration

Problem solving

Tools

SAP

DeltaV

LIMS

Jobbeschreibung

Do you have experience in MES Engineering, Manufacturing Systems, Automation or Digital Manufacturing within the pharmaceutical or biopharmaceutical industry?

I'm looking to connect with professionals with relevant technical experience for an upcoming MES Engineer opportunity in Dublin.

Skills & Experience

• Experience in MES, Manufacturing Systems, Automation or related engineering disciplines.
• Experience working within a GMP-regulated pharmaceutical or biopharmaceutical environment.
• Knowledge of Manufacturing Execution Systems (MES) and electronic batch records (EBR).
• Experience with MES configuration, implementation, troubleshooting or system support.
• Familiarity with MES platforms such as Emerson Syncade, Werum PAS-X, Siemens Opcenter or equivalent.
• Understanding of manufacturing processes, automation systems and digital manufacturing technologies.
• Experience with SAP, DeltaV, LIMS or system integration would be advantageous.
• Knowledge of computer system validation (CSV), GMP documentation and change control would be beneficial.
• Exposure to MES recipe development, system upgrades, NPI or continuous improvement projects would be desirable.
• Strong problem-solving, communication and cross-functional collaboration skills.