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MES Engineer 1227



SimoTech require a MES Engineer with a minimum of 3 years’ experience to work onsite with a key biopharmaceutical client in Dublin. The MES Engineer will be responsible for development, configuration, and testing of MBRs from initial to final design.

Key Responsibilities

  • Primarily responsible for the development, configuration, and testing of MBRs from initial to final design.
  • Take part in MBR development design reviews which includes cross-functional communication and cooperation with other internal engineering and quality groups.
  • Full lifecycle responsibility for the Application Lifecycle Management test scripts and test sets for testing MBR design.
  • Provide support and technical expertise for the ongoing development of the site MES system in development of MBRs and improving the MES business process.
  • Take part in the training of all relevant EBR end-users and the ongoing development, review, and update of all relevant SOPs.
  • Provide technical expertise for equipment integration design, configuration, and testing to allow MBR interaction with shop floor equipment.
  • Carry out troubleshooting and fault-finding where required for MES and all relevant interfaces as required.


  • Minimum of 3 years’ experience in a pharmaceutical environment.
  • Education to a third level degree or equivalent in Engineering or similar.
  • Any experience of working in syringe/Vial manufacturing operations is preferred.
  • Broad technical experience in the delivery of MES systems/projects including design, configuration and testing is essential.
  • Demonstrated ability to learn quickly and adapt to new technology.

What SimoTech Can Offer

  • Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
  • Long term project opportunity.
  • SimoTech can facilitate these positions as a staff engineer or contract engineer.

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