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MES Engineer (468)

Realta Technologies

·

Today

Type
Full-time
Department
Engineering
Experience
5+ years
Education
Bachelor
Source
RecruiterFlow

Description

Réalta Technologies are searching for an MES Engineer with over 5 years' experience to support a pharmaceutical client of ours based in Cork.
 
Job Responsibilities
  • Provide day-to-day support for the site's Manufacturing Execution System (MES), ensuring system availability and reliable operation within a GMP manufacturing environment.
  • Troubleshoot and resolve MES-related issues, identifying root causes and implementing sustainable corrective and preventative actions.
  • Support manufacturing operations by investigating system errors, recipe execution issues, electronic batch record (EBR) queries, and interface-related problems.
  • Perform MES configuration updates, system maintenance, and controlled changes in line with site change management procedures.
  • Execute impact assessments, testing, validation, and change control activities for MES enhancements, upgrades, and support requests.
  • Collaborate with Manufacturing, Automation, Quality, Validation, IT, and other cross-functional teams to resolve technical issues and implement continuous improvements.
  • Support the integration and ongoing operation of MES interfaces with systems such as DCS, SCADA, ERP, LIMS, and historians where applicable.
  • Participate in system upgrades, patching activities, and lifecycle management initiatives while ensuring compliance with GMP and data integrity requirements.
  • Develop and maintain MES support documentation, SOPs, work instructions, and technical procedures.
  • Provide technical guidance and user support to manufacturing personnel, assisting with issue resolution and promoting best practices for MES usage.
Job Requirements
  • 5+ years' experience as an MES Engineer within the life sciences industry.
  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related discipline.
  • Strong experience supporting Manufacturing Execution Systems within a GMP-regulated pharmaceutical or biotechnology environment.
  • Hands-on experience with Emerson Syncade is essential, ideally within an API manufacturing environment.
  • Experience supporting electronic batch records (EBRs), MES recipes, system configuration, and change control activities.
  • Proven ability to troubleshoot complex MES issues, perform root cause analysis, and implement effective technical solutions.
  • Experience working with MES integrations to systems such as DCS, SCADA, ERP, LIMS, or other manufacturing systems would be highly advantageous.
  • Strong understanding of GMP, CSV, data integrity, and quality system requirements.
  • Excellent communication and stakeholder management skills, with the ability to work effectively across Manufacturing, Automation, Quality, Validation, and IT teams.
  • A proactive approach to problem solving with strong analytical skills and a continuous improvement mindset.

Skills

GMPSCADAComplianceERPChange Management