Senior Digital Manufacturing Specialist

3 days ago

Dublin, Dublin City, Ireland beBeeEngineering Full time €60,000 - €100,000

Job Opportunity:

We are seeking a highly experienced MES engineer to support our client site on a contract basis.

This is a high-impact role offering the chance to contribute to cutting-edge digital manufacturing processes within a globally recognised facility. You'll be working as part of a team of MES professionals delivering robust solutions that directly support batch execution and product release.

About the Role:

The successful candidate will work closely with our team and play a critical role in delivering automation expertise across the site. The ideal candidate will have 5+ years' experience delivering MES solutions in GMP life sciences manufacturing, with strong hands-on experience using Emerson Syncade.

Your Responsibilities:

  • Configure and implement Syncade MES workflows, master batch records (MBRs), and user interfaces tailored to site-specific manufacturing processes
  • Translate manufacturing process requirements into structured MES design specifications and recipes
  • Liaise with process engineers, QA, and operations to ensure that MES solutions align with regulatory and operational standards
  • Support integration between MES and external systems including DeltaV, SAP, and LIMS, ensuring reliable data flow and traceability
  • Develop and maintain validation documentation (URS, FS, DS, IQ/OQ/PQ), supporting audits and data integrity requirements
  • Provide ongoing system support and troubleshooting, including deviation handling, root cause analysis, and system performance tuning
  • Contribute to continuous improvement initiatives by identifying opportunities to enhance MES performance and usability

Requirements:

  • 5+ years' experience delivering MES solutions in GMP life sciences manufacturing, with strong hands-on experience using Emerson Syncade
  • Proven capability in MBR development, recipe design, and configuration of Syncade modules (materials management, equipment tracking, work instructions, etc.)
  • Good working knowledge of cGMP, GAMP5, and 21 CFR Part 11 principles
  • Experience collaborating in cross-functional teams across manufacturing, quality, automation, and IT disciplines
  • Strong documentation and communication skills with the ability to manage priorities in a dynamic, production-critical environment
  • Experience working at or supporting large-scale biologics or vaccine manufacturing sites
  • Familiarity with eBatch release, electronic logbooks, and batch genealogy within MES environments
  • Exposure to validation planning, audit preparation, and supporting CAPAs or change controls

What We Offer:

  • A competitive hourly rate based on experience
  • Flexible working hours may be accommodated in line with project requirements
  • Opportunity to work on a high-profile biopharma site with a collaborative, technically strong team
  • Chance to be part of our network of engineering professionals, contributing to impactful automation solutions in the life sciences sector

Equal Opportunities Employer:

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