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MES Validation Engineer

Archer Recruitment
Department:Operations
Type:HYBRID
Region:Limerick
Location:Limerick, County Limerick, Ireland
Experience:Mid-Senior level
Salary:€400 - €550
Skills:
MESVALIDATIONGXPPHARMACEUTICALMANUFACTURING
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Job Description

Posted on: July 8, 2026

MES Validation Engineer – Greenfield Pharmaceutical Project

  • €400–€550 per day
  • 6-month contract
  • Mulitnational Pharma Company

This role is with one of the largest pharmaceutical organisations globally, who are embarking on a major greenfield MES implementation programme as part of a wider manufacturing technology transformation. They are seeking an experienced MES Validation Engineer to support the delivery and validation of a new Manufacturing Execution System within a highly regulated production environment.

This is a long-term programme of work that will run for several years, offering the opportunity to join at an early stage and play a key role in the implementation, validation, and optimisation of a business-critical platform. You will work closely with manufacturing, quality, automation, and engineering teams to deliver robust MES solutions that support next-generation pharmaceutical manufacturing operations.

This is a fantastic opportunity for an experienced MES Validation Engineer to embed themselves within a high-performing technical environment, gaining exposure to a large-scale greenfield project with significant long-term scope and impact.

Why You'll Love It Here

  • Work on a multi-year greenfield MES transformation programme for a global pharmaceutical leader
  • Join a highly technical environment delivering next-generation manufacturing technology
  • Long-term project roadmap with significant scope for continued involvement

Responsibilities

  • Execute MES validation activities including protocol development, test execution, and documentation
  • Support the implementation and qualification of MES solutions within a regulated GxP environment
  • Collaborate with cross-functional teams across quality, manufacturing, automation, and engineering

Requirements

  • Strong MES validation experience within pharmaceutical or regulated manufacturing environments
  • Experience with GxP validation processes, documentation, and regulatory compliance
  • Knowledge of MES platforms and manufacturing systems implementation

Contract Details

  • Day rate: €400–€550 per day
  • Contract length: 6 months
  • Location: Limerick
  • Working model: Hybrid
  • Extension likelihood: Strong (multi-year greenfield programme)
Originally posted on LinkedIn

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