Job Title: Senior MES Engineer
Job Type: 23-month Contract
Salary: €60-€72 per hour
Location: Westport
Ref Code: DES-855

KEY REQUIREMENTS

• Third-Level qualification in a relevant manufacturing, engineering, or business-related field, or equivalent experience.
• Minimum of 7 years’ experience in MES authoring, with a proven track record of leadership or technical lead roles in multiple implementation projects.
• Strong proficiency with MES applications, configuration rules, and interfacing (preferably POMSnet).
• Experience in batch processing operations within an FDA/HPRA-regulated environment.
• In-depth knowledge of cGMP and pharmaceutical regulatory requirements.
• Solid understanding of IT systems relevant to MES.
• SAP knowledge/experience in MM, PP, and IM modules is highly desirable.
• Proven ability to maintain high attention to detail and ensure compliance with procedures.
  To discuss this role in more detail, contact Corné at 094 9316002 or corne@dillones.ie for a confidential discussion

• Maintain and author MES recipes and worksheets for the Westport site.
• Provide technical leadership and troubleshooting for MES Engineers, acting as the escalation point for complex issues or recipe design challenges.
• Design, create, and modify MES recipes, worksheets, and material specs, including phase transition logic.
• Develop and execute test protocols, validation procedures, risk assessments, and ensure robust system documentation.
• Align cleaning, equipment, and product procedures with MES processes.
• Deliver training for site personnel, manage system access, and keep teams updated on MES changes.
• Participate in MES knowledge exchanges and MES Governance meetings to share best practices.
• Collaborate with the Global MES team to identify and implement system improvements.
• Support New Product Introduction (NPI) projects, ensuring MES system and hardware requirements are addressed.
• Contribute to continuous improvement initiatives for safety, quality, and operational efficiency.
• Document all activities in line with cGMP requirements.
• Comply with and promote EHS (Environmental, Health, and Safety) standards.