MES Engineer

QCS Staffing; Dublin; On-site; EUR 55,000 - 75,000; Full time

Job summary

QCS Staffing seeks a MES Engineer for an Ireland, Dublin-based 12-month contract in the life sciences sector. The role focuses on hands‑on MES activities within a major facility development, offering exposure to innovative equipment and modern pharmaceutical technologies.

You will author MES recipes, support validation activities, and contribute to key deliverables such as design documents, aligning with corporate design standards and quality goals.

Qualifications

• Proficiency communicating and collaborating at a variety of levels.
• Excellent organisation and planning skills.
• Problem solving, critical thinking and project management ability.
• Proven success of working well in a team environment with flexibility to react to changing business needs.

Responsibilities

• Performing MES recipe authoring activities to ensure appropriate MES content and changes to meet the facility goals of High Product Quality and Lean Manufacturing.
• Participating in the testing and computer system validation of the MES Recipes and related configuration.
• Actively participating in the creation of MES deliverables such as design documents and validation activities.
• Developing MES recipes to corporate design standards.

Skills

Communication

Organization

Problem solving

Project management

Tools

MES (Manufacturing Execution System)

Job description

MES Engineer – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Are you a MES Engineer looking for your next assignment in Dublin? A leading multinational in Ireland’s thriving biopharma industry requires support for their major facility development.

MES Engineer – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Are you a MES Engineer looking for your next assignment in Dublin? A leading multinational in Ireland’s thriving biopharma industry requires support for their major facility development.

This project provides hands‑on experience with innovative equipment, large‑scale operations and modern pharmaceutical technologies. It’s an ideal opportunity to build your skills within one of Europe’s fastest‑growing life‑science regions.

What You’ll Do

• Performing MES recipe authoring activities to ensure appropriate MES content and changes to meet the facility goals of High Product Quality and Lean Manufacturing.
• Participating in the testing and computer system validation of the MES Recipes and related configuration.
• Actively participating in the creation of MES deliverables such as design documents and validation activities.
• Developing MES recipes to corporate design standards.

What you’ll need:

• A proficiency communicating and collaborating at a variety of levels
• Excellent organisation and planning skills.
• Problem solving, critical thinking and project management ability
• Proven success of working well in a team environment with flexibility to react to changing business needs