MES Engineer: Build Robust Pharma Process Systems

Arcadis; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

Arcadis Ireland seeks an experienced MES Engineer to develop reliable MES systems and master recipes, supporting High Product Quality and Lean Manufacturing goals. You will author MES content, validate configurations, and support third‑party interfaces, contributing to projects across biotech/pharma operations.

Ideal candidates hold a technical degree and 3–7 years in MES engineering, with hands‑on experience in MES systems design, configuration, and manufacturing process applications.

Qualifications

• Bachelor's or Master's degree in Engineering, Information Systems, Computer Science or Life Sciences
• 3-7 years experience as an MES Engineer
• Experience with MES System Design, Configuration and Application of business processes in biotechnology/pharmaceutical industries (desired)

Responsibilities

• Performing MES recipe authoring to ensure MES content aligns with facility goals for high product quality and lean manufacturing
• Participating in testing and computer system validation of MES Recipes and related configuration
• Creating MES deliverables such as design documents and validation activities
• MES System administration to third-party interfaces (e.g., SAP, LIMS, DeltaV)
• MES System Syncade build including Equipment, Material management, Reports, Inventory Management
• Communicating and collaborating across levels with excellent organizational and planning skills
• Problem solving, critical thinking, and project management in a team environment
• Experience with Visual Basic and Microsoft SQL Server is desirable

Skills

MES System Design

Process Controls

Team Collaboration

Project Management

Education

Bachelor or Master in Engineering/IS/CS/Life Sciences

Tools

SQL Server

Visual Basic

DeltaV

LIMS

SAP

Job description

Arcadis Ireland seeks an experienced MES Engineer to develop reliable MES systems and master recipes, supporting High Product Quality and Lean Manufacturing goals. You will author MES content, validate configurations, and support third‑party interfaces, contributing to projects across biotech/pharma operations.

Ideal candidates hold a technical degree and 3–7 years in MES engineering, with hands‑on experience in MES systems design, configuration, and manufacturing process applications.