MES Systems Engineer for Pharma & Biotech Processes

DPS Group; Dublin; On-site; EUR 60,000 - 80,000; Full time

Job summary

DPS Group is seeking an experienced MES Engineer to drive the development of reliable MES systems and master recipes aligned with our High Product Quality and Lean Manufacturing objectives in Ireland. You will contribute to design, configuration, testing, and validation of MES components.

The role requires collaboration across teams, strong problem solving, and hands-on experience with SAP/LIMS/DeltaV interfaces. A background in biotech/pharma manufacturing is preferred.

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 biotech/pharma.
• Experience in manufacturing information systems/controls in biotech/pharma (desirable).

Responsibilities

• Develop reliable MES system and master recipes to meet process requirements for High Product Quality and Lean Manufacturing.
• Author MES recipes and ensure appropriate MES content changes for facility goals.
• Test and validate MES Recipes and related configurations.
• Create MES deliverables such as design documents and validation activities.
• Develop MES recipes to corporate design standards.
• Perform MES System administration interfacing with SAP/LIMS/DeltaV.
• Syncade build Equipment, Material management, Reports and Inventory Management.

Skills

Communication

Organizational skills

Problem solving

Team collaboration

Project management

Visual Basic

SQL Server

Education

Bachelor's or Master's degree in Engineering / IS / CS / Life Sciences

Tools

Visual Basic

Microsoft SQL Server

Job description

DPS Group is seeking an experienced MES Engineer to drive the development of reliable MES systems and master recipes aligned with our High Product Quality and Lean Manufacturing objectives in Ireland. You will contribute to design, configuration, testing, and validation of MES components.

The role requires collaboration across teams, strong problem solving, and hands-on experience with SAP/LIMS/DeltaV interfaces. A background in biotech/pharma manufacturing is preferred.