MES Engineer

Atrium; Dublin; Vor Ort; EUR 121.000 - 163.000; Vollzeit

Zusammenfassung

Atrium in Dublin is seeking an experienced MES Engineer to support a major pharmaceutical/biotech manufacturing environment. You will develop and maintain MES systems and master recipes to ensure high product quality and efficient operations.

This 12-month LTD contractor role offers €70 per hour, 39 hours per week, with a Dublin-based on-site work model.

Qualifikationen

• 3+ years' experience as an MES Engineer.
• Experience in MES system design, configuration and recipe development.
• Experience in pharmaceutical or biotech industry.
• Knowledge of MES validation, testing and GMP environments.
• Experience with Emerson Syncade is advantageous.
• Experience with MES interfaces such as SAP, LIMS and/or DeltaV.
• Knowledge of Visual Basic and Microsoft SQL Server is desirable.
• Engineering, Information Systems, Computer Science, Life Sciences degree.
• Strong communication, problem-solving and project management skills.

Aufgaben

• MES recipe authoring and configuration.
• Supporting CSV validation and MES testing.
• MES system administration and configuration.
• Building/configuring equipment, materials, reports and inventory management.
• Supporting integrations with SAP, LIMS and DeltaV.
• Collaborating with manufacturing, engineering, quality and technical teams.

Kenntnisse

MES design

Configuration

Recipe development

CSV validation

Visual Basic

SQL Server

Pharma knowledge

Project management

Ausbildung

Engineering degree

Tools

Emerson Syncade

SAP

LIMS

DeltaV

Jobbeschreibung

We are recruiting an experienced MES Engineer to support a major pharmaceutical/biotechnology manufacturing environment in Dublin.

Location: Dublin, Ireland

Contract: 12 months

Rate: €70 per hour

Hours: 39 hours per week

Engagement: LTD Company Contractor

The Role

You will be responsible for developing and maintaining robust MES systems and master recipes, supporting high product quality, compliant manufacturing and operational efficiency.

Key responsibilities include:

• MES recipe authoring and configuration
• Supporting Computer System Validation (CSV) and MES testing
• MES system administration and configuration
• Building/configuring equipment, materials, reports and inventory management
• Supporting integrations with systems such as SAP, LIMS and DeltaV
• Working collaboratively with manufacturing, engineering, quality and technical teams

What We’re Looking For

• 3+ years' experience as an MES Engineer
• Strong experience in MES system design, configuration and recipe development
• Experience within the pharmaceutical or biotechnology industry
• Knowledge of MES validation, testing and regulated/GMP environments
• Experience with Emerson Syncade would be highly advantageous
• Experience with MES interfaces such as SAP, LIMS and/or DeltaV
• Knowledge of Visual Basic and Microsoft SQL Server is desirable
• Degree in Engineering, Information Systems, Computer Science, Life Sciences or a related discipline
• Strong communication, problem-solving and project management skills

If you have strong hands-on MES engineering, recipe authoring/configuration and validation experience within Pharma/Biotech, I’d be keen to hear from you.