MES Master Batch Records Engineer for Pharma Ops

Akkodis; Antwerpen; Sur place; EUR 65 000 - 90 000; Plein temps

Résumé du poste

Akkodis Belgium is seeking a Senior MES/ERP Specialist to design, validate and maintain Master Batch Records within the Siemens OpCenter Execution Pharma MES ecosystem. You will translate pharmaceutical production processes into robust master data, ensuring compliance with GMP and quality standards across MES, ERP and related databases.

You will collaborate with production, QA, IT and automation teams to define requirements, implement changes, and support continuous improvement while maintaining

Qualifications

• Master's degree in a scientific discipline or equivalent experience.
• Strong interest in MES/ERP systems and interfaces in regulated environments.
• Excellent analytical skills to translate complex workflows into robust Master Batch Records.
• Right-first-time mindset; accurate configurations, changes and documentation for MBRs.
• Proactive, independent planning and organizational skills with ability to meet deadlines.
• Willingness to participate in an on-call service with rotating schedule.
• Excellent Dutch and English, both written and spoken; strong communication with diverse stakeholders.
• Experience in regulated pharma/production environments is advantageous.
• Knowledge of SQL, Python, SCADA, PLC or related automation languages; familiarity with Lean/Six Sigma is beneficial.

Responsabilités

• Translate production processes into Master Batch Records and related master data, following quality standards.
• Design, install, test, document, and validate MBRs and master data across MES, ERP and databases.
• Collaborate with production and quality to define project requirements and timelines for new or modified lines and applications.
• Apply GMPs, SOPs and work instructions in MBR design and change activities.
• Lead or participate in quality improvement projects across site teams.
• Provide user support and training for MBRs, including occasional after-hours assistance.
• Coordinate with IT and automation to ensure proper integration of MBRs with MES/ERP systems.
• Manage smaller MBR changes within agreed deadlines with right-first-time execution.
• Maintain daily interdepartmental and occasional international contacts to align requirements.

Formation

Master's degree in a scientific discipline or equivalent

Outils

SQL

Python

SCADA

PLC

Lean Six Sigma

Description du poste

Akkodis Belgium is seeking a Senior MES/ERP Specialist to design, validate and maintain Master Batch Records within the Siemens OpCenter Execution Pharma MES ecosystem. You will translate pharmaceutical production processes into robust master data, ensuring compliance with GMP and quality standards across MES, ERP and related databases.

You will collaborate with production, QA, IT and automation teams to define requirements, implement changes, and support continuous improvement while maintaining