MES Engineer - Siemens Opcenter Pharma - Belgium - 6+ Months

Brussels, Brussels Capital  ‐ Onsite

Keywords

Pharmaceuticals Workflows Title 21 of the Code of Federal Regulations Enterprise Resource Planning Supervisory Control and Data Acquisition (SCADA) Programmable Logic Controllers Automation Batch Processing Data Integrity Debugging Electronic Data Interchange (EDI) Quality Management System Testing Pharmaceutical Production

Description

We are supporting a client in Belgium in their search for a Siemens Opcenter SME to assist with the commissioning and programming of their Siemens Opcenter Pharma MES. This role is crucial in ensuring a smooth system setup, seamless integration with existing enterprise systems, and compliance with pharmaceutical industry regulations.

Responsibilities:
– Set up and configure Siemens Opcenter Pharma, ensuring compliance with GMP, FDA 21 CFR Part 11, and other industry regulations.
– Connect Opcenter with ERP, SCADA, PLCs, and other automation systems to enable seamless data exchange.
– Develop and customize workflows for batch processing, material tracking, and quality management.
– Program and optimize manufacturing workflows to enhance efficiency and reduce human error.
– Conduct system testing, debug issues, and provide support to ensure smooth operation post-commissioning.

Key Skills:
– Experience in setting up and managing Siemens Opcenter Pharma.
– Knowledge of GMP, FDA 21 CFR Part 11, and data integrity standards.
– Expertise in linking MES with ERP, SCADA, and PLCs.
– Familiarity with pharmaceutical production workflows.
– Ability to diagnose and resolve system issues efficiently.
Start date
ASAP
Duration
6 months
(extension possible)
From
Optimus Search GmbH
Published at
02.04.2025
Contact person:
Marie Bernhard
Project ID:
2865299
Industry
Medicine and Pharmaceuticals
Contract type
Freelance
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