
MES Engineer
2 weeks ago
Responsibilities
• Design, configure, and deploy MES solutions tailored to pharmaceutical manufacturing processes.
• Collaborate with cross-functional teams including QA, IT, and production to gather requirements and translate them into MES functionalities.
• Develop and maintain electronic batch records and ensure alignment with GMP and regulatory standards.
• Troubleshoot MES-related issues and provide timely support to manufacturing operations.
• Participate in system validation, including authoring and executing test protocols (IQ/OQ/PQ).
• Support continuous improvement initiatives by leveraging MES data analytics and reporting tools.
• Ensure system documentation is up-to-date and compliant with internal and external audit requirements.
Requirements
• Extensive experience in MES implementation within a pharmaceutical manufacturing environment.
• Strong analytical and problem-solving skills.
• Excellent communication and stakeholder management abilities.
• Experience with integration of MES with ERP and LIMS systems.
• Knowledge of automation systems (e.g., SCADA, PLC) and their interaction with MES.
MES
Pharmaceutical Industry
External Audit
Pharmaceutical Manufacturing
ERP
Manufacturing Processes
GMP
Software Engineering
Scripting
JavaScript
Reliability
Manufacturing Operations
SCADA
LIMS
Pharmaceuticals
Stakeholder Management
Data Analytics
Manufacturing
Biopharmaceuticals
Software Development
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