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.