Work with cross-functional teams to understand and document MES requirements and translate them into system configurations.
Configuration, implementation, programming, commissioning and troubleshooting of the MES software within the manufacturing environment
Integration of MES with other enterprise systems (ERP, SCADA, etc.).
Strong knowledge of system testing, validation, and deployment to ensure seamless MES implementation
Help maintain system documentation, including user manuals, technical specifications, and process flow diagrams.
Support data integrity initiatives and ensure compliance with industry standards and regulations.
MES Deployment support – full life cycle implementation, UAT, Go Live
Preferred Experience:
Understanding of industry standards for MES (Manufacturing Execution Systems), including system lifecycle management and best practices in the Pharma industries
Knowledge of Good Manufacturing Practices (GxP) and experience ensuring compliance in regulated environments.
Experience with Siemens OpCenter execution and various modules for pharmaceutical manufacturing.
Familiarity with regulatory compliance requirements (FDA, EMA, or other relevant regulatory bodies) related to MES implementation and operation.
Understanding of data integrity and security standards in manufacturing, particularly in regulated industries.
Ability to understand and implement validation procedures for MES systems in line with regulatory guidelines.
Proficient in developing and customizing OpCenter solutions to align with manufacturing requirements.
Integration of Opcenter MES with shop floor systems, ERP platforms, and custom applications to streamline manufacturing operations and data flow.
Experience of database management – SQL Server, MYSQL or Oracle etc.
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