Réalta Technologies are searching foranMES Engineer to join our team, supporting a prominent pharmaceutical client's manufacturing operations.
This role is focused on the configuration, deployment, and support of the Manufacturing Execution System (MES), specifically in the areas of column packaging, media preparation, and buffer preparation.
The ideal candidate will play a key role in enhancing manufacturing processes, ensuring data integrity, and supporting end-to-end production throughPAS-X MES.Key ResponsibilitiesPAS-X Configuration & Support: Configure, deploy, and maintain PAS-X MES to support manufacturing processes, including column packaging, media, and buffer preparation.Process Optimization: Collaborate with production and engineering teams to analyze and optimize MES-related workflows for efficiency, accuracy, and regulatory compliance.Documentation & Validation: Develop, review, and maintain system documentation, including user requirements, functional specifications, SOPs, and validation protocols, in line with GxP standards.Troubleshooting & Technical Support: Provide day-to-day MES support to end users, addressing system issues, troubleshooting errors, and implementing corrective actions.System Upgrades & Enhancements: Assist in system upgrades, testing, and the rollout of new PAS-X features or modules, ensuring minimal impact on operations.Training & Knowledge Transfer: Train production staff on MES functionalities and provide ongoing support to ensure effective use of the system.Compliance & Quality Assurance: Ensure all activities comply with relevant regulatory and quality standards, including GMP, FDA, and GAMP5 guidelines.QualificationsBachelor's degree in Engineering, Computer Science, Information Technology, or related field.Minimum of 3-5 years of experience as an MES Engineer, preferably in a pharmaceutical or biotech environment.Hands-on experience with PAS-X MES system is essential.Proficiency in PAS-X MES configuration, customization, and troubleshooting.Strong understanding of pharmaceutical manufacturing processes, especially around column packaging, media preparation, and buffer preparation.Knowledge of GxP, GMP, FDA, and other regulatory requirements in the pharmaceutical industry.Excellent problem-solving skills with a proactive approach to troubleshooting.Strong communication skills and ability to work effectively with cross-functional teams.Detail-oriented, with a strong commitment to documentation and quality.
#J-18808-Ljbffr