
Manufacturing Systems Manager
5 days ago
We are seeking a seasoned professional to oversee the successful implementation of our Manufacturing Execution System (MES) and related systems. The ideal candidate will have 6-8 years of experience in the pharmaceutical industry, with a strong background in technical and functional expertise in MES & L2 systems.
The Site SME MES Project is a key role responsible for supporting the implementation of the MES & L2 at our pharmaceutical manufacturing sites. This position ensures that site-specific manufacturing processes are accurately captured and reflected in the global MES solution.
Responsibilities include:
- MES Design and Deployment: Representing site-specific needs during MES design, configuration, and deployment.
- Validation Leadership: Leading IQ, OQ, PQ, UAT, and traceability matrix execution.
- GxP Documentation Management: Managing GxP documentation, including URS, FS, DS, test cases, validation plans/reports.
- MES Product Expertise: Maintaining deep knowledge of MES functionality and architecture.
- Front-End Support: Acting as the first point of contact for MES application issues and user support.
- Training and Adoption: Delivering training and ensuring user readiness for MES usage.
- Data Management: Supporting data collection, migration, and master recipe creation.
- Audit Readiness: Ensuring all documentation and systems are compliant and audit-ready.
Requirements:
- Bachelor's degree in Engineering - Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field.
- Preferred: Master's degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Industrial Automation, Pharmaceutical Technology, or related technical fields.
Additional skills:
- Knowledge of data analytics tools.
- Edge Cloud deployment experience with IoT and IIoT.
- L2 integration with MES.
- MES integration with SAP.
- Understanding of network and databases.
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