MES Specialist
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Tasks
- Design and configure Master Batch Records (MBRs) for pharmaceutical manufacturing environments.
- Translate manufacturing processes and requirements into compliant and efficient MES solutions.
- Participate in design workshops, reviews, testing, validation and deployment activities.
- Collaborate with manufacturing, process engineering, quality and MES teams in an international project environment.
- Interpret process flow diagrams, P&IDs and manufacturing documentation to develop MES design logic.
- Support standardization, troubleshooting and continuous improvement of MBR solutions, with a focus on reusability, scalability and regulatory compliance.
Requirements
- A few years of experience in a pharmaceutical environment,
- Hands-on experience with MBR configuration and management.
- Previous involvement in MES configuration, development, implementation or support in a manufacturing setting.
- Good English skills.
What we offer
- Attractive base salary above the market average
- An attractive compensation and benefits package with a broad selection of additional employee benefits. Flexible working options,
- Flexible working options, including opportunities for remote work.
- Extensive professional development and training opportunities.
- A range of programs supporting employee well-being, family needs and financial security.
- A stable global environment where you can work with international teams and deepen your expertise.
MES, Manufacturing Execution System, MBR, Master Batch Record, Rockwell, FactoryTalk, PharmaSuite, Rockwell Automation
Referenciaszám: 4173