Description:

• 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.

Benefits:

• 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
If you are interested in the position, you can submit your application by clicking the "JELENTKEZEM" button!