MES Specialist

Join our partner, an international technology organization supporting the digital transformation of highly regulated manufacturing environments, as a MES Specialist. In this role, you will contribute to pharmaceutical MES projects, turning production processes into effective digital manufacturing workflows.

MES Specialist

Key Responsibilities

• 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 Our Partner Offers

• 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.

Location: Hungary, hybrid / remote opportunity