MES Integration Specialist (Werum PAS-X)

Location: Full remote from Warszawa, Poland

Company

hirify.global is an IT consultancy firm delivering software design, development, implementation, and integration services for startups, mid-sized companies, and large corporations across multiple industries.

What you will do

• Provide Level 2 support for MES applications across pharmaceutical manufacturing and packaging operations.
• Troubleshoot MES incidents, execution issues, interface failures, and production support requests.
• Perform root cause analysis and collaborate with L3 teams, vendors, and business stakeholders on complex issues.
• Support and maintain integrations between Werum PAS-X, SAP PP-PI, ERP, and other manufacturing systems.
• Administer MES users, roles, permissions, and access controls while monitoring performance and availability.
• Support MBR/EBR lifecycle management, process improvements, documentation, and compliant manufacturing execution.

Requirements

• Experience supporting Manufacturing Execution Systems and hands-on experience with Werum PAS-X.
• Strong experience with MES integrations, including SAP PP-PI or other ERP systems.
• Application support experience in a GxP-regulated pharmaceutical or life sciences environment.
• Knowledge of MBR/EBR lifecycle management, incident management, troubleshooting, and root cause analysis.
• Understanding of MES administration, user management, access control, and validation requirements.
• Fluent English required, with strong analytical, communication, and stakeholder collaboration skills.

Nice to have

• Experience with computerized system validation (CSV).
• Familiarity with manufacturing automation and shop-floor systems.
• Experience with CAPA, change management, and deviation processes.
• Knowledge of pharmaceutical manufacturing and packaging operations.
• Experience in Agile or global delivery environments.

Culture & Benefits

• Full-time remote work arrangement.
• Collaboration with Manufacturing, Quality, Validation, and IT stakeholders.
• Work on regulated pharmaceutical manufacturing systems and continuous process improvement.
• Exposure to fixed-price and time-and-materials delivery models.