MES Integration Specialist (Werum PAS-X)

TL;DR

MES Integration Specialist (Werum PAS-X) (MES/Werum PAS-X): Supporting and enhancing manufacturing execution operations in a regulated pharmaceutical environment with an accent on Level 2 support, MES-to-ERP integrations, and compliant production execution. Focus on troubleshooting interface failures, managing MBR/EBR lifecycles, resolving complex incidents, and maintaining reliable GxP-validated systems.

Location: Full remote from Poland; Warsaw is listed as the location.

Company

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

What you will do

• Provide Level 2 support for MES applications used in manufacturing and packaging operations.
• Troubleshoot incidents, execution issues, interface failures, and production support requests.
• Perform root cause analysis and coordinate resolution with L3 teams, vendors, and business stakeholders.
• Support and maintain integrations between Werum PAS-X, SAP PP-PI, ERP, and other manufacturing systems.
• Administer users, roles, permissions, and access controls while monitoring system reliability and availability.
• Support MBR/EBR lifecycle management, system enhancements, documentation, and GxP-compliant validation activities.

Requirements

• Hands-on experience supporting MES applications and working 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, and access control.
• Fluent English and availability to work remotely from Poland are required.

Nice to have

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

Culture & Benefits

• Full-time remote work arrangement from Poland.
• Collaboration with Manufacturing, Quality, Validation, IT, vendors, and business stakeholders.
• Work across regulated pharmaceutical manufacturing and packaging operations.
• Opportunity to contribute to process improvements, system enhancements, and documentation.