1 час назад
MES Integration Specialist (Werum PAS-X)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
MES Integration Specialist (Werum PAS-X) (Pharmaceutical Manufacturing): Supporting and enhancing MES operations in a regulated pharmaceutical manufacturing environment with an accent on Level 2 support, ERP integrations, and MBR/EBR lifecycle management. Focus on troubleshooting production incidents, performing root cause analysis, maintaining reliable MES interfaces, and ensuring GxP and validation compliance.
Location: Full remote, based in Warsaw, Poland
Company
is an IT consultancy firm delivering software solutions and technology services to startups, mid-sized companies, and large corporations across multiple industries.
What you will do
- Provide Level 2 support for MES applications used in 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 MES, SAP PP-PI, ERP, and other manufacturing systems.
- Administer MES user accounts, roles, permissions, and access controls while monitoring system performance and availability.
- Support MBR/EBR lifecycle management, system enhancements, documentation, and compliant manufacturing process execution.
Requirements
- Experience supporting Manufacturing Execution Systems and hands-on experience with Werum PAS-X.
- Strong, mandatory 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.
- Strong analytical, problem-solving, communication, and stakeholder collaboration skills; fluent English.
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 position with a remote work arrangement.
- Work on technology solutions for pharmaceutical, life sciences, manufacturing, and other enterprise industries.
- Collaboration with Manufacturing, Quality, Validation, IT, vendor, and business stakeholder teams.
- Focus on compliant, reliable, and continuously improving manufacturing operations.
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