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MES Integration Specialist (Werum PAS-X)

Формат работы
remote (только Poland)
Тип работы
fulltime
Английский
c1
Страна
Poland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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