Global MES Project Manager - PAS-X Expert for Life Sciences

Fusion Consulting

Paris

Sur place

EUR 90 000 - 120 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Workflex – 25 days off annually
Flexible Time Off
Annual Training Budget – CHF 1,500
Unity Scheme

Résumé du poste

Fusion Consulting is seeking an experienced MES Project Manager to lead large-scale MES transformations for a leading life sciences organization. The role requires strong Koerber PAS-X expertise and proven capability to drive cross-functional teams including manufacturing, quality, validation, and IT in a regulated pharmaceutical environment.

You will oversee end-to-end project delivery, from design through deployment and go-live, ensuring compliance with GxP, CSV and industry standards while

Qualifications

  • Proven experience leading MES projects in pharma/life sciences.
  • Strong knowledge of Koerber PAS-X.
  • Experience with MES integrations with ERP/warehouse/enterprise systems.
  • Understanding of GxP and CSV fundamentals.
  • Familiarity with ISA-95 is a plus.

Responsabilités

  • Lead end-to-end MES projects from design through deployment and go-live.
  • Coordinate cross-functional teams across business, manufacturing, quality, validation, and IT.
  • Manage scope, timelines, risks, budgets, and stakeholder communications.
  • Support global MES template deployments and process harmonization.
  • Oversee system integration, testing, validation and implementation activities.
  • Ensure compliance with GxP, CSV and industry standards.

Connaissances

Project management
Stakeholder management
Cross-functional teamwork
French & English communication
MES integrations (ERP/WM/enterprise)

Outils

Koerber PAS-X

Description du poste

Fusion Consulting is seeking an experienced MES Project Manager to lead large-scale MES transformations for a leading life sciences organization. The role requires strong Koerber PAS-X expertise and proven capability to drive cross-functional teams including manufacturing, quality, validation, and IT in a regulated pharmaceutical environment.

You will oversee end-to-end project delivery, from design through deployment and go-live, ensuring compliance with GxP, CSV and industry standards while

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