Project Manager / PMO Digital Industrial Solutions

Oxford Global Resources; Cataluña; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Oxford Global Resources is seeking an experienced PMO – Digital Industrial & QA Solutions to support strategic digital transformation initiatives within a leading pharmaceutical organization. The role focuses on delivering Manufacturing, Laboratory, and Quality Systems projects, collaborating with QA, QC, Manufacturing, Engineering, and IT teams.

You will drive governance, planning, and execution, track milestones, manage risks, and ensure GxP compliance and audit readiness across complex,

Formación

• PMO, Project Coordinator, or PM experience in pharma/life sciences.
• Strong understanding of GxP-regulated environments.
• Knowledge of Manufacturing, Laboratory, or Quality Systems.
• Experience with governance, reporting, and stakeholder management.
• Excellent communication and organizational skills.

Responsabilidades

• Support governance, planning, and execution of strategic projects.
• Track project plans, milestones, deliverables, and dependencies.
• Manage risks, issues, and change requests.
• Prepare Steering Committee materials and status reports.
• Monitor KPIs, budgets, resource allocation, and progress.
• Coordinate activities with stakeholders and vendors.
• Ensure compliance with GxP requirements and audits.
• Maintain project documentation and governance standards.

Conocimientos

PMO experience

Project coordination

GxP-regulated environments

Stakeholder management

Communication skills

Organizational skills

Herramientas

PAS-X (MES)

LIMS / LES

LabWare

Descripción del empleo

PMO – Digital Industrial & QA Solutions | Pharmaceutical Industry

We are seeking an experienced PMO – Digital Industrial & QA Solutions to support strategic digital transformation initiatives within a leading pharmaceutical organization.

This role will play a key part in the successful delivery of critical Manufacturing, Laboratory, and Quality Systems projects, working cross-functionally with QA, QC, Manufacturing, Engineering, and IT teams.

Key Responsibilities

• Support governance, planning, and execution of strategic projects
• Track project plans, milestones, deliverables, and dependencies
• Manage risks, issues, and change requests
• Prepare Steering Committee materials and project status reports
• Monitor KPIs, budgets, resource allocation, and project progress
• Coordinate activities with internal stakeholders and external vendors
• Ensure compliance with GxP requirements, validation processes, and audit expectations
• Maintain project documentation and governance standards

Desired Experience

• PMO, Project Coordinator, or Project Management experience in the pharmaceutical, biotech, or life sciences industry
• Strong understanding of GxP-regulated environments
• Knowledge of Manufacturing, Laboratory, or Quality Systems
• Experience with governance, reporting, and stakeholder management
• Excellent communication and organizational skills

Preferred Systems Experience

• PAS-X (MES)
• LIMS / LES
• LabWare
• Quality and Manufacturing digital platforms

Ideal Candidate

You are a proactive and detail-oriented PMO professional who thrives in complex, regulated environments and enjoys coordinating multiple stakeholders, vendors, and technical teams to ensure successful project delivery.