GMP Project Manager — Pharma Production & Facilities

ALK; Madrid; Presencial; EUR 70.000 - 100.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Subsidized meals

Pension plan

Descripción de la vacante

ALK is seeking a Project Manager to lead pharmaceutical production, utilities, and facilities projects in Madrid. The role is hands-on, cross-functional, and focused on scope, cost, and schedules while upholding GMP and compliance.

You will coordinate with internal teams and external vendors through scoping, design, installation, qualification, and handover. The candidate should have a science or engineering degree, GMP experience, and strong English and Spanish writing and communication skills.

Formación

• Degree in Science or Engineering required.
• Experience in GMP pharmaceutical/biotech environments preferred.
• Knowledge of Quality Systems and Validation standards, policies and procedures.
• Fluent in Spanish and English; strong technical writing and communication skills.

Responsabilidades

• Lead projects across production, utilities and facilities, ensuring on-time, on-budget delivery with quality and compliance.
• Define equipment requirements and specifications based on process, safety, quality, and customer needs; set automation requirements.
• Evaluate technology to support project requirements and improvements.
• Assist in budgeting and cost management to deliver projects within approved scopes.
• Manage subcontractors and vendors to align priorities and schedules; ensure successful execution.
• Ensure quality and compliance through risk analyses, documentation, SOPs, inspections, and governance.

Conocimientos

Project leadership

Stakeholder management

GMP compliance

Technical writing

Planning & organization

Problem solving

Educación

Degree in Science or Engineering

Descripción del empleo

ALK is seeking a Project Manager to lead pharmaceutical production, utilities, and facilities projects in Madrid. The role is hands-on, cross-functional, and focused on scope, cost, and schedules while upholding GMP and compliance.

You will coordinate with internal teams and external vendors through scoping, design, installation, qualification, and handover. The candidate should have a science or engineering degree, GMP experience, and strong English and Spanish writing and communication skills.