Senior Project Manager - Remoto

Adroit People Limited (UK); Madrid; A distancia; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A leading recruitment agency is seeking an experienced Senior Project Manager to lead and deliver complex MES programs within the Pharmaceutical Manufacturing division. The ideal candidate will have over 7 years of project management experience, ensuring compliance with GxP and validation practices while managing global, cross-functional teams. This role offers the opportunity to work in a dynamic and regulated environment, supporting operational excellence and product quality.

Formación

• Minimum 7+ years of experience in project management focusing on Pharma Manufacturing IT systems or MES.
• Strong understanding of GxP, CSV, 21 CFR Part 11, and data integrity principles.
• Excellent understanding of pharmaceutical production processes.

Responsabilidades

• Lead end-to-end delivery of MES programs from initiation to deployment.
• Define project scope, timelines, and deliverables collaboratively.
• Drive governance and track project progress against milestones.

Conocimientos

Project Management

MES expertise

GxP knowledge

Stakeholder Management

Regulatory Compliance

Cross-functional project management

Educación

Project Management certifications (PMP, PRINCE2, or Agile PM)

Descripción del empleo

Role :

Job Title : Senior Project Manager – Pharma Manufacturing (MES / PharmaSuite)

Location : Poland / Spain (Remote)

Permanent Full Time Employment

We are seeking an accomplished Senior Project Manager to lead and deliver complex, large-scale Manufacturing Execution Systems (MES) programs within our Pharmaceutical Manufacturing division. This role requires a unique combination of technical expertise, strategic leadership, and regulatory awareness to drive initiatives that directly support operational excellence, product quality, and compliance in a GxP-regulated environment.

The ideal candidate will possess deep domain experience in MES, particularly with Rockwell Automation’s PharmaSuite platform, and a demonstrated ability to manage multi-site, cross-functional projects in alignment with stringent validation and compliance standards.

Project Leadership & Delivery

Lead the end-to-end delivery of MES programs from initiation through deployment, validation, and hypercare.

Define project scope, timelines, and deliverables in collaboration with stakeholders from IT, manufacturing, quality, and automation.

Drive governance, track progress against milestones, and ensure projects are delivered on time, within scope, and on budget.

Collaborate with engineering and manufacturing teams to define and optimize business processes supported by MES.

Ensure all system changes comply with Computer System Validation (CSV), GxP, and data integrity standards.

Stakeholder Management & Communication

Serve as the primary liaison between business sponsors, global delivery teams, and third-party vendors.

Conduct regular status reviews, steering committee presentations, and project health assessments.

Foster collaboration and alignment across global sites to ensure consistent delivery practices.

Quality, Compliance & Continuous Improvement

Champion quality-by-design and validation best practices throughout the system lifecycle.

Stay current with evolving regulatory requirements, industry trends, and MES technologies to influence roadmap planning.

Min 7+ years of proven experience in project management with a focus on Pharma Manufacturing IT systems or MES implementations.

Strong understanding of GxP, CSV (Computer System Validation), 21 CFR Part 11, and data integrity principles.

Excellent understanding of pharmaceutical production processes, batch management, and shop floor systems integration.

Proven experience managing global projects with distributed teams and multiple stakeholders.

Project Management certifications such as PMP, PRINCE2, or Agile PM are preferred.

Prior experience working with leading pharma or biotech organizations will be a strong advantage.