Senior Project Manager (remote)

Adroit People Limited (UK); Madrid; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading specialist recruitment company is seeking a Senior Project Manager to oversee complex MES programs in the pharmaceutical manufacturing sector. The ideal candidate will have over 7 years of project management experience, particularly with MES systems, and a solid understanding of regulatory compliance and quality standards. This position offers a permanent full-time role, largely remote with flexible location options across Spain and Poland.

Formación

• Min 7+ years of proven experience in project management in Pharma Manufacturing IT systems or MES.
• Strong understanding of GxP, CSV, and data integrity principles.
• Project Management certifications such as PMP, PRINCE2, or Agile PM are preferred.

Responsabilidades

• Lead the end-to-end delivery of MES programs.
• Drive governance and ensure projects are delivered on time and within scope.
• Serve as the primary liaison between business sponsors and global teams.

Conocimientos

MES expertise

Project Management

Stakeholder management

Regulatory compliance

Cross-functional collaboration

Herramientas

PharmaSuite

Rockwell Automation

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.