IT project manager in pharma

Fusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry, partnering with leading companies in pharma, healthcare, and animal health. We are looking for a Senior IT Project Manager to lead a global eQMS consolidation and transformation program, bringing the current quality management landscape from five different platforms into a single harmonized solution.

• Lead the global eQMS consolidation program, transitioning from multiple existing quality management systems toward a single harmonized Veeva-based platform.
• Drive adoption of the Vacaville Veeva platform as the foundation for the future One Lonza eQMS landscape.
• Manage the program roadmap across three main phases: Technical Readiness, Scale and Enhance.
• Coordinate cross-functional activities across Quality, IT, business, technical teams, vendors, and individual sites.
• Manage project plans, timelines, milestones, dependencies, risks, issues, and decision-making across multiple workstreams.
• Support harmonization of quality processes and workflows across different sites while balancing global standards with site-specific needs.
• Drive technical and organizational readiness for multi-site implementation and deployment.
• Coordinate system integrations and dependencies required for the new eQMS landscape.
• Manage migration and transition activities from legacy systems including TrackWise, SciLife, MasterControl, and Lotus Notes.
• Ensure effective stakeholder communication and alignment across global and local teams.
• Improve visibility and collaboration for internal stakeholders and customers through standardized processes and a consolidated quality management platform.
• Support the long-term scalability and future readiness of the global eQMS solution.

• Proven experience managing Quality Systems (eQMS) projects end-to-end within pharmaceutical GxP-regulated environments.
• Strong hands-on IT Project Management experience covering requirements gathering, workshops, testing, deployment, hypercare, and vendor coordination.
• Pharmaceutical industry experience is a must.
• Solid understanding of Quality processes, including Deviations, CAPAs, Change Controls, Investigations, Audit Management, and Supplier Quality.
• Experience with CSV (Computer System Validation).
• Successful delivery of global SaaS application implementations, upgrades, consolidations, and multi-site rollouts.
• Strong stakeholder management skills across Quality, QA, Regulatory, Compliance, Validation, and IT organizations.
• Experience managing third-party vendors and system integrators.
• Strong delivery mindset and ability to drive projects to completion.
• Fluent English is a must.
• Candidates must be based in Europe and have the legal right to work in their country of residence.

• We provide a competitive salary, along with an outstanding work environment that fosters long-term career development opportunities.