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CAPEX Project Manager

  1. Brussels
  1. Contract
Competitive
24864/ZM
  1. CAPEX Projects
Date Posted22 May 2020
Capex Project Manager - Global Pharmaceutical Organisation - Belgium

We have an exciting opportunity for an experienced Capex Project Manager to join a large new project for a global pharmaceutical organisation, in Belgium with great longevity of employment possibility.

DUE TO TRAVEL RESTRICTIONS CAUSED BY THE CORONAVIRUS WE CAN ONLY ACCEPT APPLICATIONS FROM THOSE RESIDING IN The UK AT THIS TIME.

Who are we looking for?
  • Responsible for delivery of project goals in terms of cost, time, functionality and according to client expectations.
  • Responsible for the maintenance of quality systems and cGMP compliance for the business by ensuring that all project managers and teams comply with processes, procedures and instructions for all activities in which the team participates.
  • Establish project charter including scope of work, goals and deliverables together with the relevant project champion to support business objectives in collaboration with senior management and stakeholders.
  • Clarifying roles and responsibilities within the project organization and developing full-scale project plans and associated communication documents.
  • Securing optimal flow of information within project organization and at interfaces with project champion/project steering committee as well as any other relevant stakeholders within either the wider CGT/BS SGIE team and/or the wider Tech Ops community.
  • Reporting regularly in writing, including project progress reports. Includes both internal to Lonza stakeholders as well as EPC stakeholders  
  • Identifying and recommending the internal and / or external resources to reach the project goals and managing day-to-day operational aspects of projects.
  • Identifying and managing project dependencies and mapping the critical path.
  • Establishing the project team/ structure necessary to reach the project goals and ensures appropriate coaching/development/performance feedback to all direct reports in order to develop a strong and competent team.
  • Ensuring compliance with all pertinent safety policies, rules and regulations
The ideal candidate will have:
  • Experience of leading sterile filling projects/Biotech experience
  • Experience of design, construction
  • CQV and handover within a bio environment
  • Stakeholder management in a project matrix organization
  • Regular reporting to stakeholders
For more information on this project / position, please apply with a copy of your up to date CV today!      



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