Ensure systems are tested and verified under representative operating conditions prior to handover.
Coordinate activities involving equipment suppliers, qualified third parties, and regulatory stakeholders where required.
Manage change control processes throughout the commissioning lifecycle, ensuring all changes are appropriately documented and implemented.
Commissioning Governance
Maintain the commissioning register and track system readiness, acceptance status, and progress.
Ensure readiness criteria and stage-gate requirements are met before systems advance to integrated testing.
Identify, escalate, and help resolve project risks and commissioning blockers.
Support the development and review of FAT and SAT protocols as required.
Operational Handover
Serve as the primary interface between project and operations teams during commissioning and startup activities.
Ensure all commissioning records and documentation are complete, traceable, and inspection-ready.
Support the transfer of commissioning data into maintenance and asset management systems.
Facilitate a structured and documented handover of systems to operations teams.
Promote early operational involvement to ensure a seamless transition to routine operation.
Safety Leadership
Provide daily oversight of commissioning activities involving live systems.
Review and challenge method statements and work permits associated with commissioning and construction activities.
Manage lockout/tagout (LOTO) processes where applicable to ensure the safe isolation and protection of systems.
About You
10-15 years of experience delivering commissioning activities within complex industrial or regulated project environments.
Proven experience leading or playing a senior role within commissioning teams on major facility, infrastructure, or process projects.
Strong knowledge of commissioning methodologies, including IQ/OQ/PQ, FAT/SAT, testing protocols, and commissioning documentation.
Broad technical understanding across facilities, utilities, HVAC, electrical, automation, process, and control systems.
Experienced in managing cross-functional stakeholders and multi-contractor environments.
Comfortable making critical decisions, enforcing readiness criteria, and escalating issues when necessary.
Experience within GMP-regulated industries is essential.
Experience in nuclear, radiopharmaceutical, or highly regulated environments would be advantageous.
Fluent English communication skills; additional European languages are considered beneficial.
Personal Attributes
Highly organised, structured, and detail-oriented.
Pragmatic and solutions-focused with the ability to maintain project momentum.
Strong collaborator who excels at bringing teams together around common objectives.
Comfortable working within evolving project environments where priorities may shift.
Motivated by delivering technically complex projects that contribute to improving patient outcomes and advancing healthcare innovation.
Contract Type: Consultancy/Freelance
Duration: 2-3 years
Location: Belgium (site-based)
Industry: Advanced Pharmaceutical / Life Sciences Manufacturing Facility
If you are interested in leading the commissioning of a technically challenging, high-impact facility project, we would be keen to hear from you.
