Commissioning Lead

Commissioning Lead

Location: Mol, Antwerpen Province

Category: Manufacturing

Salary: Apply for details

Country: Belgium

Employment: Contract

Worksite: On-Site

Job Description

Commissioning Lead (Contract/Freelance) | 2-3 Year Assignment

We are seeking an experienced Commissioning Lead to support the delivery of a highly regulated industrial facility. This is a long-term consultancy/freelance opportunity (2-3 years) for a professional with a strong background in commissioning complex engineering projects within pharmaceutical, nuclear, biotech, or similarly regulated environments.

The Opportunity

As the Commissioning Lead, you will be responsible for the end-to-end coordination and execution of the commissioning phase across building, process, and utility systems. You will ensure the safe, compliant, and efficient integration and handover of systems to operations, while maintaining alignment with GMP and applicable regulatory requirements.

Key Responsibilities

• Commissioning Planning & Sequencing

• Develop, own, and maintain the master commissioning strategy and sequence across all systems and workstreams.

• Define commissioning milestones, integrated testing activities, and handover gates.

• Collaborate closely with project planning teams to ensure commissioning activities are fully integrated into the overall project schedule.

• Identify and manage dependencies between facility infrastructure, utilities, process equipment, and control systems.

• System Integration & Testing

• Lead the planning and execution of integrated commissioning and cross-functional testing activities.

• 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.

• Equal Opportunity Employer

• We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

• Fraud Alert

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