Senior Commissioning Lead – GMP Pharma Facility

Planet Pharma; Mol; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

Planet Pharma seeks an experienced Commissioning Lead to drive end‑to‑end commissioning for a highly regulated pharmaceutical facility on a 2‑3 year consultancy assignment in Belgium.

You will coordinate planning, testing, and handover to operations, ensuring GMP compliance and managing cross‑functional teams across facilities, utilities, and control systems. Fluency in English is required and prior pharma/regulatory experience is preferred.

Qualifications

• 10-15 years of experience delivering commissioning activities in complex industrial or regulated environments.
• Strong knowledge of commissioning methodologies including IQ/OQ/PQ, FAT/SAT, testing protocols and commissioning documentation.
• Experience in GMP-regulated industries is essential.

Responsabilités

• 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 with project planning teams to ensure commissioning is integrated into the overall project schedule.
• Identify and manage dependencies between facility infrastructure, utilities, process equipment, and control systems.
• Lead integrated commissioning and cross-functional testing activities and ensure readiness before handover.
• Coordinate with equipment suppliers, third parties, and regulatory stakeholders as required.
• Maintain the commissioning register and track readiness, acceptance status, and progress.
• Support the transfer of commissioning data into maintenance and asset management systems.

Connaissances

Commissioning leadership

IQ/OQ/PQ knowledge

Regulatory compliance

Description du poste

Planet Pharma seeks an experienced Commissioning Lead to drive end‑to‑end commissioning for a highly regulated pharmaceutical facility on a 2‑3 year consultancy assignment in Belgium.

You will coordinate planning, testing, and handover to operations, ensuring GMP compliance and managing cross‑functional teams across facilities, utilities, and control systems. Fluency in English is required and prior pharma/regulatory experience is preferred.