QA/QC Manager

Our client is Europe’s leading provider of construction solutions, delivering complex engineering and construction projects for the world’s leading corporations across sectors including enterprise and hyperscale data centres, advanced technology and life sciences, and fire protection - powered by innovative people and a supportive culture that helps everyone reach their full potential.

Overview

Lead on-site QA/QC to ensure construction activities meet approved drawings/specifications and GMP / EU GMP expectations, and support delivery of an audit‑ready regulated facility in Belgium/EU through to handover.

 Key Responsibilities

• Own and deliver the project/site Quality Plan and QA/QC processes for a regulated (pharma) construction project
• Ensure works comply with project quality requirements, contract requirements, and approved drawings/specifications (ISO 9001 expectations as applicable)
• Plan/lead inspections, ITP execution, and punch list/walkdown closeout to achieve right-first-time delivery
• Manage NCRs/deviations and drive CAPA/root-cause investigations to closure; escalate quality risks and trends
•  Lead quality audits (internal, subcontractor/vendor) and support client and regulatory readiness audits for GMP / EU GMP regulated facilities (Belgium/EU)
• Maintain audit-ready documentation and ensure dossiers/test packs are complete for handover
• Interface with CQV / Validation teams to align inspection/testing evidence, turnover dossiers, and handover readiness (as-built, test packs, certifications, and traceability)
• Act as the quality interface across construction, subcontractors, suppliers, and client teams; provide training/briefings as needed

Critical Requirements

• Proven QA/QC management experience on pharmaceutical/life-sciences construction projects (or similarly regulated environment)
• Strong knowledge of construction quality control, inspection/testing, and turnover/handover documentation (test packs/dossiers)
• Working knowledge of GMP / EU GMP expectations as they apply to construction, documentation, and turnover in regulated facilities
• Experience supporting CQV / Validation (commissioning, qualification, and validation) interfaces, documentation, and handover deliverables
• Demonstrated experience managing NCRs/deviations, CAPA and root-cause investigations
• Ability to lead audits and manage subcontractor/vendor quality performance
• Strong stakeholder management and communication skills; able to work to schedule pressure and strict deadlines
• Relevant degree or professional qualification

 Location – Belgium (Site Based)

Contract Duration – 18 Months