CareerPlan

Lab supervisor

Meise, BelgiumFull-time2026-10-26 → 2026-11-09

Core

Lead the QC laboratory in Meise, ensuring accurate and timely analysis of gases and raw materials according to GMP and quality management systems.

Role type

Laboratory Supervisor (Quality Control)

Builds

Certificates of Analysis, validated analytical methods, and compliant quality documentation for industrial gases and pharmaceutical intermediates.

Domain

Industrial gases / Pharmaceutical Quality Control (GMP)

Required skills

Laboratory analysis, GMP compliance, Quality Management System (QMS) management, Equipment calibration and maintenance, Team leadership and training, Document control (SOPs, OOS), Internal auditing

Preferred skills

SAP and batch information systems, Method validation, Measurement System Analysis, Statistical Quality Control, European Pharmacopoeia knowledge, Lead auditor experience

Technologies

SAP, Microsoft Office, GMP QMS software

Responsibilities

Plan and coordinate daily QC work including analyses and equipment checks; Oversee testing of raw materials, packaging, and finished products; Develop and validate analytical methods with the Qualified Person; Manage equipment qualification and documentation; Lead and train laboratory staff; Approve QC documents and act as internal lead auditor; Collaborate with Quality, Sales, and European QC teams.

Seniority

Mid-level, hands-on IC with team leadership