Description
The QA Qualification Engineer will support the qualification, risk management, documentation review, lifecycle management, deviation and CAPA handling, audit readiness, and stakeholder coordination of advanced process and laboratory equipment, utilities, and sterile production areas in a regulated pharmaceutical environment. The role requires at least five years of relevant quality experience, extensive qualification and risk-based methodology experience, strong communication skills, and fluent Dutch and English. It is based in Beerse with a hybrid arrangement of three on-site days and two remote days, and offers both permanent and freelance-consultant employment options.
