Description
The Quality Systems Specialist will support pharmaceutical quality systems by writing and monitoring test protocols, reports, change requests, CAPAs, root cause analyses, URSs, and technical procedures; managing test, change, and CAPA action lists; supporting audits, risk assessments, and technical assessments; and ensuring GMP compliance and documentation during production. The role requires a technical bachelor's degree or equivalent experience, pharmaceutical-sector experience, GMP knowledge, MS Office, and Dutch and English proficiency, and is offered as a permanent, full-time day-shift position with benefits.
