Senior Quality Assurance Consultant

Senior QA Consultant – Batch Release & Audit Readiness (Randstad area)An international biopharmaceutical company in the Randstad area is looking for a Senior QA Consultant to support GMP compliance, batch release, and audit preparation activities within a fast-paced manufacturing environment.Key responsibilities:Ensure products meet GMP standards and are ready for timely QP release.Support audit and inspection readiness, including internal and external audits.Review and approve GMP documentation (deviations, CAPAs, change controls, SOPs).Collaborate with cross-functional teams to maintain quality oversight on manufacturing operations.Drive continuous improvement initiatives in QA systems and processes.Requirements:BSc or MSc in Life Sciences or equivalent.Minimum 6+ years of experience in pharmaceutical QA within GMP manufacturing.Strong understanding of EU GMP, batch release processes, and audit preparation.Proactive, detail-oriented, and comfortable working in a dynamic, matrix environment.Fluent in English; Dutch is an advantage.Contract details:Location: Randstad area (hybrid possible)Start date: ASAPDuration: 6 month Freelance PositionIf you’re an experienced QA professional with a strong background in GMP compliance and batch release, this is an excellent opportunity to join a high-performing quality organization supporting global manufacturing operations.