QA specialist validating GMP systems for biologics manufacturing expansion project.
Support a pharmaceutical biologics facility expansion by overseeing equipment qualification, validation protocols, and GMP compliance documentation. The role involves reviewing technical records, managing change controls, and ensuring regulatory alignment with EU GMP and FDA standards. Ideal for an experienced validation professional who can work independently in a project-driven environment and communicate across technical and operational teams. Requires 15–20 years of pharma/biopharm manufacturing experience and fluent German and English.
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Found at a specialist agency · listed 25 August 2026 · InsideJobs links you to the original posting.