Batch release & certification of APIs, excipients, primary packaging, bulk products (tablets & injectables), and final packaged products. * Managing deviations, investigations, CAPAs, recalls, change controls, retests, rework/reprocess, and approval of PQRs/LQRs. * Reviewing and approving procedures in the QP activity scope. * Supporting internal audits, client audits, and inspections. * Ensuring products meet GMP standards and regulatory/MA dossier requirements. * Belgian Qualified Person (QP) number – mandatory and non‑negotiable * Operational mindset: enjoys being on the shopfloor and reacting swiftly to production realities. * Strong French communication skills (native or fully fluent) + good English for interactions with global teams. * Ability to work under pressure and remain supportive yet firm, especially when blocking non‑compliant batches.
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