QP certification of biological drug substance, drug product and finished drug product in compliance with Marketing Authorisations, GMP and EU/ROW market’s national requirements Review and disposition of external manufactured Drug Substance, Drug Product and QP certification of Finished Drug Product to products’ authorisations and GMP This team is responsible for biological material disposition, including QP certification, of material manufactured at contract manufacturing organisations on behalf of Takeda This individual will work in the Disposition Team of the External Biologics Quality Organization at Takeda and will be based in Dublin. I further attest that all information I submit in my employment application is true to the best of my knowledge.
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