Our client is a leading provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. They are a global contract development and manufacturing company for biopharmaceuticals; they provide their clients with a world-leading open access technology platform. They enable their clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing.
Due to an internal promotion, they are currently seeking to fill a critical role within the QA department. The QA Drug Substance Manufacture Lead will lead the QA team on site in Louth. Responsible for ensuring that biologic drug substance manufacturing is performed in compliance to cGMP, site SOPs and controlled documents from end-to-end, covering warehouse and supply chain management operations, manufacturing operations, batch certification by QP, batch release and shipment for biologics drug substance manufactured in their Biologics facility in Ireland.You will be reporting to the Senior Director of Quality who is also based in Ireland.
As they extend their global reach, they require someone who is interested in change, in challenge, and in building a new future together.
Role/Responsibilities