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Overall Quality Responsibilities
Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS DepartmentThe Qualified Person is responsible for certifying investigational medicinal products in accordance with requirements of Protocol, Investigational Medicinal Product Dossier (IMPD) and Product specification File (PSF)The compliance of all certified batches to EU Directives, Annex 16 and Annex 13 / Detailed Commission Guidelines where applicable for Investigational Medicinal Products (IMPs).Provide the Quality management team direct support and guidance in a...