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With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases. Collaborates to ensure that the site´s Quality System is maintained compliant to regulatory and GxP compliance requirements Collaborates in the management of the site´s Quality Systems Documentation and reviews. Collaborates in the Quality System Management including management of Non-Conformances, CAPAS, Change Control, Training, Effectiveness Checks. Support the Quality Team in the Authorities Inspections, Clients Inspections and Autoinspections Acts as QP for the Certification of Conformance of the product (pharma, medical devices, food and hygiene products) according to the GMP (Annex 16) and the regulation in reference of these products of the products manufactured in the plant. Bachelor´s Degree in Pharmacy or training to act as Qualified Person (according to the Spanish Royal Degree 824/2010 art.More than 5 years of experience in GxP pharma company manufacturing operations up of with more than 3 years in Quality Assurance Role Knowledge in SAP, Veeva, ESKO will be valued Fluent English and Spanish written and spoken
