Quality Assurance Assistant - Meldola, Emilia-Romagna EUR 50.000 - 70.000 6 giorni fa Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Advanced Accelerator Applications, a Siemens Healthineers company, is a global leader in the production of PET radiotracers. With over two decades of expertise, we are committed to delivering high-quality, reliable diagnostic radiopharmaceuticals and services that have established us as a trusted partner in PET imaging. As part of Siemens Healthineers Molecular Imaging business, we are integrated into a global network of 60 radiotracer production facilities. Siemens Healthineers is the largest supplier of PET diagnostic radiopharmaceuticals, delivering approximately two million doses annually to more than 3,100 imaging centers worldwide. At Advanced Accelerator Applications, we believe in fostering an inclusive, diverse, and collaborative environment where every individual is valued. We encourage personal and professional growth, offering opportunities to step outside your comfort zone while providing the resources and flexibility to thrive. Join us to make a meaningful impact on global healthcare and be part of a team dedicated to shaping the future of medical imaging. Apply now for the position of Quality Assurance Assistant in Meldola, Forlì Cesena, and you will collaborate with the QA department for the management and review of GMP documentation and batch record to assure the respect of the GMPs and Health Authorities requirements at local level. Your role: You support the QA department, Production Manager and Quality Control Manager in managing, reviewing and archiving the site GMP documentation. You redact and review SOPs, records, protocols and reports according to GMPs, National/Corporate Guidelines and Health Authorities' requirements. You support the Quality Control Manager with the acceptance of incoming materials and the management of relative documentation. You support the QA department in the managing of training records, execution at local level of staff GMP training and redaction of the Training Annual Plan. You support the QA department in the management of not-compliance (Out of Specifications, System Sustainability Test failure, Out of Trend, Deviations), CAPA and Change Controls. You support the QPs in the batch record review. Your expertise: Pharmaceuticals, Chemical or Biological degree. Fluent knowledge of English language. Previous experience in radiopharmaceutical companies is desirable. We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. As an equal opportunity employer, we welcome applications from individuals with disabilities. J-18808-Ljbffr