Quality Specialist, Quality Assurance

Quality Specialist, Quality Assurance page is loaded Quality Specialist, Quality Assurance Apply locations Modena time type Full time posted on Posted 3 Days Ago job requisition id JOB ID-08694 Evotec is a life science company with a unique business model that delivers on its mission to discover and develop highly effective therapeutics and make them available to the patients. The Company’s multimodality platform comprises a unique combination of innovative technologies, data and science for the discovery, development, and production of first-in-class and best-in-class pharmaceutical products. Evotec leverages this “Data-driven R&D Autobahn to Cures” for proprietary projects and within a network of partners including all Top 20 Pharma and over 800 biotechnology companies, academic institutions, as well as other healthcare stakeholders. Evotec has strategic activities in a broad range of currently underserved therapeutic areas, including e.g. neurology, oncology, as well as metabolic and infectious diseases. Within these areas of expertise, Evotec aims to create the world-leading co-owned pipeline for innovative therapeutics and has to-date established a portfolio of more than 200 proprietary and co-owned R&D projects from early discovery to clinical development. Evotec operates globally with more than 4,200 highly qualified people. The Company’s 16 sites offer highly synergistic technologies and services and operate as complementary clusters of excellence. For additional information please go to www.evotec.com and follow us on Twitter Evotec and LinkedIn . We have an interesting opportunity at Evotec Modena, Medolla (MO) for a GMP Quality Assurance, possibly experienced in aseptic manufacturing . This position will have a key role in Cell and Gene therapy team to guarantee company and intercompany ATMP manufacturing activities . Essential Functions manage a comprehensive documentation system for all Cell Factory operations collaborating in risk analysis collaborating in change management system managing deviations and corrective/preventive actions regularly inspect all departments and assess their GMP compliance status support the development of appropriate training plans for new and existing staff qualify external suppliers handling complaints distributing production batch records execute the Batch Record Review Required Skills & Abilities Knowledge of current GxP guidelines Positive, team player and problem-solving attitude Accurate, with excellent prioritization and organization skills Commitment to the assigned deadlines and ability to deliver them tightly English intermediate level is required (written and spoken) Good knowledge of Microsoft Office applications Education BS or MS Scientific Degree (e.g. Biotechnology, Biology, Pharmacy, CTF…) Experience Previous experience in Quality Assurance is mandatory (2 years) Previous experience with ATMPs is a plus Previous experience with sterile products is a plus FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap. ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities. Similar Jobs (1) QC Manager in ATMP locations Modena time type Full time posted on Posted 30 Days Ago About Us Evotec is a life science company with a unique business model focused on delivering highly effective new therapeutics to the patients. The Company leverages its multimodality platform, the “Data-driven R&D Autobahn to Cures”, for proprietary projects and within a network of partners including Pharma, Biotech, academics, and other healthcare stakeholders. With more than 4,500 highly qualified people at 17 sites, Evotec aims to create the world-leading co-owned pipeline for innovative therapeutics. For additional information please go to www.evotec.com and follow us on Twitter Evotec and LinkedIn . Please click on the link below to access and review our Privacy Information for Applicants: Privacy Information for Applicants J-18808-Ljbffr