Universität Basel: Member of the Quality Assurance Team at the GMP Facility for Advanced Therapies (80-90%) Member of the Quality Assurance Team at the GMP Facility for Advanced Therapies (80-90%) As a joint venture of the University of Basel and the University Hospitals Basel, the Department of Biomedicine (DBM) brings together basic and clinical scientists to advance the understanding of health and disease. We are home to more than 67 research groups and over 800 employees across six locations in the heart of Basel. Our collaborative and international environment fosters innovation, excellence, and impactful research. The Core Facilities GMP led by Anke Wixmerten, is looking for a Member of the Quality Assurance Team (80-90%). Join our community and help shape the future of biomedicine.   Your position The state-of-the-art facilities on the USB campus provide all DBM researchers with access to a fully GMP-compliant environment for ATMP manufacturing and regulatory support for translational research projects and clinical trials. The GMP Facility for Advanced Therapies comprises two production sites and a core team of five people. A new facility together with the ETH Zürich is located at the Department of Biosystems Science and Engineering (DBSSE). Responsibilities include Assisting the transfer of processes from the DBM to the facility at the DBSSE Supplier qualification and audits of material suppliers and service providers as well as material management Assisting the core facility team and users with GMP-compliant documentation Assisting users with the implementation of their projects (from research to GMP) Participating in inspections by regulatory authorities and other audits Validation of Quality Control Assays (FACS) Your profile The successful candidate should meet the following requirements Experience in the GMP-compliant manufacturing of (preferably) ATMPs in a cleanroom facility (GMP) according to PIC/S and Swiss legislation Excellent command of English (spoken and written), German is an asset University degree in natural sciences (preferably biology) Regulatory experience in a GMP environment High level of reliability and a strong sense of responsibility  Excellent interpersonal and communication skills Self-motivated and able to work both independently and as part of a team   We offer you Opportunities to contribute to a wide range of projects focused on translating innovative ATMPs into clinical trials Engaging work in a dynamic and international research environment Attractive working conditions and salary in line with the standards of the University of Basel Application / Contact Please submit your application, including your resume, a description of your relevant experience, and contact information for references. The position is available immediately or by agreement. For informal inquiries, please contact Anke Wixmerten ( [email protected] ).  Apply www.unibas.ch