Responsibilities: Set up, practical execution and troubleshooting of upstream operations in fed-batch processes under Good Manufacturing Practices (GMP) Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility Management and documentation of process execution, deviations, changes and CAPAs. Partnering with Quality Assurance and other internal stakeholders during investigations and technical discussions Involvement in continuous improvement efforts and support for the implementation of new technologies, including non-GMP engineering runs or testing activities Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing Material management using ERP systems (SAP) Mentoring and training of junior team members, active participation in knowledge transfer Participation in sampling activities or on-call duties, which may include weekend work
Our Company is a leading biopharmaceutical company employing over 1,000 people in Switzerland at three sites. The company’s headquarters are in Lucerne. At the site in Zurich, the company operates a global innovation and development hub. In addition, we manufacture medicines for global clinical trials and operate a forensic laboratory in Schachen (Canton Lucerne). We conduct around 40 clinical trials annually in Switzerland. The main therapeutic areas include oncology, infectious diseases, cardiovascular and cardiometabolic diseases. We also have a broad portfolio of vaccines for the prevention of diseases in children, adolescents, and adults and we are one of the leading companies in veterinary medicine. Furthermore, we take our responsibility to the local community seriously and have been involved for many years in initiatives such as the «Trendtage Gesundheit Luzern» and the «Alliance Health Competence».
