Ph3Location /h3 pSwitzerland, Visp /p h3What You Will Do /h3 ul liExecute manual visual inspection /li liExecutes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution. /li liProvides front line technical and procedural support, working with the manufacturing team. /li liSecuring each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements /li liResponsible for establishing timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area. /li liSupports process related investigations and assists in decision making on production issues /li liSupports process changes and CAPAs related to processes within required timelines /li liPerforms training activities of relevant areas as operator and supports others and new joiners. /li liOperating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (e.g.:compounding, parts washing, autoclaving, filter integrity testing, visual inspection) /li /ul h3What We Are Looking For /h3 ul li2-4 years of experience GMP environment on the shopfloor (preferably in sterile manufacturing of Drug Product) /li liFluent in either English or German (preferably both) /li liFamiliarity with GMP requirements, quality procedures and SOP execution /li liStrong team orientation /li liEffective communication skills and interaction with a variety of interfaces within the organization /li liStructured, focused, and well-organized working attitude /li liHigh motivation and dynamic drive /li liIT knowledge and knowledge in SAP and MES is a benefit /li liPrepared to work in 2 shifts pattern /li /ul pReference: R76558 /p /p #J-18808-Ljbffr