Production Engineer

Production Engineer ------------------- Roche Schweiz bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-standing customer, Roche Diagnostics International AG in Rotkreuz, we are looking for a Production Engineer ======================= Background: Roche's Global Instrument Network (GIN) delivers reliable and innovative instruments for in-vitro diagnostics to our subsidiaries and our customers. We manufacture a wide range of instruments, from point-of-care devices to large routine laboratory instruments. Our network has five hubs, i.e., we work from five locations (Mannheim, Ludwigsburg, Tucson, Rotkreuz and Suzhou). As a network, we will work together to constantly improve manufacturing costs, strive for the timely delivery of best-quality instruments, and thus enable Roche to bring innovative and differentiated instruments to the market. With multiple locations and areas of expertise, many paths are open to our network employees to explore the world of diagnostics in their best interest. Our Production Engineering department includes over 100 talented engineers and technicians at four different locations in Europe, China and the USA. As a service department, our main focus is on the proactive design, optimization and maintenance of production processes and product designs for the GIN Network. We strive to remain at the forefront of technology and industry trends and to use our expertise to achieve operational excellence. The global Production Engineering team is part of the global Engineering Chapter and is responsible for cost-effective, reliable and lean Change Control Management (ECR). The scope of this team's tasks primarily includes product maintenance topics for established products and the introduction of new products from the pilot phase to commercial production. The sub-chapter brings technical expertise to carry out successful material, system, process and product changes. Tasks & Responsibilities: • Coordination of technical changes: responsibility for the planning, coordination, technical evaluation, task assignment and implementation of changes in consultation with the Product Leader and/or Sub-Chapter Lead. • Creation and maintenance of specification and testing documents, work plans, material master data and bills of materials. Training of the required documents and responsible for the smooth incoming and outgoing control of changes in production. • Proactive control and communication for the timely completion of ECRs. • Responsibility for compliance with quality targets, deadlines and regulatory requirements, such as responsibility for testing documents and master data for product manufacturing. • Management of smaller projects assigned by the Product Lead or Sub-Chapter Lead (e.g. continuous improvement process, harmonization projects). • Support of development projects and assistance, e.g. in the creation of samples and prototypes, coordinates the required materials and provides feedback on manufacturability. Must Haves: • Completed technical training with a technical college entrance qualification (Fachhochschulreife) as well as further training as a state-certified technician in the field of technology and automation technology. • Initial experience in the area of assembly, testing and complaint processing and repair processing of medical diagnostic devices. Practical experience in device assembly and/or as a skilled worker in electronics or as a technical expert is an advantage. • Experience in the transfer of new projects into production, as well as in the design of the production line, material management and the coordination, assembly and repair of breadboards and functional models of complex mechatronic systems in a GMP environment, preferably for regulated medical products. • Proven experience in the coordination of complex processes, change and stakeholder management with a strong service mentality and "we can do it" mentality to actively break open existing structures. • Strong team and communication skills for successful work in an international matrix organization. Due to the ION Network interfaces in Germany, Switzerland and the USA, very good German and English skills in spoken and written form are required, enabling international cooperation. • Willingness and appropriate affinity to learn new digital tools and enjoyment of working in a changing environment with appropriate flexibility and personal responsibility. • Willingness for occasional assignments in neighboring foreign countries. Nice to haves: • SAP knowledge. What is offered to you: • A chance to contribute to one of the most significant pharmaceutical companies in the world • Modern campus with lots of green spaces and meeting zones • Central location with highway access and railway station nearby • Varied activity profile • Home office possibility • Further training opportunities through temptraining • Collaboration in a dynamic and motivated team • Good remuneration You are welcome to send your complete application documents to Herr Severin Räfle. Chemie Pharma Pharmacy Diagnostik Zug Luzern Vollzeit Fulltime Forschung Laboratory