Manufacturing Line Specialist - Anlagemeister 80%-100% (m/f/d)

The actual location of this position is in Visp, Switzerland. Relocation support is available to eligible applicants and their families if required. Become part of our team in Visp and help ensure reliable and efficient plant operation in a highly regulated biopharmaceutical environment. In this varied role, you will support production campaigns, drive technical improvements, and make a direct contribution to the manufacturing of innovative therapies. What awaits you: An agile career and a dynamic work culture. An inclusive and ethical work environment. Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous benefits for lifestyle, family, and leisure. Our full list of local benefits can be found here: Benefits in Visp: https://bit.ly/3wjkoFi Your tasks: Supervision of pilot and production campaigns as well as ensuring plant operation and technical support, including outside regular working hours as part of on-call service. Creation, maintenance, and optimization of cGMP-compliant documentation such as SOPs, HSPs, and checklists in close cooperation with MSAT and the process biotechnologists. Ensuring that technical and operational requirements are taken into account as early as the planning and engineering phase of projects. Coordination and support of engineering, workshop, and technical teams for investments, plant preparations, and technical improvements. Monitoring production activities as well as ensuring compliance with planned work and initiating corrective measures in the event of deviations. Co-responsibility for the technical instruction and training of employees as well as supporting teams with plant-related technical questions. Continuous improvement of plants, processes, and workflows according to Lean, Kaizen, and 6S principles while complying with safety, quality, hygiene, and environmental standards. What we are looking for: Completed training as a chemical and pharmaceutical technologist, chemical and biological laboratory technician, or a university degree (Bachelor/Master) in biotechnology, pharmaceutical sciences, or a related field. Several years of experience in a GMP-regulated production environment or in a comparable pharmaceutical or biotechnological function. Sound knowledge of process plants and automation systems, especially DeltaV. Strong technical understanding as well as the ability to approach technical challenges in a structured and solution-oriented manner. Experience in creating and maintaining GMP-relevant documentation as well as working with cross-functional teams. Very good German skills in spoken and written form. Commitment to continuous improvement as well as high standards in the areas of safety, quality, and compliance. About Lonza: At Lonza, our employees are our greatest strength. At over 30 locations on five continents, our globally networked teams work together every day to manufacture the medicines of tomorrow. Our core values: collaboration, accountability, excellence, passion, and integrity reflect who we are and how we work together. The ideas of each individual, whether big or small, have the potential to improve millions of lives, and that is exactly what we want you to be a part of. Innovation thrives when people of diverse backgrounds bring their unique perspectives. At Lonza, we value diversity and are committed to an inclusive environment for all employees. If you are ready to turn our customers' groundbreaking ideas into actionable therapies, we look forward to welcoming you on board. Ready to shape the future of Life Sciences? Apply now.