Manufacturing Line Specialist - Anlagemeister

Support piloting and production campaigns and ensure plant operation and technical support, including outside regular working hours as part of the on-call service. Create, maintain and optimize cGMP-compliant documentation such as SOPs, HSPs and checklists in close collaboration with MSAT and operational biotechnologists. Ensure that technical and operational requirements are considered early in the planning and engineering phases of projects. Coordinate and support engineering, workshop and technical teams during investments, plant preparation activities and technical improvement initiatives. Monitor production activities, ensure adherence to planned work and initiate corrective actions in the event of deviations. Contribute to the technical instruction and training of employees and support teams with plant-related technical questions. Continuously improve equipment, processes and workflows according to Lean, Kaizen and 6S principles while complying with safety, quality, hygiene and environmental standards.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Completed vocational training as a chemical and pharmaceutical technologist, chemical or biological laboratory technician, or a university degree at bachelor's or master's level 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 equipment and automation systems, in particular DeltaV/MES

• Strong technical understanding and the ability to approach technical challenges in a structured and solution-oriented manner

• Experience in creating and maintaining GMP-relevant documentation and working with cross-functional teams

• Very good written and spoken German skills; English skills are desirable

• Commitment to continuous improvement and a strong awareness of quality, safety, hygiene and environmental standards