Manufacturing Specialist (m/w/d)

The location of this position is in Visp, Switzerland. If required, relocation support is available for eligible candidates and their families. This is an onsite position. Personal collaboration on-site enables close, direct coordination as well as the technical precision required to manufacture medicines according to the highest quality and safety standards. What we offer you: An agile career and a dynamic work culture; An inclusive and ethical workplace; Compensation programs that recognize high performance. In addition to a competitive salary, you can expect numerous benefits for lifestyle, family, and leisure. The full list of our locally tailored benefits can be found below. Benefits in Visp: https://bit.ly/3wjkoFi Your tasks: Performing manufacturing activities in accordance with cGMP guidelines in the area of buffer and media preparation for manufacturing with mammalian cells, including operating small part washing systems and autoclaves. Ensuring batch execution, evaluating test results, problem-solving, troubleshooting production equipment, and recommending solutions. Supporting the creation of SHE (Safety, Health, Environment), EM (Environmental Monitoring), operational, and cleaning risk assessments for the assigned products, as well as implementing and monitoring defined measures. Participating in document creation (e.g., electronic batch records, SOPs) for the assigned production area. Reviewing production documentation as well as processing deviations, change requests, and implementing CAPAs to ensure high GMP standards. Participating in investment projects for the construction and commissioning of new production facilities as a production expert. Responsibility for providing all necessary inputs for the setup, commissioning, and qualification of production areas and facilities. Responsibility for training production personnel on specific equipment or standard processes. Your requirement profile: Completed chemical or biopharmaceutical training or equivalent qualification; Bachelor's/Master's degree or equivalent experience in biotechnology, biology, bioprocess engineering, or related fields is an advantage. Sound knowledge of biotechnological processes in the area of manufacturing with mammalian cells. Strong communication skills, team player, motivated and solution-oriented. German required, English an advantage. Good GMP knowledge required. Day work with readiness to work outside regular working hours (including weekends). At Lonza, our employees are our greatest strength. With 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. Every idea, whether big or small, has the potential to improve millions of lives - and that is exactly the work we want you to be part of. Innovation thrives when people from different 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 transform our customers' groundbreaking ideas into actionable therapies, we look forward to welcoming you on board. Ready to help shape the future of Life Sciences? Apply now.