ppSwitzerland, Stein /p pThe actual location of this job is in bStein, AG, Switzerland /b. Relocation assistance is available for eligible candidates and their families, if needed. /p pJoin a dynamic, international team to perform routine analytical testing of Drug Products in a GMP environment, independently executing physical, chemical, and bioanalytical methods while ensuring accurate documentation and compliance with GDP and SOPs. /p pTake ownership of key lab activities (e.g. HPLC, CE‑SDS, UV, ELISA) and play an active role in building a new laboratory setup—bringing precision, curiosity, and a quality‑first mindset. /p pThis is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. /p h3What You Will Get /h3 ul liAn agile career and a dynamic work culture. /li liAn inclusive and ethical workplace. /li liCompensation programs that recognize high performance. /li /ul pIn addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. /p pThe full list of our global benefits can be found here: /p h3What You Will Do /h3 ul liResponsible to independently execute, coordinate and review physico‑chemical and biochemical assays under cGMP according to existing method SOPs (e.g. compendial testing/content/identity/purity for small molecules, biologics/large molecules) /li liResponsible to document assay execution under cGMP following Good Documentation Practices (GDP) and flag relevant observations to the supervisor for further assessment /li liAccountable for execution of operational tasks in the lab e.g. mobile phase preparations, calibration of equipment, adherence to and maintenance of 6S, consumable management and support of equipment maintenance. /li liSupport of validation and transfer activities in frame of new project introduction cGMP standards for audit readiness and supports onsite customer/regulatory audits /li liAssists in investigation/troubleshooting for assigned tasks /li /ul h3What We Are Looking For /h3 ul liFirst hands‑on experience in analytical methodologies like e.g. pH measurement, UV‑Vis, turbidity (experience with HPLC, Elisa or similar technologies are a plus) /li liExperience with GMP is a plus /li liApprenticeship or equivalent in Analytical Chemistry, Biochemistry or related field /li liFluency in written and spoken English, German is an asset /li liYou enjoy routine analytical testing and look for a chance to set up and shape a brand new laboratory with us /li /ul h3About Lonza /h3 pAt 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. /p pInnovation 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. /p pReference: R76448 /p /p #J-18808-Ljbffr
