QCAssociate

The actual location of this job is in **Stein, AG, Switzerland**. Relocation assistance is available for eligible candidates and their families, if needed. Join 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. Take 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. Check out [Your Career in Drug Product Services at Lonza](https://www.youtube.com/watch?v=gEXvtbcdNdA&list=PLh3u2rKfWyIfXC2d2O3enUrpMjjJ7DO_x&index=5)! This 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. **What you will get:** * 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 lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: **What you will do:** * Responsible 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) * Responsible to document assay execution under cGMP following Good Documentation Practices (GDP) and flag relevant observations to the supervisor for further assessment * Accountable 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. * Support of validation and transfer activities in frame of new project in