The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a Compliance Engineer at our sterile manufacturing site in Stein, Canton Aargau, you will play a key role in ensuring GMP compliance across systems, equipment, changes, and CAPAs. In this position, you will act as a central point of contact for GMP-related topics, support inspections, and ensure that all regulated systems meet internal operational requirements as well as external regulatory 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. Our full list of tailored local benefits can be found below. Benefits in Stein: What you will do: Create and review GMP documentation such as periodic reviews, qualification documents, and SOPs Prepare presentation materials and organize subject matter experts (SMEs) for audits and inspections Communicate effectively with internal inspection teams and support inspection readiness Define, assess, and oversee GMP-relevant activities within CAPA and change management processes Lead the full lifecycle of CAPAs and changes from creation through execution Support re-qualification activities and ensure documentation accuracy Represent the Engineering Lead Team by taking over delegated GMP-related duties What we are looking for: Bachelor’s degree or equivalent qualification in Pharmacy, Engineering, or a related technical field Strong experience in the pharmaceutical industry with focus on GMP and engineering environments Solid project management skills Excellent communication abilities and