Process/Aseptic Validation Engineer

Process / Aseptic Validation Engineer – Media Fill (m/f/d) 🚀 Take the next step in your pharmaceutical engineering career with Techfirm Engineering! We are currently looking for an experienced Process / Aseptic Validation Engineer – Media Fill (m/f/d) to contribute to exciting projects within the Swiss pharmaceutical industry. Are you an expert in Media Fill campaigns and aseptic manufacturing processes? Do you thrive in highly regulated GMP environments and enjoy working on technically challenging projects? Then this could be the perfect opportunity for you! 📍 Location: Near Basel, Switzerland Additional information regarding the project location and working arrangements will be provided during an initial conversation. 🎯 Your Mission As part of this assignment, you will play a key role in supporting the validation of aseptic processes on a sterile pharmaceutical filling line. Your main focus will be the planning, preparation, execution and follow-up of Media Fill campaigns (Aseptic Process Simulation – APS), ensuring that all activities meet applicable GMP and contamination control requirements. Working alongside Production, Quality Assurance, QC Microbiology and Validation teams, you will contribute to the successful delivery of critical project milestones and the reliability of aseptic manufacturing operations. 🔬 Your Responsibilities Coordinate and actively participate in the preparation, planning and execution of Media Fill campaigns (APS) within sterile manufacturing operations. Oversee campaign activities, monitor execution and collaborate with relevant teams to review and assess results. Contribute to aseptic process validation activities, ensuring consistent and reliable manufacturing processes. Maintain compliance with EU GMP Annex 1 and applicable Contamination Control Strategy (CCS) requirements. Support the investigation of deviations, perform root cause analyses and contribute to the implementation of effective CAPAs. Work closely with Production,