As Qualification & Process Engineer you will be working as part of the CordenPharma Fribourg Technical Operations Department. You will manage the qualification plan to maintain the accurate qualification state of new and existing equipments for Manufacturing, Packaging & Engineering. 

• Qualification of equipments : you will execute and monitor the qualification status of the new and existing manufacturing, packaging & engineering equipments and systems, manage the whole process of qualification plan (URS/DQ/FAT/SAT/IQ/OQ/PQ) & create qualification, risk analysis, technical &SOPs documentation
• Improvements: You will lead or participate to investigations, improvements and customers requests implementation for equipment and systems under your responsibilities.
• Leadership : You will manage external resources (equipment suppliers) and project teams
• Quality: you will ensure the quality of Qualification activities activities according to GMP guidelines, VMP and internal procedures
• Process: Lead the investigation for deviations linked to equipment and production processes using problem-solving tools and define corrective actions
• Projects: Lead or participate to the implementation of continuous improvement projects for manufacturing and packaging equipment and processes