A leading pharmaceutical company is seeking a QA Expert located in Neuenburg, Switzerland. The ideal candidate will have a Master's degree and 2-3 years of experience in cGMP operations within the Fill and Finish area, ensuring the quality of documentation and processes. Responsibilities include preparing controlled documentation, reviewing quality deviations, and approving aseptic interventions. Fluency in French and English is essential, with a strong emphasis on teamwork and autonomy. The role requires a minimum of four days on-site presence and may involve a 2-shift schedule during specific tasks.
#J-18808-Ljbffr