Beschreibung
For a 4 month project with our customer in Basel, we are looking ASAP for a
Validation Engineer
Tasks:
Independent planning and execution of all required activities for qualification/validation of equipment, special processes and production processes. Independent creation of all required qualification/validation documents in cooperation with production, product development, design transfer and quality engineering. Serves as technical expert for the Validation process and responsibilities to ensure compliance. Ensure that all validation activities are carried out and reported in a timely manner. Ability to execute Validation processes and Testing. Requirements:
Fluent GERMAN is essential for this position and advanced English. 3 Years proven qualification/validation experience in the medical devices production environment. Experience in Process Validation, Medical Devices, 21 FDA 820, ISO 13485. Engineering background. Analytical, innovative and pragmatic thinking. Some flexibility in working hours is required. Able to follow change management for internal guidelines. Are you interested in this position? Then we are looking forward to receiving your application.