Beschreibung
Validation Engineer - Solothurn, Switzerland
Must have:
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
Purpose:
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