Multinational company in the healthcare industry is looking for a for its site in Lazio.
He/she wil be responsible for:
Supervision of Design and Development activities by transferring the design inputs to the product to be developed.
Writing and review of verification and validation plans, protocols and reports.
Qualification of the processes to be performed and the equipment to be used for the manufacturing to the device.
Transfer the design to the manufacturing department in order to ensure the quality of the product to be manufactured.
Ensure that every part of the project is conducted in compliance with Design Control as prescribed by ISO 13485