(a) the implementation of national standards, industry standards and enterprise standards for medical devices.
(two) to establish and improve the quality management system, so that it can operate effectively and continuously. (The quality management network diagram is as shown)
(3) Report the quality operation to the general manager's office.
(four) the acceptance of goods in storage, to determine the qualified goods in storage.
(five) to participate in the examination of commodity suppliers and determine qualified suppliers.
(six) to be responsible for the transmission of commodity quality information with suppliers.
(seven) responsible for the timely disposal of customer complaints and adverse reactions to the quality of goods.
(eight) according to the regulations on the supervision and administration of medical devices, modify and formulate quality documents.
(9) Collect relevant product quality standards and file them.
(ten) have the right to refuse to sign for unqualified goods.
(eleven) have the right to reject unqualified suppliers.
If it is a manufacturing enterprise, you are asking me, and I will call you back.