Dược Phẩm & Sinh Học Y Tế - Mebiphar

Mô tả Công việc
Position Summary
Qualify the product in term of the requirement of customer, regulatory, safety and the international standard. Qualify the assembly line in term of the stability and the consistency.
He is responsible for finish goods audit and process audit at our suppliers. The QE also has the responsibility of helping our suppliers improve their products quality and quality system.
Key Responsibilities
Prepare the quality document to qualify the product.
Determine the checkpoint flow line of main assembly line. This includes the functional checking, appearance checking and safety checking.
Determine the sampling plan, inspection item and the reliability test plan
Prepare test plan and work with Eng. together on implementing the test plan
Collect and review the performance/reliability test data during Engineering build, Pilot run of new product.
Review and approval first article inspection of all critical components.
Hold production release meeting
Help other team members follow up customer complaints.
Active interactions with our supplier to improve products quality and the manufacturing process.
Prepare the quality document to qualify the product.
Determine the checkpoint flow line of main assembly line. This includes the functional checking, appearance checking and safety checking.
Determine the sampling plan, inspection item and the reliability test plan
Prepare test plan and work with Eng. together on implementing the test plan
Collect and review the performance/reliability test data during Engineering build, Pilot run of new product.
Review and approval first article inspection of all critical components.
Hold production release meeting
Help other team members follow up customer complaints.
Active interactions with our supplier to improve products quality and the manufacturing process.