Responsibilities & Duties 1.Be responsible for overseeing that the approved standard procedures have been implemented accurately and for ensuring that the production is done under the required conditions and the GMP standards are met. 2.Follow Environmental, safety and health guidelines. 3.Draft and revise packing material standard; review New Packing material art work. 4.Review the Batch Record, fill and sign the Inspection Record together with Batch Record. 5.Handle the rejected material and products, supervise the destroy process of the rejected material and products. 6.Inspect all the returned goods and fill the evaluation report. 7.To investigate customer compliant issue. 8.Complete Annual Product Review draft. 9.Be responsible for the management of raw material and product retention program; establish the product stability program and sampling plan and follow it‘s implementation; take out sample while need and make relevant record. 10.Supervise the product quality of EM. 11.Monitor the quality of material,and resolve the quality issue found in production with suppliers. 12.Supplier management, maintenance the approval supplier list. Relevant Education College or above, major in Chemistry, Pharmacy or Enterprise Management. Work Experience: At least two years experiences on process inspection, familiar with GMP management. Experience of quality inspection in pharmaceuticals is preferable. Abilities -Be working hard and active -Strong quality consciousness -Good interpersonal skill and communication skill -Good problem shooting and solving skills -Good team working consciousness -Good Learning ability -Have strong sense of responsibility and principle -Good English reading and expression ability -Be good at computer operation