Coordinate all activities for identification, collection, indexing filling and storage related to the Document Control procedure, including QC documents. (E.g. CPIS, DR, RIR)
Input document data into the standard registers ensuring that the information is accurate and up to date.
Maintain updates records of all approved documents....
Understand and audit on production line process and equipment setup. Ensure all the documents (PWI) used for process are tally with BOM/Engineering and assembly drawing.
Inform the superior and concerned departmental representatives on the nature of non-conformance detected during auditing....
· Maintain and control QA/QC practices with regular checks and inspections ensuring correct operation and implementation of procedures.
· Develop and determine all standards to perform inspection and tests on all procedures and oversee all testing methods and maintain high standards of quality for all processes.
· Accountable for the quality and workmanship of site activity, good knowledge of all aspects of engineering construction relating to architectural and structural discipline interfacing the multidisciplinary processes....
Coordinate all activities for identification, collection, indexing filling and storage related to the Document Control procedure, including QC documents. (E.g. CPIS, DR, RIR)
Input document data into the standard registers ensuring that the information is accurate and up to date.
Maintain updates records of all approved documents....
Mengeluarkan memo atau e-mel kepada Jabatan Pengeluaran bagi produk yang tidak memenuhi spesifikasi melalui sistem Vertech. Memastikan proses penolakan (cavity rejection) diaktifkan bagi produk yang telah disahkan tidak memenuhi spesifikasi dan dikekalkan sehingga pemeriksaan semula menunjukkan keputusan LULUS.
Menyediakan laporan kualiti setiap jam serta menjalankan audit packed ware dan pemeriksaan secara rawak sebelum produk dihantar ke palletiser.
Memaklumkan kepada Cold End Specialist dan Penyelia QA mengenai sebarang kecacatan utama atau kritikal yang dikenal pasti semasa pemeriksaan dan persampelan....