The manufacturer/fabricator is responsible for the quality of all their Manufactured and & Fabricated products, which includes not only goods workmanship, but also compliance with all codes, standards and specifications contained in the contractual agreements. This is regardless of whether …
Normally 4 weeks after placement of order or 2 weeks after submitting the critical documents, a kick off meeting is held. It is advisable to hold the KOM after one cycle of critical document turnaround in order to have …
Short listed bidders are invited for a face to face meeting with the client called clarification meeting or pre-purchase meeting at client’s premises. The intention of such meeting is: To explain what is wanted from the supplier and how …
As potential supplier’s proposal are received, they are reviewed by procurement (to see if supplier could adhere to the stipulated delivery and compare price with other suppliers); by quality engineer (to see if supplier is prepared to abide by the …
Depending on the criticality and complexity of the materials & equipment being procured, CLIENT and their assigned representatives may conduct out a pre-award audit or assessment of CONTRACTOR & VENDOR and any intended lower-tier- Supply Chain prior to the award …
Normally, 2-4 weeks after the kick off meeting or 2 weeks after submission of critical quality documents, the pre production meeting is held. It is advisable to hold the PIM after one cycle of critical document turnaround in order to …
Kick Off meeting: Normally 4 weeks after placement of order or 2 weeks after submitting the critical documents, a kick off meeting is held. It is advisable to hold the KOM after one cycle of critical document turnaround in order …
Inspector Duties: The manufacturer/fabricator is responsible for the quality of all their Manufactured and & Fabricated products, which includes not only goods workmanship, but also compliance with all codes, standards and specifications contained in the contractual agreements. This is regardless …
Inspection reports shall be written on a template in order to standardize the reporting system. Such form normally has sections for vendor details, reference document (QC procedures, drawings and specially); description of what activity was witnessed or inspected and the …