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f.2  Corrective action

                           f.2.1  Where process or system related non-conformities occur they shall be
                                  brought to the attention of the relevant department head / project engineer
                                  who shall raise as non-conformance report detailing the non conformance.
                                  Product related non-conformance reports shall be raised in accordance
                                  with control of non conforming products procedures.

                           f.2.2  The department head / project engineer, in conjunction with others where
                                  necessary, will then investigate the non-conformance for the purposes of
                                  identifying the root cause of the problem and record the findings on the
                                  non-conformance report.

                           f.2.3  Having identified the root cause of the problem the department head /
                                  project engineer responsible for the department in which the problem has
                                  been identified will implement corrective action commensurate with the
                                  magnitude of the problem encountered and record such details on the
                                  non conformance report. Any such corrective action that effects further
                                  processes or other departments must involve discussion with and have
                                  the agreement of such department heads / project engineers.

                           f.2.4  All non-conformance reports raised for either product, system or process
                                  related problems shall be copied to the management representative who
                                  shall maintain a register of all such reports received. This includes those
                                  raised, during internal audits.

                           f.2.5  Copies of  customer  complaints  and non-conformance  reports shall  be
                                  reviewed  by the  management  representative  to  ensure  that  the  non-
                                  conformity has been analysed in order to determine the root cause, that
                                  the magnitude of the non-conformance has been evaluated in relation to
                                  the  potential  impact  on  product  and  quality  costs,  performance  and
                                  customer satisfaction, and that any corrective action taken is suitable to
                                  prevent recurrence.
                           f.2.6  Where corrective action taken is found to be suitable the reports shall be
                                  filed for follow-up purposes (see clause f.2.9 below.) where it is not the
                                  management representative shall discuss the application of more suitable
                                  corrective action with persons as necessary. This review and an subsequent
                                  corrective action should be recorded on the customer complaint or non-
                                  conformance report.
                           f.2.7  The  management  representative  shall monitor  corrective actions  and
                                  expedite any such actions that become overdue. Where overdue corrective
                                  actions  become  excessive  the  matter will  be referred  to  the  General
                                  manager for further intervention.

                           f.2.8  Where  the  corrective  action  resulting from  customer  complaints  non
                                  conformance  involves  a  subcontractor  / supplier’s  grading or  required
                                  changes to quality system documents, such matters will be carried out in
                                  accordance  with  purchasing  or  document and  data control  procedure
                                  respectively.

                           f.2.9  The management representative may initiate unscheduled audits to verity
                                  the  implementation  and  effectiveness  of  corrective  acitons  taken
                                  implementation and effectiveness of corrective actions required as a result
                                  of internal quality audits shall in all cases be verified through follow up
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