· To implement and maintain the Quality Management System ( QMS )
, auditing processes and timely closure of 8D , Corrective and Preventive
Action( CAPA) Reports , Audit Action both Internal & External NCs
· To provide full Quality support to all departments to ensure
that they are familiar with the various QMS and its documentation
· To ensure that all documents are transferred from external to
internal ( customer or supplier )
· To co-ordinate with all the departments and conclude the early
closure of audit/CAPA findings
· Development and review of an overall Quality Management to
ensure conformance to processes, procedures, specifications and regulatory
requirements, to be extended to EHS & Quality.
· Implementation and certification of the Quality Management
System according IATF16949 /ISO 9001/ISO14001/OHSAS18001 etc.
· Control of product documentation and production floor paperwork
related to IATF16949/ISO14001/OHSAS18001
· Co-operation with cross functional team in terms of all quality
related issues like audits, complaints, etc.; internal audits etc.
· Co-ordinate implementation of all documents/changed documents
including customer specifications through document control programme
· Update documents, monitor changes, monitor the document approval
process
· Administer current controlled hard copies when necessary eg: ISO
manuals , customer specific requirement documents
· Review current Quality related policies, procedures, work instructions
and forms to define areas of improvement. Ensure that these documents are
reviewed by other process owners as well
· Ensure that the obsolete documents are electronically archived
in relevant databases
· Co-ordinate electronic document and data control awareness
training
·
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