• To Roll out the QMS standards and ensure the training and implementation in respective domain
• To assess the maturity of the QMS in all domains based on existing on-field practices
• To identify and prioritize audits needs depending on customer risks, regulatory requirements and the QMS
maturity and guarantee the outcome of the corrective action plans,
• To execute yearly Audits comprising the System (IATF 16949 & ISO 9001), Start of Production readiness,
Conformity of Production & Specific Audits, including closure of non-conformities.
• Liason with the external certification bodies for IATF 16949, ISO 9001 for closure of Non-conformities
• To manage the QMS Documentation Repository comprising all Domains
• To Coordinate for Corporate Documentation Review Meeting with all relevant Stakeholders
• To coordinate for preparation of Quartely QMS Synthesis to Corporate team
• To ensure the implementation of Laboratory Management System.
• To coordinate for preparation of Weekly, Monthly, Quartely QMS Management reports