Quality Engineer / Manager

JD for Quality Engineer / Manager:

The Quality Engineer / Manager reports to the MD on the effectiveness of his actions.

• Identify and evaluate activities that may give rise to problems regarding Quality.
• In addition to the assigned duties, QM is responsible for implementing of MS, preparation and changing of documented information including quality Manual, System & Procedures, SOP and get it approved by the managing director, He will be the ISO coordinator[MR] for the company and interact with consultants certification body, and regular implementation of ISO 9001-2015 standards.
• Recommend, urge for and propose solutions to problems and make sure that the solutions chosen are carried out.
• Propose actions to prevent possible product non-conformities
• Make certain that the non-conformities have been resolved.
• Evaluate the appropriateness and efficiency of the QMS adopted.
• Interact with external agencies on issues related to the processes identified in the Quality Management System.
• Prepare the Root Cause Analysis (RCA) using 8D analysis, Corrective and Preventive Actions (CAPA) by discussing with PM, PE, PRM and all related departments for all quality problems.
• Adopting to the MR role & Quality Management system, QM is responsible for conducting of internal audits to each and every department.

- Specific tasks include:

• Prepare / update this QMS Manual, instructions, Procedures and modules, related to various activities
• Carry out inspections to verify the application of QMS procedures.
• Sub supplier certification to be uploaded or shared to client in the form of MDR, SPIR, Instruction Manual & TRS.
• Analyze the non-conformities with the concerned PM, PE, PRM, PDM, etc, and close the non conformities with proper corrective actions.
• Responsible to receive, record & handle customer complaints
• Prepare the Root Cause Analysis (RCA) using 8D tool for necessary NCs and customer complaints and classify them under the below causes
• Lack of Training
• Manufacturing /assembly faults
• Change control not communicated
• Purchasing / Supplier faults
• Quality in Testing
• Documentation
• Maintenance
• Others, Corrective Actions and Preventive Actions (CAPA) with the respective PM, PE, PRM, PDM, etc, and implement the same for the improvements.
• Ensure that the Preipolars products meet the conformance with TRS (Technical Regulation and Standards) requirements as per the applicable countries.
• Ensure and approval for the production stage inspection.
• Final authority to release product with good quality.
• Ensure the Statutory and Regulatory requirements are covered.