Deepak Chander Email & Phone Number

New Delhi, Dl, In

Delhi, India

* Quality management system,Internal audit related activities with other departments.* Product inspection and testing in coordination with sourcing team and design team.* Responsbile for ensuring product quality at vendor end by pre dispatch inspection as per inspection plan.* Product testing and validation for ensuring quality and reliability. * Market Complaint & COPQ data analysis ,MIS Preparation.* Driving quality initiative at vendor end like Project delight,Quality circle and daily work manager, improvement project based on data analysis. * New product development process monitoring and pilot batch inspection and clearance.* Vendor assessment and upgradation.* Product audit and process audit on periodic interval for ensuring satisfactory product and process performance on continuous basis.* Customer satisfaction assessment & feedback collection for improvement by visit to region,branches,dealer,godwans,service centr & ,customer visit.

Neemrana, Rajasthan, India

Responsible for supplier quality related issue of Room Air Conditioner Section.❖ Daily line loss discussion with supplier and update reason and take countermeasure on supplier quality issues. ❖ Facilitate root cause analysis and corrective action of supplier issue.❖ Review supplier manufacturing process, collaborate with supplier on process improvement and value enhancement opportunities.❖ Monitor and Manage supplier process quality performance and report quality metrics in form of Weekly meeting back to management.❖ Responsible for Warranty analysis and make investigation report for supplier failure part.❖ Support new product launches to ensure that supplier quality meets the required standards.❖ Support quality manager to monitor and report on supplier product quality and performance.❖ Report on key performance indicator (KPIs) in order to adhere to process and prevent occurrence of any non conformity relating to product, process or system.❖ Produce written report and make presentation.❖ Provide concise complete and accurate documentation of inspection result related to area ofresponsibility. In appropriate functional area, regulation engineering product specification or control plans, PPAP approval or product warrant submission.

Neemrana

1.Responsible for quality of Room Air Conditioner Section.2.Daily line loss discussion with production and update reason and take countermeasure on quality issues. 3.Man power planning for shift.4.Maintain KPIs for monitoring of processes and/or product quality perform analysis and interpret trends, identifying and activating on appropriate action as necessary.5.Design information control for any change in product6.Daily defect analysis and take countermeasure on defect.7.Preparing weekly analysis of defects.8.Closing of B kansa (inspection) CAR of current week.9.Responsible for Line audit & B kansa (inspection) CAR controlling.10.Responsible for market complain closer.11.Responsible for prepare weekly summary of pending line audit, line CAR and B kansa CAR for weekly Production quality meeting. 12.Root Cause analysis through simulation of possible causes.13.Conducting MQ (Manufacturing Quality Process Sheet) audit and process audits as per plan.14.Monitor and Manage process quality performance and report quality metrics in form of Weekly meeting back to management.15.Responsible for Warranty analysis and make investigation report.16.Helps to insure compliance to customer, regulatory, and third party registrants’ quality requirements. Participate in the audits from these bodies17.Monitoring the actions taken against the internal defects and customer concern

Manesar,Gurgaon

1.Ensuring the conformance to Quality for Product & Process. 2.Evaluating PPM trends on monthly basis.3.Conducting control plan and process audits as per plan.4.Documentation and data control as per IATF 16949:2016 and PDCA cycle5.Daily red bin analysis to find the cause of occurrence.6.Responsible for Non Conforming Material resolution. 7.Verify & record maintains any change in 4'M.8.Monitoring the actions taken against the internal defects and customer concern.9.Process optimization through 7 QC tools, SPC & CAPA.10.Eliminate Quality problem through QC tools. and initiate Corrective and Preventive action (CAPA)11.Ensuring the Document Control within the organization.12.Root Cause analysis through simulation of possible causes.13.Prepare Quality documents as per customer requirement.14.PFMEA review as per plan & RPN reduction as per Target.15.Document updates Like PFMEA, Control Plan, and Operation Standard as per customer Requirement.Rejection & Re-work Control through Continual improvement.16.Poke-yoke implementation on occurrence & detection stage.17.Verify all documents which is related to Process Quality.18.Monitor and manage process quality performance and report quality metrics in form of 19.MMCM,QRM,WRM etc. back to management.20.Raising Quality abnormality /Countermeasure in case of abnormality.21.Good understanding of technical Drawings.22.Suggestion and Kaizen implementation.23.Achieve PPM target as per AOP.

Sonipat, Haryana, India

1.In process Inspection Report generation for all component.2.Patrolling on line if non conformance observed on line Area.3.To give set up approval for Assembly line by FPA and LPA.4.Generation of reference sample/ limit sample.5.To maintain & Update In process Std with reference to the Drawing & Customer complaint.6.Final inspection of in house parts.7.Receiving countermeasure & effectiveness of Non Conformities feedback.8.To Handle Customer complaint and maintain the Customer complaint data.9.Continuous improvement in line for, quality, safety, and 5’S purpose.10.Process Improvement through Poke-Yoke, Kaizen.11.Responsible for availability of formats, Document & Master list updation.12.To maintain dock audit reports.