My key responsibilities are

To reduce market defect rate of PEL appliances.
To make efforts to reduce sale reduce sale return claims of Split AC and Microwave Oven.
To actively participate in Kaizen activities.
Ensure effective implementation of all applicable requirements of PEL Integrated Management System (IMS).

Quality, Health, Safety and Environment (QHSE) Department.

Studied ISO 9001: 2015 – Quality Management System.
Studied ISO 14001: 2015 – Environmental Management System.
Participated in internal quality audits under supervision of seniors. 
Participated in Health and Safety mock drills.
Studied complete process flow of refrigerator assembly.

Working on Medical Device Regulation (EU) MDR 2017/745.  My key responsibilities are

Preparing CE Mark Technical Documentation and EU Declaration of Conformity of medical devices.
Maintaining a Quality Management System compliant to EU MDR and ISO 13485.
Establishing, documenting, implementing and maintaining a Risk Management System according to EU MDR and ISO 14971.
Clinical Evaluation of Medical Devices according to MEDDEV 2.7.1 rev. 4.
Maintaining an effective Post Market Surveillance System for medical device.
Deploying HIBCC/ GS1 Unique Device Identification (UDI) codes system for post market traceability of medical devices.

Worked with Injection Molding machines and Hydraulic Presses to manufacture rubber parts for automotive industry.

Studied complete process flow of Transformers manufacturing.