Manage and coordinating the process verification and validation activities, internally and/or with corporate team, according to FDA and all other global regulatory agency requirements.
Perform supplier selection, qualification and evaluation which include site audit as needed. Monitor supplier performance or corrective/preventive action pertaining to quality issue or failure of incoming inspection.
Perform and co-ordinating the internal quality audit program and external audit as per schedule. Co-ordinate and close all any corrective/preventive action pertaining to the audit.
Participate/co-ordinate the design process and new product launches, including Operations training, FMEA and Control Plan development to ensure that expectations for quality, performance, regulatory compliance, and delivery are met.
Identify areas of improvement within the organization and drive to completion with by establishing partnership with applicable departments. Provide and initiate training programmers to new products and set process parameters.
Use appropriate quality tools as part of multifunctional team (such as FMEA, and Gage R&R analyses) to solve problems identified during quality assurance activities. Monitor product performance and institute methods to reduce variability.
Ensure that appropriate testing, measurement, calibration and analytical equipment and methodology is used for quality assessment; serve as a metrology resource.
Address customer complaints to assure that root cause analysis and proper corrective action/preventive actions are taken, and results are communicated to the customer and all other appropriate parties in a timely manner.
Assist Management in developing & maintaining the QMS procedures & work instructions in compliance with ISO13485, GMP and other regulatory quality standards.
Perform failure analysis and ensure that timely corrective/preventive action is taken
Requirements:
Bachelor degree or equivalent certification preferred.
2+ years QA experience, preferably in a corporate environment.
Knowledge of ISO13485 and FDA requirements for Medical Devices.
Knowledge of quality management system software application.
Meticulous, analytical and able to work independently