More than 6 years of experience in handling different kind of Pharmaceutical Validation Projects and 11 years of experience in Quality Control of Electrical Control PanelsDeveloping and implementing the Quality department’s strategy to ensure it meets the business requirements and customer deliverables, as well as ensuring the departmental performance against goalsQuality planning, process optimization, process standardization, troubleshooting and problem solving, identifying area of quality failure and taking steps for corrective and preventive actionsResponsible for Audit and Maintenance of ISO9001 system and documentation. Handling change control, CAPA. Review of CAPA effectiveness Preparation of audit report, review and approval of internal audit response, ensure implementation of internal audit CAPA and its effectivenessKnowledge of Validation Guidelines related to Computerized System like Data Integrity 21 CFR Part 11 and GAMP 5 for Pharmaceutical Industries.Handling vendor audits. Reviewing Technical Agreement from clients. Handling vendor audit checklist Review of calibration status of qualification instruments as per the schedule