09-2015 - Now
Personal services Responsible for overall Quality Management System (QMS) of ISO department for review of documents related to Quality.
Achieves quality assurance operational objectives by contributing information and analysis to strategic plans and reviews; preparing and completing action plans;
SOP preparation, maintenance of technical documentations as per ISO: IEC 17025:2005 & ISO: IEC 17043:2010 including preparation of policies. Review, Change and Distribution of Standard Operating Procedures (SOP’s), Specifications and Quality Formats.
Revision of Quality Manual, Procedure Manual, SOPs during Surveillance audit and Re- Assessment audit of ISO/IEC 17025:2005 & ISO: IEC 17043:2010
Maintains and improves product quality by completing product, system, compliance and surveillance audit; investigating complaints; collaborating with other members of management to develop new product and design.
Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions and verification procedures; monitoring inventories.
Archival of Dope Control records and reports including preparation and revision of Quality Formats and Cross check Formats of New Documents.
Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes with its corrective actions, re-validations and updating of master list.
Responsible for implementation of facility audits on a regular basis.