Responsable qualité

• Apr 2006 - Present

. Apply, maintain and upgrade the quality management system on site in relation to international standards to medical devices manufacturing . Develop documentation in relation to Corporate Quality Management system . Ensure communication between the two other subsidiaries situated in France . Ensure communication and understanding among staff . Manage non-conformities in collaboration with Quality Corporate and site Director . Participate in the evaluation of suppliers or service providers . Write protocoles and operating manuals for the activities to follow . Ensure follow-up, application and vérification of the efficiency of corrective and preventive actions set in place . Carry out internal audits . Participate in the development of risk management . Participate in the management of change control . Follow-up of quality indicators in relation to quality control, production and metrology . Prepare management review . Supervise management system of mesurement and control equipments in collaboration with the Metrology Manager . Supervise the environmental control (particles contamination, biocontamination aero-biocontamination) . Participate in training of staffs . Etc. Show less