**QUALIFICATIONS** + Graduated from universities' Science or Engineering (biology, chemistry, etc.) Departments + Quality management system standard experience (EN ISO9001,EN ISO13485) + Preferably, experience in the field of medical device quality management system and medical device regulation, + Preferably having knowledge and experience in statistics and reporting, + Medical sector experience is an asset, + Full Professional Proficiency in English + Good at Office Applications & Computer + Strong communication and negotiation skills, + Dynamic, disciplined and focused to responsibilities, + Preferably not exceeding 40 + Will be able to reside in Antalya + For male candidates, there is no military obstacle **JOB DESCRIPTON** + Supporting Quality Assurance Department on the evaluation of the effectiveness and efficiency of the quality management system, mainly with focus on the change management, pFMEA and validation activities including software, + Supporting Quality Assurance Department on the implementation of EN ISO 9001,EN ISO 13485 standards to current production process and practices as required, helping training organizations + Presents or arranges for the presentation of training on quality system topics. + Contribution to the definition and implementation of QS relevant projects + Contribution to the implementation of QS relevant software support + Collaborate in projects and teams as appropriate