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