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