Qualifications: · Bachelor degree in Engineering and technical or Health/Life Sciences departments of universities. · Preferably 2 to 3 years experience in Regulatory Affairs Management in a multinational environment (medical industry would be an asset). · Working knowledge of regulatory registrations in Turkey or other countries. · Working knowledge with ISO 13485, MDD (93/42/EEC), FDA requirements and the other global regulations. · Knowledge in MS Office software (Word, Excel, Powerpoint, Outlook), and SAP is required. · Excellent command of written & spoken English is compulsory. · Team player with excellent communication and presentation skills; able to develop collaborative relationships with various stakeholders both internal and external to achieve objectives. · Analytical thinking, result and solution oriented, innovative, proactive, flexible and strong ability on problem solving and reporting. Must be able to identify creative options for resolving issues that respond to multiple stakeholder interests and needs, · Strong planning, follow up, reporting, coordination and organization skills to achieve accurate and timely results. · No military obligation for male candidates. · Be confident, positive, self-motivated& able to work independently · Be a good teamplayer · Good communication skills · Teamwork oriented, ability to establish and maintain effective working relationships\ willing to learn |