- We are looking for a "Technical Service Team Leader" for our client, a company operating in the medical device sector in Ankara.Manage and organize the processes of the Technical Service team.Actively participate in post-sales processes, including the transfer, transportation, installation, training, and inspection of our devices.Provide technical support services for malfunctioning medical devices on-site or at the office by carrying out maintenance and rWe are looking for a "Technical Service Team Leader" for our client, a company operating in the medical device sector in Ankara.Manage and organize the processes of the Technical Service team.Actively participate in post-sales processes, including the transfer, transportation, installation, training, and inspection of our devices.Provide technical support services for malfunctioning medical devices on-site or at the office by carrying out maintenance and r
- Medikal sektöründe faaliyet gösteren iş ortağımız için İthalat ve Lojistik Sorumlusu arıyoruz.Müşteri ilişkileri yönetimi ve ithalat süreçlerinin düzenlenmesi,Depo yönetimi ve ihracat organizasyonunun sağlanması,Talep planlama ve süreç optimizasyonu yapılması,Ekip yönetimi ve performans takibi,Gerekli raporlama süreçlerinin güncel tutulması ve analiz edilmesi.Medikal sektöründe faaliyet gösteren iş ortağımız için İthalat ve Lojistik Sorumlusu arıyoruz.Müşteri ilişkileri yönetimi ve ithalat süreçlerinin düzenlenmesi,Depo yönetimi ve ihracat organizasyonunun sağlanması,Talep planlama ve süreç optimizasyonu yapılması,Ekip yönetimi ve performans takibi,Gerekli raporlama süreçlerinin güncel tutulması ve analiz edilmesi.
- We are looking for an ‘International Regulatory Affairs Specialist’ for our client operating in the medical device industry.As an International Regulatory Affairs Specialist, you will be responsible for ensuring that medical devices comply with global regulatory requirements, including FDA, EU MDR, and ISO standards. You will manage regulatory submissions such as 510(k), PMA, and CE Marking applications, and serve as the point of contact with regulatory agWe are looking for an ‘International Regulatory Affairs Specialist’ for our client operating in the medical device industry.As an International Regulatory Affairs Specialist, you will be responsible for ensuring that medical devices comply with global regulatory requirements, including FDA, EU MDR, and ISO standards. You will manage regulatory submissions such as 510(k), PMA, and CE Marking applications, and serve as the point of contact with regulatory ag
