keyboard_arrow_down
warning
İlan yayından kaldırılmıştır
İstanbul(Avr.)
İş Yerinde
İş Yerinde
Job Type
Full-Time
Position Level
Specialist
Department
Engineering
Engineering
Application Count
325 application
Job Type
Full-Time
Position Level
Specialist
Application Count
325 application
Department
Engineering
QUALIFICATIONS AND JOB DESCRIPTION
Education: Graduate Bachelor’s degree or country equivalent in Engineering or Science (Biology, Chemistry.. etc) or related scientific discipline, or equivalent
Licenses/ Certifications: Regulatory, Quality, ISO certificates (if app.)
Experience: Typically, a minimum of 1-3 years of related Regulatory Affairs experience
Excellent oral and written communication skills both in English and Turkish
Consistently neat and accurate reporting
Excellent organizational skills
Proficient in MS Office applications
Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies to advise on the submission strategy
Timely compile materials for license renewals, updates and registrations
Review labelling and labels for compliance with regulatory requirements
Review changes to existing products and SOPs to define the requirements for regulatory submissions
Timely compile materials for license renewals, updates and registrations
Responsible for product submissions, license renewals, periodic updates and registrations
To knowledge the new MDR system and response on time for the changes/ revision / re-registration
To report quality (recall, adver event report etc.) to MoH on time
Contact with Supply chain, Quality, Marketing
Licenses/ Certifications: Regulatory, Quality, ISO certificates (if app.)
Experience: Typically, a minimum of 1-3 years of related Regulatory Affairs experience
Excellent oral and written communication skills both in English and Turkish
Consistently neat and accurate reporting
Excellent organizational skills
Proficient in MS Office applications
İŞ TANIMI
Conducts reviews of product and manufacturing changes for compliance with applicable regulationsCollect and coordinate information and prepare regulatory documentation for submission to regulatory agencies to advise on the submission strategy
Timely compile materials for license renewals, updates and registrations
Review labelling and labels for compliance with regulatory requirements
Review changes to existing products and SOPs to define the requirements for regulatory submissions
Timely compile materials for license renewals, updates and registrations
Responsible for product submissions, license renewals, periodic updates and registrations
To knowledge the new MDR system and response on time for the changes/ revision / re-registration
To report quality (recall, adver event report etc.) to MoH on time
Contact with Supply chain, Quality, Marketing
Preferred Candidate
More than 1 years of experience
Bachelor’s(Graduate), Master’s(Student), Master’s(Graduate), Doctorate(Student), Doctorate(Graduate)
Ruhsatlandırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.
Ruhsatlandırma Uzmanı Ruhsatlandırma Uzmanı Maaşları Ruhsatlandırma Uzmanı Nasıl Olunur? Ruhsatlandırma Uzmanı Nedir? Ruhsatlandırma Uzmanı İş İlanları
Hakkımızda
Randstad, İK hizmetleri sektöründe dünya lideridir. İnsanları ve kuruluşları gerçek potansiyellerini gerçekleştirmelerinde destekliyoruz. Bunu, günümü
Şirket Sayfasına GitŞirketin Aydınlatma Metni
Detaylı BilgiYan Haklar
Özel Sağlık Sigortası.
Ruhsatlandırma Uzmanı pozisyonu ile ilgili daha detaylı bilgi almak ya da diğer iş fırsatlarını incelemek için aşağıdaki sayfaları inceleyebilirsiniz.
Ruhsatlandırma Uzmanı Ruhsatlandırma Uzmanı Maaşları Ruhsatlandırma Uzmanı Nasıl Olunur? Ruhsatlandırma Uzmanı Nedir? Ruhsatlandırma Uzmanı İş İlanları