https://bayt.page.link/cWob23BNq7vtwspX7
أنشئ تنبيهًا وظيفيًا للوظائف المشابهة

الوصف الوظيفي

Areas of responsibility include: 
  • Leading the Complaint assessment board meeting to review, assess and report of incoming complaints.
  • Leading/participating in the reporting decision meeting in case of potential adverse events
  • Initiating and timely monitoring of Complaint investigations, information- or complaint part requests
  • Review and evaluation of investigation results.
  • Communication of complaint investigation results and closure of Complaints
  • Coordination of complaint management and reporting activities according to legal, normative and internal requirements
  • Provide information of reportable Adverse Events to Regional Reporting Unit
  • Maintenance of Complaint File, Adverse Event and Field (Safety) Corrective Action records
  • Maintenance of internal process documents
  • Support or participation in internal and external audits
  • Entry point of authority communication
  • Reporting of authority communication to management and involved parties

Qualification and experience:
  • Technical diploma
  • Knowledge of the relevant complaint and vigilance related processes in foreign markets like Europe, USA, China etc.
  • At least 2 years of professional experience in the field for medical devices.
  • Intercultural experiences especially working in a global multi-site team across countries
  • Structured, reliable and goal-oriented way of working.

لقد تجاوزت الحد الأقصى لعدد التنبيهات الوظيفية المسموح بإضافتها والذي يبلغ 15. يرجى حذف إحدى التنبيهات الوظيفية الحالية لإضافة تنبيه جديد
تم إنشاء تنبيه للوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.
تم إلغاء تفعيل تنبيه الوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.