Contractor Regulatory Affairs Manager (m.f.d )
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Switzerland |
Temporary Employment
Zu besetzendes Projekt: Contractor Regulatory Affairs Manager (m.f.d )
Branche: MedizintechnikFähigkeiten: Head of Regulatory Affairs,Chinese,Chinese Regulations,clinical trials
Projektstart: 01.03.2024
Projektdauer: 12 months
Auftragsvolumen: 2016 Hour(s)
Einsatzort: Switzerland
Aufgaben:
- Develop product registration and clinical trial strategies in East Asia (e.g. China, Taiwan, Hong Kong)
- Responsible for registration activities, coordination of internal departments
- Observe and report on regulatory changes and best practices in East Asia
- Manage clinical trials in East Asia with 3rd party service providers (CRO/SMO)
- Establish and maintain relationships among company, sales partner and authority
Qualifikationen:
- Ideally 2+ years’ experience in medical devices regulatory affairs and registration in China
- University Degree in Biomedical Engineering or Medicine
- Able to work under pressure in a changing environment with flexibility, team player
- Fluency in English mandatory in writing and speaking
- Ideally Mandarin Chinese in writing and speaking (C1 or higher); ideally German in speaking and reading (B1 or higher)
Referenznummer: 14041
Branche: Medizintechnik
Beginn des Projekts: 01.03.2024
Dauer: 12 months
Anstellungsart: Temporary Employment
Kontakt
Gaziza Konuspayeva