Ziemer Ophtalmology

Regulatory Affairs Manager (f/m) 100%


  • 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


  • University degree or above in biomedical engineering, medicine or similar discipline
  • Ideally 2+ years’ experience in medical devices regulatory affairs and registration in China
  • Advanced MS-Office skills
  • Self-motivated, excellence in work planning and time management, attention to detail
  • Able to work under pressure in a changing environment with flexibility, team player
  • Fluency in English mandatory in writing and speaking (B2 or higher)
  • Ideally German in speaking and reading (B1 or higher); ideally Mandarin Chinese in writing and speaking (C1 or higher)

We offer you an exciting challenge in the growth-oriented market of medical technology. As a committed and proactive personality, you can play a formative role in the future of our dynamic company. Interested? Then we look forward to receiving your complete online application including CV, letter of motivation, references and diplomas.

Please note, that only complete applications will be considered. Uncomplete applications will not receive feedback. Applications from recruitment agencies will not be considered.

If you have any questions regarding tasks and requirements, please contact Michela Peisino, michela.peisino@ziemergroup.com. For information on HR topics, Ms. Brigitte Lüscher, Human Resources, will be happy to assist you on 032 332 70 70.

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