Description
MEDICAL DEVICES: Regulatory Affairs SpecialistResponsibilities:
- Supporting the internal Regulatory Affairs with Technical File documentation
- Reviewing of Risk Management Documentation
- Going through labelling and marketing material
- Ensuring that the company's products comply with the regulations of government agencies
Requirements:
- Profound knowledge of European Medical Device Regulations (93/42/EEC)
- Experience with Risk Management Documentation for medical devices according to EN ISO 14971:2012
- 2-3 years of experience in European Medical device industry especially with regulatory, labelling, quality or engineering
- Excellent command of English and German.
You can expect a challenging and varied job in a multicultural environment. If this is something you are interested in please send your CV to Ms Sarah Tomasella, If you have any questions please feel free to contact us on . We look forward to hearing from you.
Best regards from Zurich,
Sarah Tomasella