My client is a global medical device company, headquartered in the US, specialising in Orthopaedics and General Surgery medical devices.
They are looking for a RAQA expert for their Korea Team.
Responsibilities:
- Registration of new products
- Review and attaining of KGMP certificates
- KGMP Submission
- Review and analyse existing licenses
- Quality Management
- Regulatory compliance
Requirements:
- Bachelor's degree
- At least 5 years of experience in RA in medical device industry
- Bilingual
- Good communication, organisation and negotiation skills
If you are interested, please apply with your CV attached.
