Medical Device FDA Regulatory Consultants
🏫 KBIO Solutions
📍Seoul, South Korea
💰 Competitive Salary
English / ESL / TEFLJob Description:
KBIO Solutions is currently looking for a Medical Device FDA Regulatory Consultant in Seoul, South Korea. The consultant will work closely with Korean medical device companies to handle US FDA and EU CE regulatory submissions.
Position Overview:
Responsibilities include learning US FDA and EU CE medical device registration requirements, clinical trial monitoring, and statistical analyses. The consultant will lead and manage medical device registration projects, informing client companies of registration needs and compiling submission files. Collaborating with client representatives, the consultant will tackle challenges to ensure successful registration processes.
Qualifications:
- Candidates should have a graduate degree, be college graduates, or current graduate students
- Proficiency in Korean and English
- Academic background from a reputable institution, high motivation, good attitude, and attention to detail
To apply, please send your English or Korean resume to kyungyoon.kang@kbiotechsolutions.com. Application submissions are ongoing, and only short-listed candidates will be contacted for an interview.
👉 Apply Here: kyungyoon.kang@kbiotechsolutions.com
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