【COMPANY OVERVIEW】
A US based company focused oncology diagnosis
【JOB RESPONSIBILITIES】
Responsible for maintaining regulatory approvals for medical devices in Japan
Consultation with PMDA and creating strategies in line with their feedback
Review labelling
Development and review of SOPs
Analyse regulatory challenges before they arise and provide solutions
【REQUIREMENTS】
Minimum of 2 years of experience in regulatory affairs. (IVD/Medical Device preferred)
Japanese and English abilities
【FOR FURTHER INFORMATION】
Click apply
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Contact Pauline