【COMPANY OVERVIEW】
A leading precision oncology company focused on helping conquer cancer globally through use of its proprietary blood tests, vast data sets and advanced analytics.
【JOB RESPONSIBILITIES】
- Lead to and maintain regulatory approvals for In Vitro Diagnostic (IVD) devices and medical devices.
- Lead in planning regulatory strategy for Japan.
- Assist in meeting and consultation activities to gain PMDA’s feedback.
- Acquire and stay up to date with knowledge on applicable regulatory requirements and scientific/technical issues of assigned projects.
【REQUIREMENTS】
- B.S./B.A. in a science, engineering, or related technical field.
- At least 3 years’ experience in regulatory affairs in Pharma, IVD and medical devices industry. CDx regulatory experiences are preferred.
- Fluent Japanese and Business Level English
【FOR FURTHER INFORMATION】
- Click apply
OR
- Contact Saloni: