Job summary
| Job category | Technical (Sales / Design / Development / Production Control)／Production Control / Quality Control / Construction Control / Environment, Health, and Safety / Postmarketing Surveillance |
|---|---|
| Industry | Health Care／ Medical Equipment |
| Employment type | Uncategorized |
| Position level | Director or Above |
| Number of openings | 1 |
| Desired entry time | - |
| Required language skill | |
| Foreign language competence | - |
| Working hours | Others |
| Welfares / Leave systems | |
| Assistance in visa application | - |
| Number of foreign employees | - |
Work details
Company Overview: Company develops medical technology in following areas: cardiac rhythm management, atrial fibrillation, cardiovascular and neuromodulation. Product portfolio includes implantable cardioverter defibrillators, pacemakers, electrophysiology catheters, mapping and visualization systems, products for structural heart and vascular diseases, and spinal cord stimulation devices.
Job Contents:
The professional will be in charge of post-market surveillance for assigned products according to PMDA/GVP ordinance.
Safety information gathering and evaluation, planning and implementation on safety measures (PMDA reporting, recall etc)
Requirements:
At least 3 years of experience in Safety Surveillance space (GVP)
Business Level English
Degree in Scientific field
Knowledge of ISO13485
Experience in RA/QA/QC or PMS work in medical device industry
Carduivascular experience preferable
About interview
Liaison
Safety Surveillance Specialist || 安全管理グループスペシャリスト
RGF HR Agent
600 〜 900 ten thousand JPY
