Job summary
| Job category | Administrative (Human Resources / Finance / Legal / Public Relations)／Legal Affairs / Intellectual Property / Credit Management / Compliance |
|---|---|
| Industry | Health Care／ Other Health Care |
| Employment type | Uncategorized |
| Position level | Other |
| Number of openings | 1 |
| Desired entry time | - |
| Required language skill |
English （Business） Japanese （Fluent） |
| Foreign language competence | - |
| Working hours | Others |
| Welfares / Leave systems | |
| Assistance in visa application | - |
| Number of foreign employees | - |
Work details
Company Overview
Provide the most comprehensive drug development capabilities of any CRO worldwide.
Job Description
1. Work independently and as part of the QA team
2. Act as expert GxP consultant in relevant area
3. Train new and existing QA personnel
4. Train and educate operational staff by the development and presentation of training courses
Requirements
1. Experience in the practice of auditing, such as PMDA and other regulatory authorities, such as client audits, vendor audits, audits of clinical trial sites, etc.
2. Indispensable business level English language knowledge and experience
3. Extensive experience in quality assurance, regulatory affairs, auditing, clinical research, monitoring, data management, pharmacy, laboratory, or other relevant area, including applicable
About interview
Liaison
Auditor Manager
RGF HR Agent
900 〜 1300 ten thousand JPY
