薬事部 スタッフ - Chūō
1ヶ月前
Job summary
The RA staff plans regulatory affairs activities for new and existing products.+
Responsibilities
- Interpreting regulations
- Leading cross‑functional implementation of compliance measures
- Communicating with health authorities
Qualifications:
- More than 5 years of experience in regulatory affairs- Comprehensive understanding of the Japanese PMD Act
- Demonstrated leadership and communication skills
求人説明
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