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ヘルスケア

Safety Manager, QMS

検索に戻る 今すぐ応募
求人公開日:   2026/09/29

雇用形態

正社員

業種

Medical Device

職種

Pharmacovigilance

給与

7,500,000 円 年収 ~ 19,000,000 円 年収 経験考慮の上、応相談
Market range: 7.3M–14.7M JPY base + 10% bonus (16.17M JPY all-inclusive at top of range). Original posting listed base pay as N/A.

必須言語

英語: 流暢
日本語: 流暢

勤務地

東京

ビザ

就労ビザが必要となります

求人情報

Role: Safety Manager, QMS

What you'll do

  • Execute and maintain Good Vigilance Practices (GVP) and Post-Market Surveillance (PMS) activities in compliance with Japanese regulatory requirements.
  • Conduct periodic safety information collection, review, and assessment required for PMS.
  • Prepare and submit vigilance reports (e.g., E2B reports) to regulatory authorities as required.
  • Register and maintain product legal labeling, including electronic Package Insert (ePI) and Unique Device Identification (UDI), in Japanese regulatory authority databases (MHLW and PMDA).
  • Coordinate with global Quality Assurance and Vigilance teams to ensure alignment in PMS reporting and processes.
  • Conduct GVP annual training and self-inspection to remain compliant with QMS and GVP ordinances as a Marketing Authorization Holder (MAH) in Japan.
  • Manage suppliers related to GVP operations (e.g., case processing, translation services).
  • Maintain documentation required for QMS and GVP compliance, including SOPs and audit readiness materials.
  • Support QMS and GVP-related audits and inspections.
  • Identify and support implementation of QMS and PMS process improvements.

Location: Tokyo, Japan

応募資格

Must-haves

  • BS in a related scientific field or equivalent.
  • Minimum 5 years of experience in Vigilance or Quality Assurance in Pharma, IVD, or Medical Device industry.
  • Experience in GVP and PMS activities in Japan.
  • Experience interacting with MHLW, PMDA, or relevant regulatory authorities in vigilance and PMS areas.
  • Ability to work in a matrix and global environment.
  • Experience and knowledge of the database of Japanese regulatory authorities (MHLW and PMDA).
  • Strong organizational skills and attention to detail.
  • Ability to work independently as well as in a team environment.
  • Proficient in Microsoft Office (Word, Outlook, Excel, PowerPoint).
  • Fluent in Japanese and fluent in English.

Salary: Negotiable

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