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CMC薬事マネージャー// CMC RA manager

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外資系老舗製薬会社にてCMC薬事マネージャーの募集です。臨床試験段階におけるCTN、CIB、機構相談(品質)資料の作成等を担っていただきます。製薬企業における薬事・CMC関連部署での経験をお持ちの方にご活躍いただけます。勤務地は兵庫県となります。

職務内容:

  • 開発段階から市販後まで、CMC関連の薬事業務(臨床試験段階におけるCTN・CIB、機構相談(品質)資料の作成等)
  • 医薬品承認申請(CMC申請戦略の策定、CTD・承認申請書の作成・照査)
  • 医療機器承認・認証申請(CMC申請戦略の策定、STED・承認申請書の作成・照査)
  • 製造業許可・外国製造業者認定対応
  • GMP調査の当局対応窓口業務
  • 市販後のメンテナンス

必須要件:

  • 製薬企業における薬事・CMC関連部署、または品質保証部門での勤務経験
  • コミュニケーションレベルの日本語力
  • ビジネスレベル英語力(TOEIC700点)
  • 日本での就労資格

歓迎要件:

  • グローバル環境での業務経験
  • 海外事業所との協働経験
  • 製薬業界におけるCMC薬事の経験
  • 薬事規制に基づいた承認申請資料作成の経験
  • CMC領域における高い専門性・知識
  • 申請および市販後のCMC関連薬事規制に関する知識

会社概要:

外資系老舗製薬会社。世界トップレベルの新薬を創出しており、業界のリーディングカンパニーとしても知名度が高い企業です。外資系らしい風通しの良い環境で、社内でのトレーニング制度がしっかりしているのが特長です。

求人番号: Y3WIUS

Contract Type: Perm

Specialism: Healthcare

Focus: Regulatory Affairs

Industry: Pharmaceuticals

Salary: ¥8,000,000 - ¥14,000,000 per annum

Workplace Type: On-site

Experience Level: Mid Management

Language: Japanese - Basic

Second Language: English - Business level

Location: Hyogo

Job Reference: Y3WIUS-D3818C72

Date posted: 20 April 2026

Consultant: Yota Fujimura