JOB INFORMATION
求人情報

求人番号 75332-050

製薬・医療機器業界

外資系 メディカル

薬事マネジャー/スタッフ

  • 年収
    〜 1100万円
  • 勤務地
    東京都
  • 英語力
    中級
職務内容
Role Summary:
This position works within a team of Regulatory Affairs professionals to ensure establishes best practices in the area of pre- and post-market regulations, submissions and new product development.
Essential Responsibilities:
1. Maintains records on legislation, regulations and guidelines 2. Investigates regulatory history of similar products to assess approval implications 3. Conducts research on submission requirements and options 4. Assists in monitoring and reporting project timelines 5. Responds to RA information requests 6. Communicates license approvals when received. 7. Organizes materials from preclinical and clinical studies for review and assist in review process 8. Coordinates and assists in the preparation of submission packages for regulatory agencies 9. Assists in the review of advertising and promotional items 10. Supports regulatory inspections as required 11. Performs a broad variety of tasks in support of product and process design as assigned by the departmental manager.
応募条件
1. Minimum of 1 year experience in a regulated industry is preferred 2. Advanced degree in scientific, technology or legal disciplines 3. Statistics education and or training 4. Ability to work independently in fast-paced environment with little supervision. 5. Ability to adapt to constant change and influence positive change effectively. 6. Team-oriented and responsive to customer needs. 7. Attention to Detail and Results-Oriented. 8. Ability to understand technical documentation and execute associated procedures
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厳選求人詳細

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    アソシエイトブランドマネージャー

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  • 外資系 メディカル

    エンジニアスタッフ

    ■医療機器(整形外科手術工具)の設計・開発 ・3D CADを使用したカスタムメー...

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