Greater Tokyo Area Randstad Japan

・事業部門の方針に沿った部門目標を設定し、達成をリードする。

・部門の生産性向上とリソース最適化を推進する。

・規制政策・インテリジェンスに関し、社内外を調整・主導できる人材を育成する。

・社内(日本およびグローバル)へ、価値ある規制政策・インテリジェンスを迅速に提供し、事業影響を分析する。

・プロジェクトチームに対し、規制政策・インテリジェンスの専門的アドバイスを行う。

・厚労省、PMDA、業界団体などへ提出する規制政策・インテリジェンス関連の回答作成を主導する。

・Japan Regulatory Affairs Leadership の一員として部門全体を牽引する。

【求められる経験・スキル / Required Experience And Skills】
・開発薬事のご経験(8-10年程度)※規制や当局対応に詳しい方

・マネジメント経験(あれば尚良し)

【学歴】
大学卒業以上

【職種 / type of occupation】
薬事、メディカルライティング

【給与 / salary】
年収 1,300 〜 2,000万円

【賞与】
【雇用形態 / employment status】
正社員

雇用期間

期間の定めなし

【就業時間 / working hours】
09:00~18:00

【休日休暇 / holiday】
土曜日 日曜日 祝日

【保険 / social insurance】
健康保険 厚生年金保険 雇用保険

受動喫煙防止措置

敷地内禁煙

【特長 / features】
女性活躍中, 上場企業, 外資系企業, フレックスタイム制, 完全週休2日制, 土日祝休み, グローバル人材歓迎

【業種 / industry】
医療機器・医療品関連

※詳細はお仕事のご紹介時にお伝えします

Job ID: VAC-284455/



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