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CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
Hiring Company | 大塚製薬株式会社 |
Location | Tokushima Prefecture |
Job Type | Permanent Full-time |
Salary | 6 million yen ~ 12 million yen |
【求人No NJB2186366】
【業務内容】
アジア・アラブ諸国等における開発段階から承認申請・承認取得,及び承認後のCMC薬事業務全般をご担当いただきます。
・CMC薬事戦略策定
・CMC申請資料及び製造所登録/更新資料の作成と規制当局からの照会事項対応(現地作成の品質資料のレビューを含む)
・承認後の薬事変更に関する薬事影響評価・承認後変更申請対応
Minimum Experience Level | No experience |
Career Level | Mid Career |
Minimum English Level | Business Level |
Minimum Japanese Level | Native |
Minimum Education Level | Bachelor's Degree |
Visa Status | Permission to work in Japan required |
Job Type | Permanent Full-time |
Salary | 6 million yen ~ 12 million yen |
Work Hours | 09:00 〜 17:30 |
Holidays | 【有給休暇】1ヵ月目より、10〜最大20日付与(前職の社歴により、日数が変わります) 【休日】完全週休二日制 土 日 祝日 夏… |
Industry | Pharmaceutical |