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Deadline | May 31st, 2025 |
Hiring Company | インターナショナル・ケミカル・エンティティ・ジャパン株式会社 |
Location | Fukushima Prefecture, Iwaki-shi |
Job Type | Permanent Full-time |
Salary | 3.5 million yen ~ 4.5 million yen |
品質管理業務担当(試験員)(医薬品原薬と中間体の製造業における品質管理)- Quality Control Operations (Examiner) (Manufacturing API)
・原材料、中間体、中間製品および製品の試験検査
・試験設備の点検、整備、保全、校正、記録保管
・規格及び試験法・規制文書の作成、改訂
Minimum Experience Level | Over 1 year |
Career Level | Mid Career |
Minimum English Level | Basic (Amount Used: English usage about 25%) |
Minimum Japanese Level | Fluent |
Minimum Education Level | Bachelor's Degree |
Visa Status | Permission to work in Japan required |
必須条件 (Requirement)
医薬品関係企業でGMPにかかわる業務経験を有していると業務への理解が早まります。
優遇 (Preferred skills/knowledge/experiences)
・化学分析機器(HPLC、GCなど)が操作できる方
・英語での会話(メール含む)ができる方、英語の文献が読めて和訳できる方は優遇
・工場などの品質検査又はそれに類する経験がある方優遇
・薬剤師資格保有者は優遇
・危険物取扱者は優遇(応募時に資格を保有していなくても可 - ない方は入社後取得して頂きます)
Job Type | Permanent Full-time |
Salary | 3.5 million yen ~ 4.5 million yen |
Salary Bonuses | Bonuses included in indicated salary. |
Work Hours | 8:30 - 17:15, 7 hours 15 minuites, 1 hour break in the middle |
Holidays | Saturdays and Sundays, National Holidays |
Job Division | Quality and Regulatory Affairs Division(品質・薬事本部、品質管理部) |
Industry | Pharmaceutical |
Company Type | Small/Medium Company (300 employees or less) - International Company |
Non-Japanese Ratio | Majority Japanese |