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【AstraZeneca】【QA】Senior Compliance Specialist/Compliance Specialist, Quality Assurance

Location Maihara, Shiga, Japan Job ID R-194340 Date posted 25/03/2024

■ 職務内容 / Job Description

GMP/GQPに関連する品質保証業務全般
①国内&グローバルの要件に準拠した品質マネジメントシステムの維持管理
②グループ内製造所との連携による強固なプロセスの構築・標準化
③品質改善計画、新製品導入などのプロジェクトのリード・参画

■ 応募資格(経験、資格等)/ Qualification (Experience & Skill etc.)

【経験 / Experience】

<必須 / Mandatory>

医薬品の品質保証 、製造/品質管理 、生産技術等の実務経験

<歓迎 / Nice to have>

cGMP及びICHガイドライン知識、薬事関連知識
英語によるビジネスコミュニケーション経験(会議)

【資格 / License】

<歓迎 / Nice to have>

薬剤師資格

【能力 / Skill-set】

<必須 / Mandatory>

プロジェクトマネジメントスキル
高いコミュニケーション能力とリーダーシップ

<歓迎 / Nice to have>

Operartional Excellenceに関する知識・実務経験

【語学 / Language】

<必須 / Mandatory>

日本語 Japanese:ネイティブレベル

英語 English:ビジネスレベル(要:英会話能力、英語での会議あり)

【キャリアレベル / Career Level】

C

【勤務地 / Work Location】

Maihara, Japan

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

10000095 C QAMM

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Glassdoor logo Rated four stars on Glassdoor

Great culture, great work assignments, supportive management. Rotation opportunity within the company. They value inclusion and diversity.