QA (Sr. MGR)
外資系製薬企業
想定年収
800万円 ~ 1,300万円
勤務地
東京都
仕事内容
・The role acts as a deputy to the Quality Assurance Officer and supports overall quality oversight.
・Manages multiple areas of the Quality Management System (QMS) within commercial quality operations.
・Responsible for establishing effective work methods, operational excellence, and cost management.
・Serves as a project lead within the function or a core member of cross‑functional initiatives.
・Leads or contributes to high‑visibility projects involving senior management.
・Maintains and continuously enhances the QMS in alignment with regulatory requirements and global standards.
・Provides expert guidance on interpretation and application of GQP, GMP, and GDP regulations.
・Applies advanced statistical analysis and continuous‑improvement methodologies to enhance quality performance.
・Independently develops new approaches to support data‑driven and strategic decision‑making.
・Builds strong partnerships with stakeholders across supply chain, regulatory, quality, manufacturing, and safety functions.
・Supports Quality Management Reviews and activities of the Quality Head.
・Supports all quality assurance activities as deputy, including deviations, change control, training, audits, and recalls.
・Oversees documentation management, training programs, and document coordinator qualification.
・Reviews manufacturing and quality data and authorizes final product release.
・Ensures quality compliance across contractors, logistics providers, and distributors.
・Leads investigations, CAPA activities, audits, regulatory inspections, and interactions with health authorities.
募集人数
1人
応募条件
技能/経験
■Typical Education & Experience
・10+ years of QA relevant experience in the pharmaceutical industry and a Master of Science.
・5+ years of QA relevant experience with Quality Management System
・Experience with Electronic Document Management Systems or other GxP applications.
・Experience in Project Management for Launch, site transfer and analytical transfer.
・Experience in GMP compliance inspections, FMA and Conformity check.
・Experience in analytical, process chemistry and/or formulation development.
■Knowledge & Skills
・Excellent Japanese and English business communication skills.
・Demonstrates in-depth knowledge of PMD. Act (薬機法), GMP, GQP and GDP.
・Demonstrates in-depth knowledge of QA principles, concepts, industry practices, and standards.
・Demonstrates knowledge of Information Systems Technology, understanding of Computer System Validation (CSV) including current electronic records and signature requirements.
学歴
大学院(修士)
職務経験
要 (5年以上)
業界経験
要
年齢
年齢制限不問
英語力
中級以上
その他語学力
語学力詳細
ー
勤務条件
雇用形態
無期雇用
試用期間
有り(4ヶ月)
給与
年俸制
年収:800万円 ~ 1,300万円
月収:61万円~
月額基本給:61万円~
賞与・インセンティブ
年1回
詳細は担当コンサルタントにお問い合わせください
別途RSU付与
昇給
有り 年1回
※オファー時に詳細をお伝えします
勤務地
東京都
就業時間
09:00~18:00
休憩時間:1h
残業:月10時間~40時間程度
管理監督職
残業手当
その他
管理監督職のため、労働基準法41条により、労働時間、休憩、休日の割増賃金の規定は適用されません。
通勤手当
交通費:全額支給(社内規定に基づいて支給)
休日・休暇
完全週休二日制, 土, 日, 祝日, 年末年始
年間休日:125
年間有給休暇:初年度最大12日 1か月目から付与
※入社月により、初年度付与日数は変動します
社会保険
雇用保険, 健康保険, 労災保険, 厚生年金
求人No.:NJB2376554
最終更新日:2026/7/13
