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  3. ブリストル・マイヤーズ スクイブ株式会社:Senior Manager, External Manufacturing Quality, Cell Therapy Global Qualityの求人情報詳細

Senior Manager, External Manufacturing Quality, Cell Therapy Global Quality

ブリストル・マイヤーズ スクイブ株式会社
  • 課長以上
  • 外資系企業

想定年収

1,000万円 ~ 1,500万円

勤務地

東京都

仕事内容

■Position Summary

Provide Quality Oversight of technology transfer and routine GCTP/GMP operations at CMOs in support of cell therapy intermediate product manufacturing.

Partner with CMO Quality to provide oversight of manufacturing operations and ensure work is performed in accordance with approved regulatory submissions, master service and/or quality agreements and applicable regulatory requirements.



■Duties/Responsibilities
・Provide Quality Oversight of technology transfer and routine GCTP/GMP operations at CMOs in support of cell therapy intermediate product manufacturing.
・Partner with CMO Quality to provide oversight of manufacturing operations and ensure work is performed in accordance with approved regulatory submissions, master service and/or quality agreements and applicable regulatory requirements.
・Provide quality compliance guidance and oversee readiness for pre-license inspection including the remediation of any GCTP/GMP deficiencies in order to ensure a timely approval and commercial launch
・Collaborate with other leaders across the organization and assist in the continuous improvement and lifecycle management of CMO oversight program
・Responsible for batch record review and product batch disposition
・Responsible for review and/or approval of CMO deviation investigations, CAPA, controlled documents (Master Batch Records)
・Act as QA impact assessor and approver of CMO related changes
・Responsible for review and approval of protocol/reports in support of regulatory submissions
・Responsible for review and/or approval of COI risk assessment and process map
・Responsible for quality risk assessment
・Develop and approve annual product review reports generated by CMOs
・Collaborate with Global Quality Systems and ensure CMO’s timely implementation of corrective actions resulted from BMS’s audits
・Assist in CMO GCTP/GMP audits, as required
・Influencing to key stakeholders internally and externally.
・Support Management Review activities and oversee trending of key quality, product and GCTP/GMP metrics related to CMO
・Develop departmental goals and ensure timely completion of all deliverables

■Reporting Relationship
Director, APAC External Manufacturing Quality, Cell Therapy

募集人数

1人

応募条件

技能/経験

■Qualifications
Specific Knowledge, Skills, Abilities:
・Expertise in GCTP/GMP compliance and Japan regulations is required
・Background in aseptic processing is required
・Demonstrates strong proficiency in both Japanese and English communication skills.
・Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships
・Soft skills such as logical thinking and agility are required
・Ability to work in a fast-paced environment

■Education/Experience/ Licenses/Certifications:
Master’s or bachelor’s in biochemistry, biology, microbiology, chemistry, engineering, pharmacy, or a related field.
Experience with overseeing GCTP/GMP operations is preferred

■Travel
This position requires travel to CMO

学歴

大学

職務経験

(5年以上)

業界経験

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

勤務条件

雇用形態

無期雇用

試用期間

有り(3ヶ月)

給与

年俸制

年収:1,000万円 ~ 1,500万円

月収:83万円~125万円

月額基本給:83万円~125万円

※詳細はオファー時にご説明いたします

賞与・インセンティブ

年1回  昨年実績:あり

昇給

有り 年1回 / 4月

勤務地

東京都

就業時間

09:00~17:15

休憩時間:60分

残業:月10時間~30時間程度

管理監督職
※残業時間はあくまで目安となります

残業手当

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

休日・休暇

完全週休二日制, 年末年始

年間休日:122

年間有給休暇:有給休暇は試用期間満了後から付与されます
( 有給休暇:初年度は試用期間終了後から1~10日付与(入社時期によって初年度の付与日数は異なります) )
【休日・休暇詳細】
日曜日、土曜日、国民の祝日、年末、年始、会社創立記念日(7月1日)、その他会社があらかじめ休日とした指定した日

社会保険

雇用保険, 健康保険, 労災保険, 厚生年金

求人No.:NJB2382315

最終更新日:2026/5/21

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  3. ブリストル・マイヤーズ スクイブ株式会社:Senior Manager, External Manufacturing Quality, Cell Therapy Global Qualityの求人情報詳細