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Deputy Country Quality Head

年収:1300万 ~ 2000万

採用企業案件

採用企業

サノフィ株式会社

  • 東京都

    • 資本金500百万円
    • 会社規模501-5000人
  • その他
  • 医薬品メーカー
部署・役職名 Deputy Country Quality Head
職種
業種
勤務地
仕事内容 Key Accountabilities

Country Quality System management
Lead the implementation and maintenance of GxP quality system with respective operation units, the continues quality system implementation for competencies and related Quality documentation of GxP area: medical, pharmacovigilance, regulatory and clinical.
Deviation and CAPA management: oversight deviation and CAPA management by GxP owner functions including the subcontractor audit/ inspection findings.
Change Control management: oversight the change process which may impact GxP or health-regulated process or operations by leading multidisciplinary exchange and action plans if necessary.
Country Quality Agreement: as required ensure the valid and signed quality agreements containing quality dispositions and other mandatory quality related clause are in place.
Ensure and maintain the local computerized system inventory.

Document Management
Organize the implementation and consistent management of the country quality documentation though a global system.
Assessment of global quality documents and implementation into local operations.
Ensure required quality documents are in-place, in-use and up to date.

Country Quality Audit and Inspection
Ensure a quality oversight for all GxP functions and provide support as required during inspection or audit.
Define, implement and maintain the local key GxP subcontractor list periodically, coordinate and complete for GxP subcontractors based on the annual audit plan which are provided by the risk management criteria.
Ensure certified auditors complete the planned annual GxP audit plan in place.
Evaluate the GxP audit findings trend to define the affect the country quality system and communication with global if needed.
Evaluate new GxP subcontractors Quality Due Diligence activities before business use.

Product Alert
Manage Quality Product alerts in Japan as well ensuring operational support in case of recall in close collaboration with other stakeholders including manufacturing.

Training
Organize and manage information sharing, training sessions or programs for talent development in the division according to Sanofi standards and regulatory requirements.

Country Quality Review
Carry-out an annual Country Quality Review and organize the related meeting to present the outcomes to Country Senior Management Board

Quality Key performance indicators
Monitor and periodically report country KPIs along with global KPI indicators guideline using the global computerized system.

Non-product quality events
Escalate and inform the events occurring at the country/ global MCCQ according to Products alert team/ Local crisis management team procedure.

GQP requirement
Ensure GQP team activities along with local regulatory requirements and escalation for quality events as necessary.

Quality Culture
Enhance quality culture across the Japanese commercial entities.
応募資格

【必須(MUST)】

Your Education, Qualification & Experience

Pharmacist License
Scientific degree in science, medicine, or Pharmacy
Minimum 5 years Leadership experience in Quality at an industrial (Pharma or food is preferred) site
GxP and health-related regulations knowledge in production and development of active substances, drug product and drug device combination products as also medical devices.
Practical and solid experience of minimum 10 years in Quality System Management in health-regulated industry.
Knowledge in Auditing, Process validation, Quality Assurance, Quality Control, Regulatory Affairs, Quality Risks Management, Quality Systems domains.
Experience in Negotiation, Project Management, Networking and Problem Solving
International exposure

Your Language Skills
Japanese speaking required.
English speaking required (written & verbal)

Your Competencies
Leadership: change management, managerial courage/ fearlessly dealing with trouble Team spirit. Develop People. Transversal cooperation – customer committed
Driver of change: willing to challenge “conventional” thinking and ways of working – striving for results
Well organized, resourceful; effective and efficient at marshaling multiple resources to get things done; can work on multiple tasks at once without losing track; foresees and plans around obstacles
Stress tolerance, ability to manage critical situations.
Ability for strategic thinking and having predictions for Quality evolution.
アピールポイント 自社サービス・製品あり 外資系企業 女性管理職実績あり 従業員数1000人以上 シェアトップクラス 年間休日120日以上 産休・育休取得実績あり 教育・研修制度充実 管理職・マネージャー 完全土日休み フレックスタイム
受動喫煙対策

その他

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更新日 2024/05/08
求人番号 3513432

採用企業情報

サノフィ株式会社
  • サノフィ株式会社
  • 東京都

    • 資本金500百万円
    • 会社規模501-5000人
  • その他
  • 医薬品メーカー
  • 会社概要

    【設立年月日】2006年1月1日
    【代表者】代表取締役社長 岩屋 孝彦
    【資本金】5億円
    【従業員数】1,969名(2023年3月1日現在)*サノフィ・ジャパングループ 全体
    【本社所在地】東京都新宿区西新宿三丁目20番2号
    【その他事業所】物流センター(埼玉県三郷市、大阪府茨木市)

    【事業内容】医薬品等の製造販売・輸入、研究開発

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