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PQQIアソシエイトディレクター/ PQQI Associate Director

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An international pharmaceutical company is seeking an Associate Director, Product Quality & Quality Information (PQQI). The selected candidate will lead product quality and quality information functions, ensuring compliance, operational excellence, and cross-functional alignment across the full product lifecycle. This is a hybrid setup role.

Responsibilities:

  • Define and execute the strategic direction of the Product Quality & Quality Information function aligned with Japan QA strategy
  • Lead and manage the PQQI team including Product Quality and Quality Information leaders while ensuring effective GQP operations
  • Drive organisational integration across PQ and QI functions to improve quality outcomes and operational efficiency
  • Oversee performance management, talent development, resource allocation, and capability building within the team
  • Ensure GQP, QMS, GMP, and GDP compliance across product lifecycle activities including product release and complaint management
  • Maintain inspection readiness and support PAI and GMP inspections across manufacturing, packaging, and supply sites
  • Establish and maintain SOPs and quality systems in compliance with applicable pharmaceutical regulations and corporate standards
  • Manage product release processes and review changes and deviations in line with GQP requirements
  • Drive process simplification and continuous improvement across quality information and complaint handling systems
  • Monitor quality metrics and ensure timely, accurate quality reporting to internal and external stakeholders
  • Collaborate with global and local teams including QA, regulatory, manufacturing, and call centre functions
  • Ensure readiness for new product launches and provide quality input during development and pre-launch phases

Requirements:

  • Bachelor’s degree or above in pharmacy, chemistry, biology, engineering, or related health science field
  • More than 5 years of experience in GQP, QMS, GMP, or GDP quality operations within the pharmaceutical industry
  • Experience in a leadership role within regulated pharmaceutical quality environments
  • Strong knowledge of GQP, QMS, GMP, GDP, and related corporate quality standards
  • Strong cross-functional leadership and stakeholder management experience in global organisations
  • Proficient in English and Japanese

Preferred requirements:

  • Advanced degree in pharmacy, chemistry, biology, engineering, or related field
  • Experience in marketing affiliate quality operations and sourcing site management

About the Company:

A global pharmaceutical organisation focused on innovative medicines and healthcare solutions across major therapeutic areas. The company operates internationally with a strong commitment to scientific advancement, quality, and patient outcomes.

Keywords:

品質保証, 製品品質, 品質管理, 医薬品, 規制対応, 求人, 外資系

Job Ref: OZJB65

Contract Type: Perm

Specialism: Healthcare

Focus: Quality Assurance

Industry: Pharmaceuticals

Salary: ¥10,000,000 - ¥25,000,000 per annum

Workplace Type: Hybrid

Experience Level: Director

Language: Japanese - Professional working

Second Language: English - Business level

Location: Hyogo

Job Reference: OZJB65-0267ACE1

Date posted: 15 May 2026

Consultant: Yota Fujimura