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Senior Manager, Global Development Quality Lead – Japan

Morunda K.K.
Posted 11 days ago, valid for 9 days
Location

Chuo City, Tokyo

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The role involves leading quality and compliance activities in GCP, GVP, Medical Affairs, and Regulatory Affairs for the Japan affiliate.
  • Candidates should have a Bachelor's degree and at least 8 years of relevant experience in the pharmaceutical or healthcare industry.
  • The position offers a salary that reflects the seniority and expertise required for managing complex quality and compliance issues.
  • Key responsibilities include providing strategic quality guidance, managing quality issues, and mentoring junior team members.
  • The role provides an opportunity to work in a hybrid model in Tokyo, contributing to the enhancement of quality systems and compliance.

Key Responsibilities

  • Lead quality and compliance activities across GCP, GVP, Medical Affairs, and Regulatory Affairs for the Japan affiliate
  • Provide strategic quality guidance and drive risk-based quality initiatives, including audits
  • Lead and support inspection readiness and preparation for local operations
  • Identify and drive process improvements aligned with quality objectives
  • Manage quality issues and ensure appropriate escalation of significant non-compliance
  • Provide expert guidance and training on international regulations and company quality standards
  • Partner with local and global stakeholders to strengthen the quality management system
  • Coach and mentor junior team members and/or take ownership of key quality processes


Requirements

Ideal Background

  • Bachelor's degree or equivalent experience
  • 8+ years of relevant experience in the pharmaceutical or healthcare industry
  • Strong knowledge and practical application of GCP and/or GVP
  • Background in quality/compliance or clinical development, with solid GCP/GVP expertise
  • Experience managing complex quality and compliance issues
  • Experience in training, supervision, line management, or staff development
  • Strong project management, planning, and prioritization skills
  • Experience with risk-based quality management and process improvement
  • Strong communication and stakeholder management skills, including the ability to influence senior stakeholders
  • Strong analytical, problem-solving, and collaborative skills


Benefits

Why Join?

  • Join a fast-growing global biopharmaceutical company with an innovative pipeline
  • Take on a senior, high-visibility quality leadership role within the Japan affiliate
  • Gain broad exposure across GCP, GVP, Medical, and Regulatory Affairs
  • Work closely with global and Japan stakeholders in an international environment
  • Play a key role in strengthening quality systems, inspection readiness, and compliance
  • Opportunity to influence strategic quality initiatives and process improvements
  • Hybrid working model in Tokyo
  • Opportunity to develop and mentor others while continuing to grow as a quality leader





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