Staff, Quality Systems & Compliance, Osaka Site (fixed Term) / 大阪工場 品質システム・コンプライアンス担当（契約社員）

Takeda

Osaka, Japan
Annual salary increase; bonus pyyment twice a year...
Business level japanese language skills
Gmp business experience in pharmaceuticals
Quality assurance documentation management
The role involves building and promoting systems to ensure the quality of sterile injectable medicines produced at the Osaka site for global distribution

Job Summary

  • The role involves building and promoting systems to ensure the quality of sterile injectable medicines produced at the Osaka site for global distribution.
  • Candidates must possess business-level Japanese language skills in speaking, writing, and reading to effectively manage quality events and document control.
  • The position offers a comprehensive benefits package including annual salary increases, twice-yearly bonuses, and flexible work styles such as telework.

Matching Summary

The role involves building and promoting systems to ensure the quality of sterile injectable medicines produced at the Osaka site for global distribution.

Salary

Annual salary increase; Bonus payment twice a year; Commutation, Housing, Overtime allowances included

Skills & Requirements

Must-have

  • Business level Japanese language skills
  • GMP business experience in pharmaceuticals
  • Quality assurance documentation management
  • Audit and inspection participation

Nice-to-have

  • English communication proficiency
  • Experience with global validation projects
  • Data integrity knowledge
  • Aseptic processing background

Key Requirements

  • University degree in Chemistry, Pharmacy, Engineering, or Biology
  • Prior GMP and Quality Assurance experience required
  • Fixed-term employment contract status

Work Rights

Not specified

Tailored Resume

Cover Letter