Associate Director Or Principal Scientist, Facility Operations, Pharmaceutical Sciences

Takeda

Fujisawa, Japan
Not specified; bonus pyyment: twice a year; allowa...
Fluent japanese communication skills mandatory
Minimum 5 years pharmaceutical industry experience
Minimum 3 years gmp manufacturing or maintenance experience
This position is responsible for GMP manufacturing of biologics drug substances and sterile drug products for clinical trials

Job Summary

  • This position is responsible for GMP manufacturing of biologics drug substances and sterile drug products for clinical trials.
  • The role requires managing the schedule of GMP manufacturing/testing and establishing efficient strategies for engineering and maintenance.
  • Takeda offers a comprehensive benefits package including social insurance, retirement pension, and an employee stock ownership program.

Matching Summary

This position is responsible for GMP manufacturing of biologics drug substances and sterile drug products for clinical trials.

Salary

Not specified; Bonus Payment: Twice a year; Allowances: Commutation, Housing, Overtime Work etc.

Skills & Requirements

Must-have

  • Fluent Japanese communication skills mandatory
  • Minimum 5 years pharmaceutical industry experience
  • Minimum 3 years GMP manufacturing or maintenance experience
  • In-depth knowledge of plant engineering fields
  • Experience with biologics or sterile production preferred

Nice-to-have

  • English communication skill preferred
  • Experience in construction work management
  • Ability to influence at all organizational levels
  • Strategic planning for facilities control
  • Budget management for new equipment

Key Requirements

  • Business level Japanese speaking, writing, and reading
  • Minimum 1 year experience in construction or maintenance work management on-site
  • Degree in Pharmacy, Chemistry, Biology, Engineering or related field
  • Knowledge of international regulatory requirements for pharmaceutical industry

Work Rights

Not specified

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