概要

• 給与

  -

• 業界

  Manufacturing(Pharmaceutical/MedicalEquipment)

• 仕事内容

  【Job Summary】
  - Responsible for managing the Regulatory Affairs Department
  
  【Main responsibilities
  - Lead and manage the Regulatory Affairs Department, ensuring department operations comply with legal requirements and company standards.
  - Ensure drug registration processes are completed on time and meet legal requirements.
  - Engage in building relationships with drug regulatory agencies and related organizations.
  - Develop strategies and plans to ensure efficient and expedient drug registration processes.
  - Ensure compliance with procedures and quality standards related to drug registration documents.
  - Provide creative and optimized solutions to enhance efficiency and competitiveness in drug registration processes for the company.
  
  【Company/Job Attraction】
  - Professional and friendly work environment, opportunities for career development.
  - Participation opportunities in high-quality drug registration processes.
  - Opportunities for advancement within the company and involvement in significant projects.
  - Training and enhancement of professional and management skills.