Tổng quan

• Mức lương

  -

• Ngành

  Manufacturing(Pharmaceutical/MedicalEquipment)

• Mô tả công việc

  【Job Summary】
  - Responsible for regulatory affairs activities
  
  【Main responsibilities
  - Perform tasks to ensure that the activities of the regulatory affairs department are carried out in accordance with the legal requirements of regulatory affairs regulations.
  - Ensure that the regulatory affairs process is conducted on time and meets the Company's requirements.
  - Build and maintain relationships with drug regulatory agencies and related organizations.
  - Develop and implement strategies and plans to execute the regulatory affairs process efficiently and promptly.
  - Comply with procedures and quality standards related to regulatory affairs documents.
  
  【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.